ArticlePDF AvailableLiterature Review

Abstract and Figures

Mental imagery is an experience like perception in the absence of a percept. It is a ubiquitous feature of human cognition, yet it has been relatively neglected in the etiology, maintenance, and treatment of depression. Imagery abnormalities in depression include an excess of intrusive negative mental imagery; impoverished positive imagery; bias for observer perspective imagery; and overgeneral memory, in which specific imagery is lacking. We consider the contribution of imagery dysfunctions to depressive psychopathology and implications for cognitive behavioral interventions. Treatment advances capitalizing on the representational format of imagery (as opposed to its content) are reviewed, including imagery rescripting, positive imagery generation, and memory specificity training. Consideration of mental imagery can contribute to clinical assessment and imagery-focused psychological therapeutic techniques and promote investigation of underlying mechanisms for treatment innovation. Research into mental imagery in depression is at an early stage. Work that bridges clinical psychology and neuroscience in the investigation of imagery-related mechanisms is recommended. Expected final online publication date for the Annual Review of Clinical Psychology Volume 12 is March 28, 2016. Please see http://www.annualreviews.org/catalog/pubdates.aspx for revised estimates.
Content may be subject to copyright.
CP12CH10-Holmes ARI 12 February 2016 15:47
Mental Imagery in Depression:
Phenomenology, Potential
Mechanisms, and Treatment
Implications
Emily A. Holmes,1,2Simon E. Blackwell,1
Stephanie Burnett Heyes,3,4Fritz Renner,1
and Filip Raes5
1Medical Research Council Cognition and Brain Sciences Unit, Cambridge CB2 7EF, United
Kingdom; email: emily.holmes@mrc-cbu.cam.ac.uk, simon.blackwell@mrc-cbu.cam.ac.uk,
fritz.renner@mrc-cbu.cam.ac.uk
2Department of Clinical Neuroscience, Karolinska Institutet, Stockholm 171 77, Sweden
3School of Psychology, University of Birmingham, Birmingham, West Midlands B15 2TT,
United Kingdom; email: s.burnettheyes@bham.ac.uk
4Department of Experimental Psychology, University of Oxford, Oxford OX1 3UD,
United Kingdom
5Faculty of Psychology and Educational Sciences, University of Leuven, 3000 Leuven, Belgium;
email: filip.raes@ppw.kuleuven.be
Annu. Rev. Clin. Psychol. 2016. 12:249–80
First published online as a Review in Advance on
January 15, 2016
The Annual Review of Clinical Psychology is online at
clinpsy.annualreviews.org
This article’s doi:
10.1146/annurev-clinpsy-021815-092925
Copyright c
2016 by Annual Reviews.
All rights reserved
Keywords
intrusive imagery, vividness, overgeneral memory, rescripting, optimism
Abstract
Mental imagery is an experience like perception in the absence of a percept.
It is a ubiquitous feature of human cognition, yet it has been relatively ne-
glected in the etiology, maintenance, and treatment of depression. Imagery
abnormalities in depression include an excess of intrusive negative mental im-
agery; impoverished positive imagery; bias for observer perspective imagery;
and overgeneral memory, in which specific imagery is lacking. We consider
the contribution of imagery dysfunctions to depressive psychopathology and
implications for cognitive behavioral interventions. Treatment advances cap-
italizing on the representational format of imagery (as opposed to its con-
tent) are reviewed, including imagery rescripting, positive imagery genera-
tion, and memory specificity training. Consideration of mental imagery can
contribute to clinical assessment and imagery-focused psychological thera-
peutic techniques and promote investigation of underlying mechanisms for
treatment innovation. Research into mental imagery in depression is at an
early stage. Work that bridges clinical psychology and neuroscience in the
investigation of imagery-related mechanisms is recommended.
249
Click here to view this article's
online features:
Download figures as PPT slides
Navigate linked references
Download citations
Explore related articles
Search keywords
ANNUAL
REVIEWS
Further
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Contents
INTRODUCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 250
MentalImagery ................................................................ 250
Depression..................................................................... 251
WhyInvestigate MentalImagery inDepression?................................. 252
MENTAL IMAGERY IN DEPRESSION AND OTHER DISORDERS . . . . . . . . . . . . 253
Intrusive, Emotional Mental Imagery Across Psychological Disorders . . . . . . . . . . . . . 253
What Does Dysfunctional Mental Imagery Look Like in Depression? . . . . . . . . . . . . . 253
Do Imagery Dysfunctions Play a Role in the Onset or Maintenance
ofDepression? .............................................................. 259
Taking a Developmental Perspective on Mental Imagery in Depression . . . . . . . . . . . 261
Does Adaptive Mental Imagery Contribute to Resilience?. . . . . . . . . . . . . . . . . . . . . . . . . 261
MODIFYINGMENTAL IMAGERY IN DEPRESSION .......................... 262
Implications of Mental Imagery for Cognitive Behavioral Interventions
inDepression ............................................................... 262
MECHANISMSOF MENTAL IMAGERY INDEPRESSION .................... 266
Can Investigating Mental Imagery Help Us Better Understand the Mechanisms
UnderlyingDepression?..................................................... 266
CONCLUSIONS................................................................. 269
INTRODUCTION
Mental Imagery
Definition and some history. Mental imagery allows us to relive the past, prelive the future,
and make decisions, comprising a key part of our everyday mental life. It involves seeing with the
mind’s eye, hearing with the mind’s ear, and so forth (Kosslyn et al. 2001), that is, mental imagery is
an experience like perception but in the absence of a percept. Evidence indicates that in many ways
mental imagery is like “weak perception” (Pearson et al. 2015). It is part of our autobiography—
memories from our childhood can flash back to mind as vivid sensory imagery (e.g., a scene from
the first day at school). We can also simulate future events (e.g., an upcoming holiday). Yet despite
its centrality, the study of mental imagery has seen more fluctuation in scientific respectability
than almost any other aspect of cognitive psychology (Baddeley & Andrade 2000). The equivalent
might be said about its therapeutic application (Edwards 2007). It is perhaps no wonder then that
mental imagery has been relatively neglected, both in the etiology and maintenance of depression
and in terms of its implications for psychological treatment.
To move forward, it can help to look back. Mental imagery was studied in the early days of
psychology by Galton (1883), who began by investigating individual differences in imagery ability.
In “cases where the faculty is very high,” mental imagery was described as brilliant or dazzling,
e.g., “thinking of the breakfast table this morning, all the objects in my mental picture are as
bright as the actual scene” (Galton 1883, p. 62; see also sidebar, Imagine Your Breakfast Table).
In “cases where the faculty is at the lowest,” participant reports included, “I recollect the breakfast
table but do not see it” (p. 64). Galton notes the challenges to mental imagery as a subject of
scientific inquiry, observing at the onset of his investigations that those research participants who
were scientists “looked on me as fanciful and fantastic” and “had no more notion of its [mental
imagery’s] true nature than a color-blind man” (p. 58). His writing also includes observations
250 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
IMAGINE YOUR BREAKFAST TABLE
The following is adapted from Galton (1883).
Think of some definite object—suppose it is your breakfast table as you sat down to it this morning—and consider
carefully the picture that rises before your mind’s eye.
1. Illumination: Is the image dim or fairly clear? Is its brightness comparable to that of the actual scene?
2. Definition: Are all the objects pretty well defined at the same time, or is the place of sharpest definition at any
one moment more contracted than it is in a real scene?
3. Coloring: Are the colors of the china, of the toast, bread-crust, mustard, meat, parsley, or whatever may have
been on the table, quite distinct and natural?
Below are some of the comments received by Galton—which of these is closest to your experience?
1. High imagery ability: “The mental image appears to correspond in all respects with reality. I think it is as clear
as the actual scene.”
2. Mediocre imagery ability: “Fairly clear as a general image; details rather misty.”
3. Low imagery ability: “My powers are zero. To my consciousness there is almost no association of memory with
objective visual impressions. I recollect the breakfast table but do not see it.”
that mental imagery can be associated with psychopathology—it “supplies the material out of
which dreams and the well-known hallucinations of sick people are built” (p. 58). He describes
an example in which imagery appears to create difficulties in giving a speech: “One statesman has
assured me that a certain hesitation in utterance which he has at times, is due to his being plagued
by the image of his manuscript speech with its original erasures and corrections. He cannot lay
the ghost, and he puzzles in trying to decipher it” (p. 67). This is an example of one type of the
intrusive negative images associated with psychopathology; we argue that such negative images
are also associated with depression.
Imagery and perception draw on shared neural mechanisms, and mental imagery is distinct from
verbal language (Kosslyn et al. 2001, Pearson et al. 2015). This distinction between imagery and
verbal language is an important one for therapy: The content of a thought is what information it
conveys, whereas the format is the nature of the code used to represent this information. We think
in multiple ways. Thus, we can think by using picture-like depictive formats (mental images) in
addition to language-like descriptive formats (verbal thoughts). Although all formats of a patient’s
thoughts deserve investigation, in clinical assessment imagery is often neglected and the focus
instead is on verbal thoughts.
If we return to Galton’s observations, although individuals with depression may do equally
well as their nondepressed counterparts at conjuring up an image of their usual breakfast table, we
suggest that depressed individuals would typically do less well if asked to recall a particular (e.g.,
most recent birthday) breakfast table, that is, they may struggle to generate imagery of a specific
memory. Further, we suggest that individuals with depression may have particular difficulties with
generating vivid and compelling imagery of positive events. Negative memories and images, in
contrast, may come to mind all too readily.
Depression
Definition. The Diagnostic and Statistical Manual of Mental Disorders (DSM-5; Am. Psychiatr.
Assoc. 2013) defines major depressive disorder (MDD) as a potential diagnosis when someone
experiences one or more major depressive episodes. To meet criteria for a major depressive episode,
www.annualreviews.org Mental Imagery in Depression 251
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
individuals must experience five or more symptoms for at least two weeks, to the extent that they
suffer clinically significant distress or impairment. These symptoms must include at least one of the
two core symptoms of depression: depressed mood and markedly diminished interest or pleasure
in activities (anhedonia). Other possible symptoms include significant weight changes or changes
in appetite; insomnia or hypersomnia; psychomotor agitation or retardation; fatigue or loss of
energy; feelings of worthlessness or excessive or inappropriate guilt; diminished ability to think
or concentrate, or indecisiveness; and recurrent thoughts of death, suicidal ideation, or a suicide
attempt.
Global burden and current statistics. Depression is common, with lifetime prevalence esti-
mates ranging from 16.6% (Kessler et al. 2005) to 30% for men and 40% for women (Andrews
et al. 2005). Correspondingly, depression is a leading cause of global disease burden, with recent
estimates placing it second among all illnesses in terms of years lived with disability (Vos et al.
2012). Depression also commonly co-occurs with chronic physical health problems such as angina
and diabetes and contributes to significantly worse outcomes (Moussavi et al. 2007). Psycholog-
ical and pharmacological interventions for depression appear equally effective in meta-analyses
(Cuijpers et al. 2013), although when compared directly, some evidence indicates that psycholog-
ical treatment has a longer-lasting impact than pharmacological treatment (Hollon et al. 2006).
However, approximately 50% of patients with depression do not respond to treatment (Cuijpers
et al. 2014, Hollon et al. 2006). In addition, about half of those who suffer a first episode will ex-
perience a second, and after three episodes, the risk of further episodes is 90% (see, e.g., Bockting
et al. 2015). Given the global scale of depression and limits of current treatments, there is a great
and urgent need for treatment innovations of all sorts, including psychological treatments.
Why Investigate Mental Imagery in Depression?
There are three key reasons why we need to consider mental imagery in depression. One is to
more fully understand the mental landscape of patients in a clinical assessment. The second is to
make more effective use of psychological therapy, that is, to use imagery as well as verbal tech-
niques. The third is to learn more about the cognitive and neural mechanisms underlying the
relationship between mental imagery and depression and to use this information to aid future
treatment innovation.
Imagery has been relatively neglected in both assessment and therapy for depression. The
translation of cognitive models into clinical practice in cognitive behavioral therapy (CBT) has
included a focus on negative automatic (verbal) thoughts (Beck et al. 1979); on rumination (“be-
haviors and thoughts that passively focus one’s attention on one’s depressive symptoms and on
the implications of these symptoms”; Nolen-Hoeksema 1998, p. 239), which is a predominantly
verbal process (Fresco et al. 2002); and on the phenomenon of overgeneral memory (OGM) when
asked to deliberately recall events (Williams et al. 2007) in informing mindfulness. All such work
has led to great strides in CBT for depression—a leading treatment (e.g., Natl. Inst. Health Clin.
Excell. 2009). However, additionally incorporating a greater focus on imagery in clinical practice
may have advantages, opening the doors to wider information than is obtained by just asking about
verbal thoughts. Indeed, we now know that thoughts based on sensory imagery are common in
depression (e.g., Moritz et al. 2014), and these represent a potential, and additional, treatment
target.
Mental imagery is essential to our mental life, enabling us to remember the past, simulate and
pre-experience the future, and make decisions (Schacter et al. 2012). Almost any behavior that
might gain from sensory simulation may use mental images, from avoiding threats (e.g., failures)
252 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
or seeking rewards (e.g., future successes) to solving problems and completing tasks (e.g., everyday
activities). Thus, disruptions to imagery-based representations of emotional information in any of
these areas may be important in understanding and treating emotional disturbance in depression.
MENTAL IMAGERY IN DEPRESSION AND OTHER DISORDERS
Intrusive, Emotional Mental Imagery Across Psychological Disorders
Although it may generally be advantageous to clearly remember the details of past situations
when confronted with reminders, in psychopathology intrusive, emotional mental imagery of
past negative events can become overwhelming and uncontrollable, driving the maintenance of a
disorder within a cognitive therapy formulation. The past decade has seen a proliferation of
studies grounded in CBT examining intrusive, emotional mental images across a wide range of
psychological disorders (special journal issues include Hagenaars & Holmes 2012, Holmes &
Hackmann 2004, Holmes et al. 2007a, Krans 2011, Stopa 2011).
Negative intrusive memories of traumatic events comprise the hallmark feature of posttrau-
matic stress disorder (PTSD; Am. Psychiatr. Assoc. 2013), and such imagery is core to its successful
assessment and treatment (Natl. Inst. Health Clin. Excell. 2005, 2013). Images of oneself perform-
ing badly in social situations (see the previous example from Galton of the statesman’s speech)
have been shown to be causal in social phobia (Hirsch et al. 2003), and imagery techniques are
key in its treatment (Wild et al. 2007). Intrusive imagery has been reported in eating disorders,
obsessive-compulsive disorder, spider phobia, body dysmorphic disorder, schizophrenia, bipolar
disorder, and so forth (for examples, see Hagenaars & Holmes 2012, Holmes & Hackmann 2004,
Holmes et al. 2007a, Krans 2011, Stopa 2011). Although pioneering and influential work (by,
for example, Lang 1977; for a recent review, see Ji et al. 2015) has perhaps led to an emphasis
on anxiety-related disorders, it is now timely to bring depression into focus. The idea of neg-
ative, intrusive image-based memories as seen in PTSD—that is, problematic autobiographical
memories—has relatively recently been extended to depression (e.g., Birrer et al. 2007), as noted
in recent reviews (e.g., Brewin et al. 2010, Holmes & Mathews 2010, Weßlau & Steil 2014).
What Does Dysfunctional Mental Imagery Look Like in Depression?
Depression is characterized by a range of mental imagery dysfunctions. Being aware of these dys-
functions may not only inform research into treatment development and mechanisms but also
guide clinical assessment, because many patients will not report mental images or their charac-
teristics unless explicitly asked about them (e.g., Beck et al. 1979, Bell et al. 2015, Hales et al.
2014).
Excess of intrusive negative imagery. At least two types of intrusive negative imagery have
been described in depression: imagery of past negative events, and suicidal imagery of the future.
Pioneering studies indicated the presence of intrusive negative memories of childhood trauma dur-
ing depressive episodes, with higher levels of intrusions associated with more severe depression
(Kuyken & Brewin 1994) (see Figure 1). Depressed individuals show higher levels of emotional
distress and avoidance of negative intrusive memories when compared to never-depressed individ-
uals, despite similar levels of self-reported intrusive memory frequency (Newby & Moulds 2011a).
Importantly, greater avoidance of such memories is associated with more OGMs in response to
positive and negative cues (Kuyken & Brewin 1995) (see Overgeneral Memory section below).
Interestingly, although intrusive memories are more common in PTSD than in depression, their
www.annualreviews.org Mental Imagery in Depression 253
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Figure 1
Negative intrusive imagery in depression. Many people with depression experience negative intrusive images, that is, distressing images
of memories or imagined events that intrude into awareness involuntarily. These could include, for example, intrusive images of
rejection, social isolation, or interpersonal conflict, and are often accompanied by intense negative emotions such as sadness, anxiety,
and guilt. Traditionally, CBT for depression has focused on negative verbal thoughts; negative images may also be a useful target for
treatment. Photograph reproduced by kind permission of Newscast Archives.
features are similar in each disorder—for example, in terms of vividness and the range of emo-
tions they may evoke, such as sadness, fear, anger, and guilt (Reynolds & Brewin 1999). Patel
and colleagues (2007) found that almost half of a depressed sample reported frequent distressing
intrusive images of memories or imagined events. Clinical examples of negative intrusive imagery
in depression include scenes of past childhood physical or sexual assault and images of humiliation
(e.g., being bullied at school), failure (e.g., being sacked from work), and overwhelming sadness
(e.g., losing a loved one).
Future-oriented intrusive mental images of suicide, also known as flash-forwards, have been
reported in depression and are associated with suicidal ideation (Holmes et al. 2007b). For example,
an inpatient with depression described her flash-forwards as seeing herself on a platform, and then
throwing herself in front of a train, which brought about a sense of calm at the time of despair,
254 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Figure 2
Lack of positive imagery in depression. Mental imagery allows most people to simulate and pre-experience possible future events,
whereas depressed individuals often struggle to imagine positive events happening in their future. Specifically, the images they generate
are less vivid than those generated by people who are not depressed. Photograph reproduced by kind permission of Newscast Archives.
allowing her to simulate whether she was prepared to complete the action (see also Crane et al.
2012, Hales et al. 2011). Relatedly, daydreaming with violent, imagery-based content has been
associated with emotional dysregulation in suicidality (Selby et al. 2007). We note that, far from
being seen as “positive,” the feeling of calm/relief associated with such suicidal imagery would be
of clinical concern in cases where suicidal acts are formulated as an escape from current difficulties.
Impoverished positive imagery. We suggest that depression is characterized not only by an
excess of negative imagery but also by impoverished positive imagery (see Figure 2). This impov-
erishment is reflected in the qualities of the positive mental imagery experienced and in difficulties
in using emotionally rich imagery-based processing to experience positive affect.
Reduced vividness. Initial evidence suggests that when people are depressed, they may find it
hard to generate vivid future- or past-oriented positive mental images. Future-oriented imagery
has been assessed using the Prospective Imagery Test (PIT; St ¨
ober 2000), in which participants
generate mental images from brief descriptions of hypothetical positive and negative future events
(e.g., “You will achieve the things you set out to do”) and rate their characteristics (e.g., vivid-
ness). Using the PIT, St ¨
ober (2000) found that participants with higher scores on questionnaire-
measured depressive symptoms scored lower on a combined imagery metric comprising speed,
vividness, and level of detail for positive, but not negative, future events. Similarly, reduced im-
agery vividness for positive, but not negative, future events has been found for dysphoric compared
www.annualreviews.org Mental Imagery in Depression 255
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
to nondysphoric participants (Holmes et al. 2008b) and for depressed participants compared to
healthy controls (Morina et al. 2011). Anderson & Evans (2015) similarly found that dysphoric
participants reported reduced vividness for images of positive self-generated future events com-
pared to nondysphoric participants. Sz˝
oll ˝
osi et al. (2015), using an unselected sample, found that
participants with higher questionnaire-rated depressive symptoms reported less vivid positive fu-
ture images but more vivid negative future images in response to single-word cues. Given the
function of mental imagery in simulating future events, selectively impoverished positive (relative
to negative) mental imagery could significantly limit the ability to imagine a positive future.
In relation to past-oriented imagery, Werner-Seidler & Moulds (2011) found that positive
memories recalled in response to word cues following a sad mood induction by formerly depressed
(i.e., currently euthymic) individuals were less vivid than those of never-depressed controls. In
contrast, negative memories were equally vivid across groups. However, when asked to recall
positive self-defining memories, i.e., memories of highly significant personal events, formerly
depressed participants rated their memories as equally vivid to those of never-depressed controls
(Werner-Seidler & Moulds 2012a), suggesting that vividness may be preserved for certain kinds
of memories. In the context of dysphoria, Anderson & Evans (2015) found no difference in the
vividness of memories for positive past events between dysphoric and nondysphoric participants.
Other studies using different methodology and types of imagery report no difference in positive
imagery vividness between dysphoric and nondysphoric (Benvenuti et al. 2015) or depressed and
nondepressed (Patron et al. 2015) groups. These studies used extended imagery tasks, in which
participants listened to a detailed script containing information about emotional and physiological
states, and had 90 seconds to create an image. This suggests that depressed individuals may be
able to generate vivid positive imagery if given appropriate scaffolding (cf. guided imagery, e.g.,
Lang 1979) but perhaps not in response to brief written cues. It is also worth noting that the
studies above have focused exclusively on the characteristics of deliberately generated imagery,
and investigation of differences in the characteristics of deliberately generated versus involuntary
spontaneous positive mental imagery is required.
Mood deterioration in response to positive information. Thinking about something positive
does not necessarily make you feel better. In fact, certain ways of thinking about positive informa-
tion can make you feel worse, and such thinking styles may predominate in depression. Joormann
et al. (2007) investigated the effect of recalling positive memories on mood in never-depressed,
formerly depressed, and currently depressed participants. Mood improved in never-depressed
participants, did not change in formerly depressed participants, and in fact worsened in currently
depressed participants.
The authors suggested that one possible mechanism for the worsening of mood in response
to positive information for depressed participants was the use of a ruminative, verbal, compara-
tive processing style (e.g., thinking “I used to be happy back then, now I just feel awful all the
time...”) rather than vividly reexperiencing a past positive event via imagery. Consistent with
this, experimental studies have found that using concrete or imagery-focused processing when
retrieving a positive memory leads to greater improvement in mood than does an abstract, verbal
style (Nelis et al. 2015, Werner-Seidler & Moulds 2012b). Similarly, instructions encouraging
verbal processing of positive hypothetical scenarios can result in no improvement in, or even a
worsening of, mood (e.g., Holmes et al. 2006, 2009b). Torkan et al. (2014) found that in the
absence of instructions to use any specific processing mode (e.g., imagery), depressed outpatients
experienced no improvement in depressive symptoms over the course of one week in which they
listened to descriptions of several hundred positive scenarios. Debriefing suggested that these par-
ticipants had tended to use a verbal, comparative processing style. However, whether depression
256 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
is in fact associated with individual differences in the tendency to use an imagery (e.g., as opposed
to a verbal) processing style, and in particular whether this may be different for positive versus
negative information, needs to be examined.
Observer perspective. Imagery perspective, or vantage point, has been investigated in depres-
sion. An event can be imagined from a field, or first-person, perspective or from an observer,
or third-person, perspective (Nigro & Neisser 1983). The former refers to the experiencing of
an event as if seeing it through one’s own eyes; the latter perspective refers to the position of an
onlooker or bystander, seeing oneself “from the outside” or as a “fly on the wall” (Nigro & Neisser
1983, pp. 467–468). Observer-perspective imagery, at least in the case of autobiographical mem-
ory, has been associated with reduced emotional impact compared to field-perspective imagery,
both in the context of PTSD (e.g., McIsaac & Eich 2002, 2004) and nonclinical studies (Nigro &
Neisser 1983).
A growing body of evidence from observational studies indicates that depression is associated
with a tendency to recall memories from an observer perspective and that this may be associated
with lower levels of affective content (e.g., Kuyken & Howell 2006; Kuyken & Moulds 2009;
Williams & Moulds 2007, 2008). This has mostly been investigated with regard to negative mem-
ories, for which it has been argued that the observer perspective is a form of cognitive avoidance
(Williams & Moulds 2007). However, this bias for observer perspective may also extend to positive
imagery, which could reduce its positive emotional impact. Lemogne et al. (2006) found that de-
pressed individuals are more likely to recall positive memories from an observer perspective than
are never-depressed controls. The same pattern has been observed in formerly depressed individ-
uals (Bergouignan et al. 2008), although not consistently (Werner-Seidler & Moulds 2011). In a
student sample, dysphoric individuals were more likely to use an observer perspective for positive
memories compared with negative memories, whereas nondysphoric students did not show this
differential pattern (Nelis et al. 2013).
Experimental evidence for the impact of perspective on the emotional impact of imagery is more
mixed: Holmes et al. (2008a) found that using a field perspective when imagining positive scenarios
resulted in a greater increase in positive affect than using an observer perspective, but Nelis et al.
(2012) did not find such an effect. Studies manipulating imagery perspective for negative intrusive
imagery (Williams & Moulds 2008) or positive memories and future projections (Vella & Moulds
2013) have found that shifting from field perspective to observer perspective reduces vividness
and associated emotion, but shifting from observer to field perspective does not consistently lead
to increases in such characteristics.
Slow to generate mental imagery. Although the above sections focus on the experience of
emotionally valenced mental imagery, some evidence suggests that depression is associated with
more basic problems in mental imagery generation and manipulation. Cocude et al. (1997) found
that depressed participants were slower than nondepressed control participants to generate images
in response to cue words (emotionally neutral nouns) and were sometimes unable to generate an
image at all. Chen et al. (2013b) found that people with MDD showed slower mental rotation (of
images of hands and letters) relative to healthy controls, and Chen et al. (2013a) further found
that slower mental rotation was positively related to the number of depressive episodes. However,
because nonimagery control tasks were absent in these studies, results may not apply specifically
to mental imagery generation and manipulation but instead may reflect generalized cognitive
slowing in depression (see, e.g., Zarrinpar et al. 2006). Additionally, the studies have examined
only neutral (as opposed to emotional) imagery. Nevertheless, if depressed individuals are slower
to generate and manipulate mental images, this may have implications for understanding mental
www.annualreviews.org Mental Imagery in Depression 257
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
imagery in depression and using it in treatment. For example, patients with depression might need
more guidance in generating imagery, and this could be useful to consider in therapy.
Overgeneral memory. OGM has been extensively studied in depression. Although the term
suggests that it pertains to a memory deficit rather than an imagery problem, the memory problem
or deficit is in essence also about difficulty generating specific mental imagery (Raes et al. 2006,
Sumner et al. 2014, Williams et al. 2007). A quote from the basic memory literature states: “When
people remember, they imagine, and when they imagine, they use memory” (Conway & Loveday
2015, p. 574). Conway & Pleydell-Pearce (2000) conclude that many scholars have rightly ascribed
a central role for imagery or image-based processes in remembering (specific) autobiographical
events (see also Rasmussen & Berntsen 2014). We first explain what OGM is and its (intrinsic)
link with imagery (dysfunction). Next, we discuss why it is likely not a trivial aspect of cognition
in depression.
OGM refers to a difficulty in voluntarily retrieving specific autobiographical memories. OGM,
or the specificity of one’s retrieval style, is typically assessed using a cue-word task, known as the
Autobiographical Memory Test (AMT; Williams & Broadbent 1986). The AMT consists of
positive and negative (sometimes also neutral) cue words (e.g., happy, disappointed). In response
to each cue, respondents are instructed to retrieve a specific memory, defined as a particular event
that occurred at a particular place and time and that lasted for less than one day. An example
of a specific memory retrieved in response to the cue word “happy” would be: “Last month, my
partner turned 38, and we celebrated the occasion with a day trip to Blankenberge at the Belgian
sea coast with our family.”
The link between memory specificity and imagery has been demonstrated in experimental
studies. In comparison with high-imageable cues, low-imageable cues typically lead to less specific
memories being recalled in the AMT (Anderson et al. 2012, Eardley & Pring 2006, Hauer et al.
2008, Rasmussen & Berntsen 2014, Williams et al. 1999). Reciprocally, an experimentally induced
specific retrieval style increases the ability to imagine (more detailed) future events compared to
induction of a more general retrieval style (e.g., Madore et al. 2014, Williams et al. 1996). Further,
neuroimaging studies indicate that remembering memories and imagining possible future events
show marked overlap in brain activity (e.g., Addis et al. 2007; for reviews and extended discussion,
see Schacter & Addis 2007, Schacter et al. 2012, Stawarczyk & D’Argembeau 2015) and that
specific memory recall relies on imagery-related processes and brain areas (e.g., medial parietal
regions; for a review, see Hach et al. 2014). In summary, imagery (in particular, but not exclusively,
visual imagery) appears to facilitate the retrieval of specific memories, and a specific retrieval style
in turn promotes imagery-based representations.
A large body of studies using the AMT over the past three decades has demonstrated that
depressed patients tend to retrieve less specific memories and/or more OGMs compared with
nondepressed controls (for a review, see Williams et al. 2007; for a recent replication of the basic
phenomenon, see Haque et al. 2014). Examples of such overgeneral (or “categoric”) memories
would be “going out with the family or friends” (in response to “happy”). OGM is not just a trivial
symptom or concomitant of depression but is clinically relevant as indicated, for example, by the
following empirical observations. OGM is negatively associated with problem-solving skills: A
less specific (or more overgeneral) retrieval style is associated with ineffective problem solving
of (hypothetical) interpersonal problems (e.g., Raes et al. 2005). This may be one mechanism by
which OGM contributes to depression. This correlational evidence (e.g., Raes et al. 2005) is also
supported by experimental work showing that the induction of a specific (versus general) memory
retrieval style leads to better problem-solving skills (e.g., Madore & Schacter 2015, Williams et al.
2006). Another finding that highlights the potential clinical importance of OGM is that it often
258 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
remains present in patients regardless of recovery or remission (e.g., Spinhoven et al. 2006; but see
Williams et al. 2005 for a nonreplication). This suggests that OGM is indeed not just a symptom
of depression but could be a vulnerability marker that remains present in asymptomatic periods.
Furthermore, prospective studies have shown that OGM has predictive value, in that higher levels
of OGM predict higher prospective levels of self-reported depression (see section below titled Do
Imagery Dysfunctions Play a Role in the Onset or Maintenance of Depression?).
Mental imagery in depressed phases of bipolar disorder. Scott et al. (2000) have shown
that individuals with bipolar disorder also exhibit OGM when depressed, a finding replicated by
Mansell & Lam (2004). Further, in bipolar disorder, as in unipolar depression, periods of suicidality
appear to be associated with the presence of intrusive flash-forward imagery of events related to
suicide (e.g., jumping off a cliff) (Hales et al. 2011). Suicidal imagery was rated as more vivid and
compelling in a group of patients with bipolar disorder than in those with unipolar depression
(Hales et al. 2011). Positive imagery is also rated as more vivid in individuals with bipolar disorder
compared to those with unipolar depression (Ivins et al. 2014), though this would likely typically
be associated with the euthymic or manic rather than the depressed phase of the disorder.
Comorbidity of depression in other disorders and related mental imagery. The kinds of
dysfunctional mental imagery described above may also be present when depression is comorbid
with another disorder or physical illness. For example, more severe depression has been found
among pain suffers who report experiencing mental imagery (Gosden et al. 2014). Among patients
with cancer, those with depression have been found to experience higher prevalence of negative
intrusive images, with these linked to maladaptive coping (Brewin et al. 1998). Where disorders
overlap with depression in terms of symptoms (e.g., depressed mood), there may also be overlap
in related mental imagery phenomena. For example, reduced specificity for both autobiographical
memory and future events has been associated with PTSD (Kleim et al. 2014a) and complicated
grief (Maccallum & Bryant 2011, Robinaugh & McNally 2013), in particular for imagined future
events including the deceased (Robinaugh & McNally 2013). These comorbidities and overlaps of
mental imagery phenomena highlight the importance of assessing mental imagery where depressed
mood may be a problem, regardless of whether this is the primary complaint.
Mental imagery and biased information-processing accounts. Many cognitive processes have
been implicated in depression (Beck & Haigh 2014, Gotlib & Joormann 2010), and imagery needs
to be considered within this scope. The mental imagery phenomena described above do not occur
in isolation but rather in the context of other negative biases in, for example, attention, memory,
and interpretation. These processes may interact with and exacerbate each other (Everaert et al.
2012, Hirsch et al. 2006, Holmes et al. 2009a). For example, when thinking about an upcoming
event, not only may a depressed individual be less likely to think of positive possibilities, but if they
do, these possibilities will be less vivid, or dimmer in their mind’s eye, reducing their believability
or motivational power (cf. D’Argembeau & Van der Linden 2012, Szpunar & Schacter 2013).
Mental imagery may therefore exacerbate and amplify other maladaptive processes in depression
(Holmes et al. 2009a).
Do Imagery Dysfunctions Play a Role in the Onset or Maintenance
of Depression?
The previous sections reviewed evidence for differences in the experience of mental imagery in
depressed individuals relative to healthy controls. In this section, we consider whether mental
www.annualreviews.org Mental Imagery in Depression 259
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
imagery may prospectively account for changes in depression symptoms over time. Our focus is
on evidence pertaining to intrusive imagery, lack of positive imagery, and OGM.
Limited evidence suggests that intrusive memories may predict future depression. Brewin
et al. (1999) found that the frequency of intrusions of stressful memories predicted self-reported
depression scores at six-month follow-up in 62 depressed patients. In a community sample of 33
individuals who reported an intrusive memory at baseline, Newby & Moulds (2011b) found that
greater intrusiveness predicted higher levels of depression at a six-month follow-up.
Indirect evidence that positive imagery protects against depression comes from experimen-
tal studies showing that positive mental imagery promotes cognitive, emotional, and behavioral
responses that run counter to depression. Holmes et al. (2009b) found that, among healthy volun-
teers, engaging in positive imagery (compared to verbal processing of the same positive material)
led to a greater positive interpretive bias and increases in positive mood, and was protective against
a subsequent negative mood induction. Further, within a dysphoric sample, Pictet et al. (2011)
found that engaging in positive, as opposed to negative or mixed-valence, imagery led to a greater
positive interpretive bias, increased positive mood, and increased goal-directed behavior on a lab-
oratory task. Finally, Torkan et al. (2014) found that repeated imagery of positive scenarios (versus
just listening to the same scenarios) over one week resulted in decreased depressive symptoms and
reduced negative interpretive bias in participants with depression.
A prospective study in medical interns found that a bias to generate positive, rather than nega-
tive, mental images when imagining ambiguous scenarios (but not imagery vividness) was predic-
tive of lower levels of future depressive symptoms over six months (Kleim et al. 2014b). However,
this study does not differentiate this imagery-based bias from a general (i.e., unrelated to imagery)
negative interpretive bias. Further prospective studies are needed to examine whether imagery-
related interpretation biases specifically are predictive of future depression, and the prospective
role of imagery vividness remains to be explored. Future studies should investigate the unique
contribution of the representational format (i.e., imagery versus verbal) of impoverished positive
cognition (and intrusive negative cognitions) to the onset or maintenance of depression.
Several studies have investigated the potential role of OGM in the onset and maintenance of
depression. A meta-analysis of 15 studies concluded that OGM is a predictor of an unfavorable
course of depressive symptoms, particularly in those with clinical depression (Sumner et al. 2010).
More recent studies have generally confirmed that conclusion. For example, Van Daele et al. (2014)
showed that OGM was associated with a linear increase in self-reported depressive symptoms
over 18 months in a community sample. Other studies have qualified the general conclusion,
for example, by showing that OGM interacts with stress in predicting higher future levels of
depressive symptoms (Anderson et al. 2010). Results in younger age groups, however, are less
consistent, with some studies reporting a positive association between OGM and prospective
depressive symptoms in (high-risk) adolescents (e.g., Hipwell et al. 2011), whereas others have
not found such an association (e.g., Crane et al. 2016).
The value of OGM in predicting depressive diagnostic status has been examined far less thor-
oughly, and results are more mixed than is the case for OGM predicting prospective symp-
tom levels. Kleim & Ehlers (2008) found that OGM predicted greater likelihood of diagnosis of
MDD at 6-month follow-up in assault victims. Sumner et al. (2011) found that OGM predicted
depressive relapse over a 16-month follow-up period in adolescents in remission from MDD
or minor depressive disorder, albeit only among those participants experiencing high levels of
chronic interpersonal stress. Spinhoven et al. (2006), however, found no predictive association
between OGM in formerly depressed patients and recurrence of a major depressive episode over
a two-year follow-up. Finally, no study to date has tested whether OGM predicts first onset of
depression.
260 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Taking a Developmental Perspective on Mental Imagery in Depression
Developments during childhood and adolescence in cognitive abilities, emotional processing, and
social interactions are thought to impact mental health risk (Davey et al. 2008, Steinberg 2005).
Understanding how these processes relate to mental imagery phenomena relevant to depression
and their potential implications for treatment strategies is of interest for addressing depression
in individuals of different ages; it may also shed light on the etiology of depression symptoms.
Ultimately, it is only by taking a longitudinal, developmental perspective that we can begin to
disentangle causal and vulnerability risk factors from maintenance and compensatory strategies
and downstream effects of symptoms. Adolescence and young adulthood is arguably the major
period of life for the onset of mental health problems (Kessler et al. 1994, Ormel et al. 2014, Paus
et al. 2008). Vulnerability to adult psychological disorders is thought to be traceable to childhood
factors (Caspi et al. 1996, Gregory & Eley 2007, Rutter 1984). However, still, the majority of
mental health research is conducted with adults.
Developmental research has revealed a number of findings that are potentially relevant to un-
derstanding and using mental imagery across development (Burnett Heyes et al. 2013). Mental
imagery is a preferred mode of processing from early childhood (Harris 2000) and can be har-
nessed to aid performance in cognitive tasks ( Joh et al. 2011, Mischel et al. 1989). The continued
development throughout childhood and adolescence in aspects of cognitive control (Anderson
et al. 2001, Luna et al. 2004, Weil et al. 2013) may impact the degree to which individuals have
control of and/or insight into mental imagery. This may have implications for understanding the
lifetime increase in risk for depression during adolescence (Kessler et al. 1994, 2012). Emerging
cognitive abilities may make child and adolescent patients more vulnerable to intrusive, unhelpful
mental imagery. At the same time, greater cognitive flexibility, particularly in adolescence, could
mean that interventions delivered during this time will have lasting impact (Hauser et al. 2015,
Stevenson et al. 2014, van der Schaaf et al. 2011). More research is needed on the interplay be-
tween mental imagery, psychopathology, and cognitive abilities during development. In addition,
investigators need to examine whether individuals of different ages are differentially vulnerable
to distinct mental imagery phenomena and, conversely, whether they may benefit from distinct
mental imagery–based treatment strategies.
Does Adaptive Mental Imagery Contribute to Resilience?
The above sections have described ways in which various aspects of mental imagery have been
linked to depression. Taken together, the evidence reviewed in these sections implies that mental
imagery in depression differs from that associated with healthy functioning. A further, related
possibility is that certain kinds of mental imagery are in fact protective against depression and
contribute to resilience. Resilience, the ability to adapt well to or “bounce back” from adversity or
trauma (e.g., Southwick & Charney 2012), has been considered in terms of genetic, environmental,
and cognitive factors, among others. If any aspects of adaptive or helpful mental imagery contribute
to resilience, then these could potentially be targets for preventive interventions.
One factor associated with resilience that has been linked to mental imagery is optimism.
Optimism, the tendency to have a generalized positive expectation about the future, appears
to confer resilience to a variety of stressors (Carver & Scheier 2014, Carver et al. 2010) and
may be related to future-oriented mental imagery. Sharot et al. (2007) carried out a functional
magnetic resonance imaging (fMRI) study in which healthy volunteers generated future- and
past-oriented mental images in response to positive, negative, or neutral word cues. The more
optimistic participants were, the greater their sense of pre-experiencing and the closer in the future
www.annualreviews.org Mental Imagery in Depression 261
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
they imagined the positive relative to negative future-oriented images. In a community sample
of 237 adults, Blackwell et al. (2013) found that higher levels of optimism were associated with
more vivid positive future-oriented mental imagery (measured using the PIT). This relationship
remained significant when controlling for sociodemographic factors and everyday imagery use.
Although it is not possible to draw conclusions about causality from such correlational data,
together these results suggest that the extent to which people are optimistic about their future
relates to the qualities (such as vividness) of their future-oriented mental imagery.
Could positive mental imagery–based interventions be used to increase optimism and thus
resilience? Meevissen et al. (2011) asked healthy volunteers to practice a “best possible self” (BPS)
imagery exercise every day for two weeks. The BPS exercise involved imagining a future self in
which everything had turned out in the best possible way. Compared to a control condition (imag-
ining activities of the previous day), participants in the BPS imagery condition showed a significant
increase in self-reported optimism over the intervention. However, the precise mechanism for the
increase in optimism, for example, whether the BPS exercise led to increased vividness of positive
future imagery, is not clear. Future research should examine the mechanisms linking functional
mental imagery to optimism and whether inducing increases in optimism via mental imagery
confers benefits for resilience.
Other ways in which adaptive mental imagery could contribute to resilience are via its use
in emotion regulation. For example, positive affect has been linked to resilience (Fredrickson &
Joiner 2002), and mental imagery provides one way in which positive affect can be generated.
Mental imagery can also be used to self-soothe and generate a sense of safety; for example, an
image of a “perfect nurturer” can be created to help an individual generate a sense of safeness and
experience feelings of warmth and kindness toward themselves (Lee 2005; see also Gilbert 2009).
MODIFYING MENTAL IMAGERY IN DEPRESSION
Implications of Mental Imagery for Cognitive Behavioral Interventions
in Depression
In comparison to verbal cognition, imagery appears to have been relatively neglected in evidence-
based psychological treatments for depression, such as CBT. However, in practice, psychological
treatment techniques have long been associated with mental imagery, including Janet’s work on
imagery substitution in the late-nineteenth century and Jung’s work on active imagination in the
early-twentieth century (discussed in Edwards 2007). CBT has primarily considered imagery in
the context of anxiety (Beck et al. 1974), and thus techniques to specifically tackle negative intrusive
imagery in depression have only evolved more recently.
Excess of negative imagery. In their manual describing cognitive therapy for depression, Beck
et al. (1979) refer to both “thoughts and visual images” (p. 8) as cognitions of relevance and note
some specific uses and features of imagery relevant to the treatment of depression. For example,
they suggest that imagery of unpleasant and pleasant situations can be used to highlight the
influence of cognitions on mood, that imagery of pleasant scenes can be used to alleviate dysphoria,
and that imaginal rehearsal can be used as “stress inoculation” against future crises. Discussing
anxiety-inducing images, Beck et al. (1979) note that patients might not report mental imagery
unless the therapist specifically inquires about it (as previously noted), but that once elicited,
images can be controlled by changing the visual content (similar to imagery rescripting, discussed
below). Research into methods to modify negative intrusive imagery in depression is more recent.
Techniques range from imaginal exposure to the problematic images (Kandris & Moulds 2008)
262 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
to transforming the content of the imagery via imagery rescripting (Brewin et al. 2009, Patel et al.
2007, Wheatley et al. 2007). Another approach could be to change maladaptive appraisals about
having intrusive imagery (Lang et al. 2009, Wells et al. 2009). Although promising, this work is at
an early stage and requires further treatment studies. It is of use, however, to consider the larger
literature on such techniques for intrusive imagery in other disorders, such as PTSD.
Mental imagery techniques also form part of schema therapy (ST), an integrative treatment
approach to chronic and lifelong problems combining cognitive-behavioral, interpersonal, expe-
riential, and psychodynamic techniques (Young et al. 2003). In ST, mental imagery is used to
explore maladaptive schemas in patients and to change the emotional experiences associated with
these schemas. For example, imagery of traumatic childhood experiences can be used in ST to
help the patient reexperience aspects of traumatic events in a safe setting, in order to thereby
decrease the emotional impact of the traumatic memory. Although ST has primarily been applied
to the treatment of personality disorders, more recently a schema therapy model for (chronic) de-
pression has been described (Renner et al. 2013). Initial evidence from single-case series suggests
that ST could be an effective treatment for chronic depression (Malogiannis et al. 2014, Renner
et al. 2015).
Impoverished positive imagery. Enhancing/boosting positive mental imagery may provide a
useful adjunctive approach for cognitive-behavioral approaches to depression, which have tended
to focus on negative information processing (e.g., Dunn 2012, MacLeod & Moore 2000). In partic-
ular, given the studies discussed previously, it could be useful to encourage vivid, field-perspective,
positive mental imagery and to promote imagery-based processing of positive information.
One possibility starting to be explored is the potential to enhance positive mental imagery
in depression via simple computerized cognitive training methods. Positive imagery cognitive
bias modification (CBM) involves repeated practice in generating positive mental imagery, in the
context of initially ambiguous training stimuli, to create a more positive imagery bias. For example,
in one version of the training, participants listen to brief descriptions of everyday situations that
are structured so that they are initially ambiguous but always resolve positively. Participants are
instructed to vividly imagine themselves in the scenarios as they unfold, as if actively involved
in the situations described, and thus they practice generation of vivid, field-perspective, positive
mental imagery. Imagery CBM was developed via experimental work with healthy volunteers (e.g.,
Holmes et al. 2009b), and clinical studies subsequently started to investigate its potential role as
a treatment tool in depressed individuals (Blackwell & Holmes 2010, Lang et al. 2012, Torkan
et al. 2014).
Focusing on a relatively neglected cognitive aspect of depression, positive mental imagery, al-
lows the possibility of treating additional targets that conventional treatments struggle to address.
Recent research (also discussed below) raises the possibility that imagery CBM may be useful in
tackling a specific aspect of depression that poses a challenge to current treatments and predicts
poor treatment response, namely anhedonia (Blackwell et al. 2015). Anhedonia, the loss of interest
in or enjoyment from activities, is one of the core symptoms of depression (Am. Psychiatr. Assoc.
2013), and its characterizations include a deficit in positive affectivity and both reduced anticipa-
tion and experience of pleasure (Pizzagalli 2014). The positive affect generated during imagery
CBM and repeated simulation of positive outcomes from everyday activities provides potential
mechanisms for reducing anhedonia.
As a computerized intervention, imagery CBM can be delivered remotely and/or in combi-
nation with other Internet-delivered treatments such as Internet-delivered CBT (Williams et al.
2013, 2015). However, research in imagery CBM as an intervention is at an early stage, and find-
ings are mixed. Despite promising findings in initial small-scale clinical studies testing a one-week
www.annualreviews.org Mental Imagery in Depression 263
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
intervention (Blackwell & Holmes 2010, Lang et al. 2012, Torkan et al. 2014), when scaled up
to a four-week intervention in a randomized controlled trial (RCT) with 150 currently depressed
participants, Blackwell et al. (2015) found that, overall, imagery CBM resulted in no greater reduc-
tion in symptoms of depression than a control sham CBM intervention. Furthermore, although
Blackwell et al. (2015) found greater reduction in anhedonic symptoms of depression over the
imagery compared to control intervention, this analysis was posthoc, and thus these findings need
replication. If successfully developed, imagery CBM could be used as an adjunct to treatments
that do not incorporate a positive imagery focus, such as conventional CBT for depression.
Training mental imagery as a mode of processing could also provide a route to enable depressed
individuals to experience an improvement in mood in response to positive information (see the
section above titled Mood Deterioration in Response to Positive Information). For example,
Werner-Seidler & Moulds (2012b) found that both currently and recovered depressed individuals
experienced an increase in positive mood after recalling a positive memory if they were instructed
to use a “concrete” processing mode that focused on generating rich mental imagery (as opposed
to an abstract, verbal processing mode). The exact parameters by which depressed individuals
can use positive memories to improve their mood need further investigation (Werner-Seidler &
Moulds 2014). Generating positive imagery may also have beneficial effects on implicit affective
processing (G ¨
orgen et al. 2015). One fruitful avenue for future treatment innovation might be
to focus on techniques for boosting physiological response during mental imagery, a method
developed by Peter Lang and colleagues for anxiety (Lang et al. 1980, Miller et al. 1987). Overall,
providing instructions and training in using mental imagery may increase the ability of individuals
with depression to carry out mood repair effectively.
Overgeneral memory. As reviewed above, accumulating evidence suggests that OGM plays an
important role in increased vulnerability to emotional disorders (depression and PTSD in particu-
lar). Therefore, reducing or remediating OGM is a compelling target for therapeutic intervention.
A first exploration into this potential translational treatment for depression was conducted by
Raes et al. (2009), who developed the group-based MEmory Specificity Training (MEST) pro-
gram to train specific retrieval of personal memories in order to counter OGM. MEST consists
of four weekly one-hour group sessions. The main component is repeated practice in recalling
specific memories in response to both neutral and emotional (positive and negative) cue words.
During practice, patients are encouraged to recall as much contextual and sensory-perceptual
detail as possible in the process of generating and describing specific memories. For each mem-
ory that is retrieved, patients are invited to generate a vivid and detailed image of their specific
memories and to imagine the event as vividly and clearly as possible. The program further in-
cludes psychoeducation (about memory problems in depression more generally) and homework
exercises (for more details, see Raes et al. 2009). In an uncontrolled pilot study of 10 depressed
inpatients, memory retrieval style indeed became significantly more specific over the four-week
intervention (Raes et al. 2009). Furthermore, the observed improvements in memory specificity
were significantly associated with improvements in problem-solving skills, cognitive avoidance,
and rumination, all variables that are hypothesized to mediate the impact of memory specificity on
the course of depression. A recent uncontrolled study found that MEST also resulted in increased
specificity of memory retrieval in 32 depressed outpatients (Eigenhuis et al. 2015).
The uncontrolled pilot of Raes et al. (2009) was followed by an RCT comparing five sessions
of MEST to a control condition (with no additional contact) in 23 depressed adolescents (Neshat-
Doost et al. 2012). Repeated practice in retrieving specific memories was again the main component
of the program. For the group receiving MEST, but not the control group, there was a significant
increase in memory specificity and a significant decrease in depressive symptoms at follow-up.
264 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Improvements in depressive symptoms in the MEST group were mediated by changes in memory
specificity.
The results of these pilot trials suggest that MEST indeed holds promise as a relatively simple
therapeutic intervention for depression. As a logical next step, MEST is currently being compared
to an active (education and support) control condition in a Phase II RCT in 60 depressed adults
(Dalgleish et al. 2014). From a basic science perspective, Schacter (2013) recently referred to
MEST as an illustration of how basic research findings may be usefully applied or translated to
daily life in general or to clinical practice more specifically. The ongoing Phase II trial and other
future studies will determine whether MEST can live up to its promise as an effective depression
intervention.
A recently developed intervention that also aims to ameliorate depression via intensively train-
ing individuals to become more specific in their thinking is concreteness training (CNT; Watkins
et al. 2009). Whereas MEST is mainly a clinical translation of theoretical and experimental work
on OGM, CNT explicitly builds on the wider literature on overgeneralized thinking (including
OGM) and rumination in depression, where rumination is conceptualized as an abstract (antithet-
ical to a more helpful concrete) thinking style.
Participants undergoing CNT work with standardized events (scenarios) in addition to personal
events (specific autobiographical memories) and are trained to process those events in a concrete
fashion (using mental imagery, focusing on sensory details and promoting so-called how thinking
as opposed to abstract-ruminative why thinking). Following initial proof-of-principle studies in
dysphoric individuals (Watkins & Moberly 2009, Watkins et al. 2009), Watkins et al. (2012)
conducted a Phase II RCT in which clinically depressed individuals were randomized to treatment
as usual (TAU), TAU +CNT, or TAU +relaxation training (RT). TAU +CNT resulted in
greater increases in concreteness and greater decreases in rumination and overgeneralization in
comparison with both control groups. TAU +CNT resulted in significantly greater decreases
in self-reported depressive symptoms in comparison with TAU but not with TAU +RT.
To test whether CNT exerts a beneficial effect on depressive symptoms through an improve-
ment in the hypothesized mechanism of concrete processing or alternatively via nonspecific fac-
tors, Mogoas¸e et al. (2013) focused on CNT’s essential component, that is, concrete processing
training, in the absence of a therapeutic context (no contact with a trainer, and not presented as
a depression intervention). This “pure” CNT was delivered for seven consecutive days via the
Internet to dysphoric students (N=42), and its effects were compared to a no-intervention con-
trol. The process differed from previous CNT studies in that participants practiced using only
standardized scenarios and not personal autobiographical memories. Autobiographical memory
specificity was assessed using the AMT. Results showed that, as in the previous studies (Watkins
et al. 2009, 2012), the students who received CNT had significantly greater increases in concrete-
ness than did the control group, but the increases did not lead to greater memory specificity or to a
reduction in depressive symptoms or rumination. As such, questions regarding the key therapeutic
ingredient of CNT remain outstanding.
Both MEST and CNT can be regarded as forms of CBM interventions. The bias in this case
is OGM recall, or more broadly, overgeneralized (abstract) thinking. The work conducted so
far with MEST and CNT suggests that these are promising interventions. Yet, we agree with
Cristea et al. (2015, p. 15) that what is sorely needed are sufficiently powered randomized trials
in clinical participants, using adequate (e.g., common factors) control groups, and conducted by
independent research groups. Meanwhile, we also note that where further development is needed
in CBM (and contrary to Cristea and colleagues’ conclusions), we believe small experimental stud-
ies will be valuable in science-driven treatment innovation and for understanding the underlying
mechanisms, such as imagery.
www.annualreviews.org Mental Imagery in Depression 265
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Other memory and imagery-related approaches. The broader literature on mental imagery
suggests additional ways in which mental imagery could be used to enhance cognitive-behavioral
interventions for depression (Holmes & Mathews 2010). For example, the method-of-loci strategy,
in which mental imagery is used to associate to-be-remembered information with locations along a
familiar route, has been suggested as a means to facilitate recall of positive memories in depression
(e.g., Dalgleish et al. 2013, Dalgleish & Werner-Seidler 2014).
Mental imagery could also potentially be of benefit in behavioral activation (BA) interventions
for depression. Different forms of BA interventions for depression have been proposed, but the
basic assumption is that depression occurs when a person engages in avoidance behavior and en-
gages less frequently in pleasant, potentially rewarding activities (Martell et al. 2010). The aim of
BA interventions is to increase engagement in reinforcing activities through activity scheduling,
thereby enabling the person to experience reward and positive reinforcement. What role can men-
tal imagery play in BA for depression? Mental imagery allows us to simulate possible (rewarding)
events in the future. It has been shown that mental imagery of future behaviors increases the
chances of actually acting out this behavior.
Loft & Cameron (2013) found that participants who engaged in a two-minute imagery exercise
twice each day for 21 days involving visualizing the steps to prepare for quality sleep experienced
improvements in sleep behaviors, sleep quality, and time to sleep when compared with participants
in an active control condition (arousal reduction) and participants in a neutral imagery control
condition. Similar imagery exercises have also been shown to increase motivation for physical ex-
ercises (Duncan et al. 2012) and to promote engagement in physical activities (Chan & Cameron
2012). Such imagery instructions could perhaps also be used in combination with BA principles
to help individuals with depression engage in rewarding and reinforcing activities. Although this
hypothesis has not been tested so far, it has been shown that dysphoric individuals who were
instructed to generate positive images in response to picture-word cues experienced more posi-
tive affect and performed better on a subsequent behavioral laboratory task when compared with
participants who were instructed to generate negative images or participants in a mixed valence
(control) condition (Pictet et al. 2011). Studies unrelated to psychopathology have also used im-
agery to increase behavior, for example, to increase consumption of healthy fruit (Kn¨
auper et al.
2011). Together, these studies suggest that mental imagery can have a behavior-enhancing effect,
which when combined with BA principles could potentially tackle depression through increased
reward and positive reinforcement experiences. However, further research is needed.
MECHANISMS OF MENTAL IMAGERY IN DEPRESSION
Can Investigating Mental Imagery Help Us Better Understand the Mechanisms
Underlying Depression?
What do we mean by the term mechanism? Mechanisms of psychological change, for exam-
ple, those brought about by treatment, are defined as “The basis for the effect, i.e., the processes
or events that are responsible for the change; the reasons why change occurred or how change
came about” (Kazdin 2007, p. 3). More broadly, an understanding of mechanisms provides the
essential causal link in revealing how processes interact to yield phenomena of interest (Bechtel
2009). Mechanisms underlie causal inference and causal explanation and are an important consid-
eration in any attempt to modify observed phenomena. In addition to treatment (or, conversely,
maintenance) mechanisms, etiological or “risk” mechanisms are also defined (Kraemer et al.
1997). Typically, psychological treatments target mechanisms hypothesized to be involved in the
266 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
maintenance of clinical symptoms, whereas basic science disciplines often seek to understand
mechanisms of etiology or risk. It is clear that we do not fully understand mechanisms of mental
imagery in depression risk, maintenance, or treatment. Ultimately, we need to consider mecha-
nisms at all levels of explanation—behavioral, cognitive, emotional, neural, and molecular; their
interrelations; and their interactions with the environment (Morton & Frith 1995) (see Figure 3).
The US National Institute of Mental Health has called for a focus on mechanisms in clinical
research identifying disease and treatment targets, noting, “The term ‘target’ refers to a hypoth-
esized mechanism of action and its ability to modify disease, behavior, or functional outcomes”
(Natl. Inst. Ment. Health 2014). Targets can range from molecular- and circuit-level mechanisms
proposed for pharmacologic agents, to neural systems and cognitive processes for psychosocial
behaviors, to the decision-making or organizational behaviors of a service providing an interven-
tion (Natl. Inst. Ment. Health 2014). One example of studying mechanisms at a particular level
of explanation is to consider the cognitive neuroscience of mental imagery in depression.
How might investigating mental imagery and neural mechanisms help? Can understanding
neural mechanisms advance our understanding of depression and promote treatment innovation?
Recently, it has been argued that for future mental health treatment innovation, neuroscience
findings should be better integrated into mainstream clinical research (Holmes et al. 2014, Roiser
2015).
A wealth of neuroscientific evidence suggests that memory, imagery, and perception draw on
both shared and distinct neural components (Kosslyn et al. 2006). For example, episodic mental
imagery of past and future events recruits medial temporal lobe structures that are involved in
autobiographical memory, such as the hippocampus, with fMRI activity levels in healthy controls
correlated with imagery vividness and detail (Addis & Schacter 2008). A recent meta-analysis con-
cluded that brain structures in the default network, specifically the medial prefrontal cortex, are
involved in both personal episodic future imagery and spontaneous mind-wandering (Stawarczyk
& D’Argembeau 2015). In a study comparing depressed and nondepressed participants, past and
future episodic imagery was generated during fMRI in response to cue words referring to com-
monly experienced events (Hach et al. 2014). During the relatively smaller number of trials for
which depressed participants were able to recall a detailed, specific autobiographical memory,
participants showed underrecruitment of brain regions supporting memory specificity (e.g., hip-
pocampus). Nevertheless, the same basic brain regions were recruited by both groups of partici-
pants. This finding could be leveraged to shed light on how, why, and for whom imagery-based
treatments work. For example, does imagery training enhance the ability and tendency to generate
imagery, and are these changes associated with normalized neural activity in the critical episodic
imagery network? Can investigation of differences in neural response to autobiographical mem-
ory generation be used to develop methods for identifying treatment responders (cf. Roiser et al.
2012)?
Cognitive neuroscience findings could potentially be used to optimize treatment for individual
patients via neurofeedback. In this procedure, neuroimaging data are relayed to participants in
real time for use as a training signal to regulate brain activity. Conceptually, this is analogous to
giving participants detailed verbal feedback on a trial-by-trial basis during a cognitive interven-
tion. In one study, depressed participants used fMRI neurofeedback to regulate activity in brain
regions responsive to emotionally positive (versus neutral) visual stimuli, including the anterior
insula, hippocampus, and a number of prefrontal regions (Linden et al. 2012). During debriefing,
participants reported that they had gradually learned to adopt a positive mental imagery strategy
to regulate brain activity, with beneficial impact on mood and clinical symptoms. Clearly, these are
www.annualreviews.org Mental Imagery in Depression 267
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
MEST
BIOLOGY
BEHAVIOR
COGNITION
ENVIRONMENT
Treatment
mechanisms:
BIOLOGY
Maintenance
mechanisms:
BIOLOGY
Maintenance
mechanisms:
COGNITION
Maintenance
mechanisms:
ENVIRONMENT
Maintenance
mechanisms:
BEHAVIOR
Treatment
mechanisms:
BEHAVIOR
Poor
problem
solving
Behavioral
withdrawal
Excess
negative/
lack of
positive
imagery;
OGM
What is the
neural basis
of imagery
dysfunction?
Social
isolation
Hippocampal
activity
Treatment
mechanisms:
COGNITION
Treatment/risk
mechanisms:
ENVIRONMENT
Eects
of trauma
Targeting
OGM;
e.g. MEST
Cut out and fold
Figure 3
A “chatterbox” origami model to show in 3D the mechanisms of depression at behavioral, cognitive, biological, and environmental
levels of explanation. The figure can be cut out and assembled along the dotted lines (search “how to make a chatterbox” online for
instructions). The entire model represents an individual with depression. Move apart the four apices to reveal examples of either
maintenance (blue) or treatment target (brown) observations and hypothesized mechanisms. Behavioral observations constitute directly
observed experimental and clinical variables; for example, fewer specific details recalled during an autobiographical memory task or
clinical observations of reduced spontaneous activity. At the cognitive level are the mental processes hypothesized to result in these
behavioral observations; these are unobservable directly but must be inferred on the basis of controlled experiments. At the biological
level are molecular or systems neuroscience mechanisms thought to underlie cognitive and behavioral phenomena. Finally, at the
environmental level are environmental risk factors and factors thought to exert a broad impact on an individual. All levels are relevant for
understanding depression in an individual person. Abbreviations: MEST, MEmory Specificity Training; OGM, overgeneral memory.
268 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
early days, but such studies illustrate the potential for cross talk between cognitive neuroscience
and clinical psychopathology research.
Moving mechanisms forward: bridging cognitive science, mental imagery, and emotion.
In order to more fully understand the neural mechanisms of mental imagery in depression, a
more fine-grained approach at the cognitive level of explanation is needed. Over several decades,
research led by Kosslyn has delineated a set of tools for investigating the cognitive operations re-
cruited during mental imagery tasks. Four key components are identified (Kosslyn 1996, Kosslyn
et al. 2006): (a) image generation, or the formation of an image in the “mind’s eye”; (b)image
inspection, or the shifting of attention to a particular aspect of an image; (c) image maintenance, or
the retention of an image; and (d) image transformation, for example, mentally rotating imagined
objects (for the relation of these concepts to clinical psychology, see Pearson et al. 2013). Each of
these four processes may be recruited to a greater or lesser extent in a given mental imagery task,
and each can in turn be subdivided into more basic, domain-general cognitive components, such
as autobiographical memory retrieval, working memory maintenance, and attentional selection
(Kosslyn et al. 1984, 2006). This basic cognitive science framework highlights cognitive subcom-
ponents of mental imagery, which is a useful basis for designing well-controlled experimental
tasks. However, there is still a gulf between this fundamental research and imagery of meaningful
and emotion-laden events, and more research that speaks directly to the links between mental
imagery, emotion, and clinical symptoms is required.
Experimental work has demonstrated that compared to verbal processing, imagery has a more
powerful impact on emotion (Holmes & Mathews 2005; Holmes et al. 2006, 2008c; Nelis et al.
2012). The impact on emotion is not just for fear, but for emotions also highly relevant in
depression—positive and negative affect. Holmes & Mathews (2010) have suggested that the
impact of imagery on emotion is brought about in several ways, such as by the similarity be-
tween imagery and actual perception and by imagery’s close link to autobiographical memory (see
Figure 4). We suggest that it will be important to better illuminate the mechanisms underlying
mental imagery and emotion both to ameliorate negative affect in depression and to boost positive
affect.
CONCLUSIONS
This review highlights the potential importance of mental imagery in depression as well as the
fact that this research is at a very early stage. Exciting gaps persist in our understanding of the
potential role of mental imagery in the etiology, maintenance, and treatment of depression, and
outstanding questions for future research remain, as we have highlighted throughout. A focus on
mechanisms (Craske 2014, Holmes et al. 2014), in relation to both dysfunctional imagery and
psychological techniques to target it, may be particularly useful. Such a focus could enable better
links to be made between different levels of explanation, such as those addressing forms of imagery
and memory at a neural level (e.g., Clark et al. 2014, 2016; Hach et al. 2014; Ramirez et al. 2015)
(see Figure 3). It could also facilitate links between a psychopathology lens (e.g., specific imagery
dysfunctions such as difficulty generating positive future-oriented images) and an understanding of
the importance that adaptive imagery may play in our everyday lives (such as in mental simulation
and anticipation of actions).
In this review, we have suggested that people with depression may suffer from an excess of
intrusive involuntary negative mental imagery yet also experience impoverished positive imagery,
and further may have difficulty voluntarily generating specific images of the past or future. Focusing
on mental imagery in depression provides the opportunity to understand an important yet relatively
www.annualreviews.org Mental Imagery in Depression 269
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Top-down
control processes
Bottom-up
sensory cue
Associates:
action readiness, believability,
attitude to self, etc.
Processing overlaps
with perceived events
Autobiographic and
semantic memory
knowledge base
Little overlap with
processing of perceived events
Direct contact with
emotional systems
Contact with other
semantic knowledge
Constructed/reconstructed
image of emotional instance
Verbal representation
of emotional meaning
SELECT FROM
MATCHING
Figure 4
Bridging cognitive science, mental imagery, and emotion: the construction of imagery versus verbal representations, and their relative
impact on emotion. See also (Holmes & Mathews 2010).
neglected aspect of cognition that has a powerful emotional impact and numerous roles in our
everyday life. This adds color to our understanding of underlying mechanisms in depression
and may help develop more effective and adjunctive treatment techniques for this common and
disabling disorder.
SUMMARY POINTS
1. Dysfunctional mental imagery plays a potentially important role in depression, but re-
search is at an early stage.
2. Imagery dysfunctions in depression include an excess of intrusive mental imagery, im-
poverished positive imagery, observer perspective imagery, and overgeneral memory (in
which specific imagery is lacking).
3. Emerging evidence indicates that intrusive negative imagery and overgeneral memory
may prospectively account for changes in depression symptoms over time.
4. Imagery dysfunctions in depression may add a useful target for treatments, including
psychological interventions, such as forms of cognitive behavioral therapy or memory
specificity training, and emerging cognitive training paradigms.
270 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
FUTURE ISSUES
1. Future studies are needed to advance our knowledge of mechanisms underlying mental
imagery and emotion in depression, both to ameliorate negative affect and to boost
positive affect.
2. The contribution of dysfunctional mental imagery to the onset or maintenance of de-
pression needs further investigation, including the unique contribution of the repre-
sentational format (i.e., imagery versus verbal) of intrusive negative cognitions and of
impoverished positive cognitions.
3. The potential role of adaptive mental imagery in contributing to boosting optimism and
resilience needs further investigation targeted at understanding underlying mechanisms
and developing new treatment approaches.
4. Future studies should explore new applications of how imagery may enhance current
treatments for depression, for example, by helping patients with depression to engage in
potentially rewarding behavioral activities.
5. Interdisciplinary work, for example, work bridging clinical psychology and neuroscience
in the investigation of imagery-related mechanisms in depression psychopathology, is
highly recommended.
DISCLOSURE STATEMENT
F. Raes is codeveloper of the MEST program. The other authors are not aware of any affiliations,
memberships, funding, or financial holdings that might be perceived as affecting the objectivity
of this review.
ACKNOWLEDGMENTS
E.A. Holmes and S.E. Blackwell are supported by the Medical Research Council (United Kingdom)
intramural program (MC-A060-5PR50). E.A. Holmes is supported by a Wellcome Trust Clin-
ical Fellowship (WT088217), and the National Institute for Health Research (NIHR) Oxford
Biomedical Research Center Program. The views expressed are those of the authors and not nec-
essarily those of the NHS, the NIHR or the Department of Health. S. Burnett Heyes is funded
by a British Academy postdoctoral research fellowship. F. Renner is supported by a postdoctoral
research fellowship from the German Academic Exchange Service (DAAD). F. Raes is supported
by KU Leuven Center for Excellence on Generalization Research (GRIPTT; PF/10/005). We
are grateful for discussion of these topics over time with wider members of the team including
Julie Ji, Tamara Lang, Arnaud Pictet, Michael Browning, and Catherine Deeprose.
LITERATURE CITED
Addis DR, Schacter DL. 2008. Constructive episodic simulation: Temporal distance and detail of past and
future events modulate hippocampal engagement. Hippocampus 18:227–37
Addis DR, Wong AT, Schacter DL. 2007. Remembering the past and imagining the future: common and
distinct neural substrates during event construction and elaboration. Neuropsychologia 45:1363–77
Am. Psychiatr. Assoc. 2013. Diagnostic and Statistical Manual of Mental Disorders. Washington, DC: Am.
Psychiatr. Publ. 5th ed.
www.annualreviews.org Mental Imagery in Depression 271
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Anderson RJ, Dewhurst SA, Nash RA. 2012. Shared cognitive processes underlying past and future thinking:
the impact of imagery and concurrent task demands on event specificity. J. Exp. Psychol.: Learn. Mem.
Cogn. 38:356–65
Anderson RJ, Evans GL. 2015. Mental time travel in dysphoria: differences in the content and subjective
experience of past and future episodes. Conscious. Cogn. 37:237–48
Anderson RJ, Goddard L, Powell JH. 2010. Reduced specificity of autobiographical memory as a moderator
of the relationship between daily hassles and depression. Cogn. Emot. 24:702–9
Anderson VA, Anderson P, Northam E, Jacobs R, Catroppa C. 2001. Development of executive functions
through late childhood and adolescence in an Australian sample. Dev. Neuropsychol. 20:385–406
Andrews G, Poulton R, Skoog I. 2005. Lifetime risk of depression: restricted to a minority or waiting for
most? Br.J.Psychiatry187:495–96
Baddeley AD, Andrade J. 2000. Working memory and the vividness of imagery. J. Exp. Psychol.: Gen. 129:126–
45
Bechtel W. 2009. Constructing a philosophy of science of cognitive science. Top. Cogn. Sci. 1:548–69
Beck AT, Haigh EAP. 2014. Advances in cognitive theory and therapy: the generic cognitive model. Annu.
Rev. Clin. Psychol. 10:1–24
Beck AT, Laude R, Bohnert M. 1974. Ideational components of anxiety neurosis. Arch. Gen. Psychiatry 31:319–
25
Beck AT, Rush JA, Shaw FB, Emery G. 1979. Cognitive Therapy of Depression. New York: Guilford
Bell T, Mackie L, Bennett-Levy J. 2015. “Venturing towards the dark side”: the use of imagery interventions
by recently qualified cognitive–behavioural therapists. Clin. Psychol. Psychother. 22:591–603
Benvenuti SM, Mennella R, Buodo G, Palomba D. 2015. Dysphoria is associated with reduced cardiac vagal
withdrawal during the imagery of pleasant scripts: evidence for the positive attenuation hypothesis. Biol.
Psychol. 106:28–38
Bergouignan L, Lemogne C, Foucher A, Longin E, Vistoli D, et al. 2008. Field perspective deficit for posi-
tive memories characterizes autobiographical memory in euthymic depressed patients. Behav. Res. Ther.
46:322–33
Birrer E, Michael T, Munsch S. 2007. Intrusive images in PTSD and in traumatised and non-traumatised
depressed patients: a cross-sectional clinical study. Behav. Res. Ther. 45:2053–65
Blackwell SE, Browning M, Mathews A, Pictet A, Welch J, et al. 2015. Positive imagery-based cognitive
bias modification as a web-based treatment tool for depressed adults: a randomized controlled trial. Clin.
Psychol. Sci. 3:91–111
Blackwell SE, Holmes EA. 2010. Modifying interpretation and imagination in clinical depression: a single
case series using cognitive bias modification. Appl. Cogn. Psychol. 24:338–50
Blackwell SE, Rius-Ottenheim N, Schulte-van Maaren YWM, Carlier IVE, Middelkoop VD, et al. 2013.
Optimism and mental imagery: a possible cognitive marker to promote well-being? Psychiatry Res. 206:56–
61
Bockting CL, Hollon SD, Jarrett RB, Kuyken W, Dobson K. 2015. A lifetime approach to major depressive
disorder: the contributions of psychological interventions in preventing relapse and recurrence. Clin.
Psychol. Rev. 41:16–26
Brewin CR, Gregory JD, Lipton M, Burgess N. 2010. Intrusive images in psychological disorders: character-
istics, neural mechanisms, and treatment implications. Psychol. Rev. 117:210–32
Brewin CR, Reynolds M, Tata P. 1999. Autobiographical memory processes and the course of depression.
J. Abnorm. Psychol. 108:511–17
Brewin CR, Watson M, McCarthy S, Hyman P, Dayson D. 1998. Intrusive memories and depression in cancer
patients. Behav. Res. Ther. 36:1131–42
Brewin CR, Wheatley J, Patel T, Fearon P, Hackmann A, et al. 2009. Imagery rescripting as a brief stand-alone
treatment for depressed patients with intrusive memories. Behav. Res. Ther. 47:569–76
Burnett Heyes S, Lau JYF, Holmes EA. 2013. Mental imagery, emotion and psychopathology across child
and adolescent development. Dev. Cogn. Neurosci. 5:119–33
Carver CS, Scheier MF. 2014. Dispositional optimism. Trends Cogn. Sci. 18:293–99
Carver CS, Scheier MF, Segerstrom SC. 2010. Optimism. Clin. Psychol. Rev. 30:879–89
272 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Caspi A, Moffitt TE, Newman DL, Silva PA. 1996. Behavioral observations at age 3 years predict adult
psychiatric disorders. Longitudinal evidence from a birth cohort. Arch. Gen. Psychiatry 53:1033–39
Chan CKY, Cameron LD. 2012. Promoting physical activity with goal-oriented mental imagery: a randomized
controlled trial. J. Behav. Med. 35:347–63
Chen J, Yang L-Q, Zhang Z-J, Ma W-T, Xing-qu W, et al. 2013a. The association between the disruption of
motor imagery and the number of depressive episodes of major depression. J. Affect. Disord. 150:337–43
Chen J, Yang L, Ma W, Wu X, Zhang Y, et al. 2013b. Ego-rotation and object-rotation in major depressive
disorder. Psychiatry Res. 209:32–39
Clark IA, Mackay CE, Woolrich MW, Holmes EA. 2016. Intrusive memories to traumatic footage: the neural
basis of their encoding and involuntary recall. Psychol. Med. 46:505–18
Clark IA, Niehaus KE, Duff EP, Di Simplicio MC, Clifford GD, et al. 2014. First steps in using machine
learning on fMRI data to predict intrusive memories of traumatic film footage. Behav. Res. Ther. 62:37–46
Cocude M, Charlot V, Denis M. 1997. Latency and duration of visual mental images in normal and depressed
subjects. J. Ment. Imag. 21:127–42
Conway MA, Loveday C. 2015. Remembering, imagining, false memories and personal meanings. Conscious.
Cogn. 33:574–81
Conway MA, Pleydell-Pearce CW. 2000. The construction of autobiographical memories in the self-memory
system. Psychol. Rev. 107:261–88
Crane C, Heron J, Gunnell D, Lewis G, Evans J, Williams JM. 2016. Adolescent over-general memory, life
events and mental health outcomes: findings from a UK cohort study. Memory 24:348–63
Crane C, Shah D, Barnhofer T, Holmes EA. 2012. Suicidal imagery in a previously depressed community
sample. Clin. Psychol. Psychother. 19:57–69
Craske MG. 2014. Introduction to special issue: How does neuroscience inform psychological treatment?
Behav. Res. Ther. 62:1–2
Cristea IA, Kok RN, Cuijpers P. 2015. Efficacy of cognitive bias modification interventions in anxiety and
depression: meta-analysis. Br.J.Psychiatry206:7–16
Cuijpers P, Karyotaki E, Weitz E, Andersson G, Hollon SD, van Straten A. 2014. The effects of psychother-
apies for major depression in adults on remission, recovery and improvement: a meta-analysis. J. Affect.
Disord. 159:118–26
Cuijpers P, Sijbrandij M, Koole SL, Andersson G, Beekman AT, Reynolds CF. 2013. The efficacy of psy-
chotherapy and pharmacotherapy in treating depressive and anxiety disorders: a meta-analysis of direct
comparisons. World Psychiatry 12:137–48
D’Argembeau A, Van der Linden M. 2012. Predicting the phenomenology of episodic future thoughts. Con-
scious. Cogn. 21:1198–206
Dalgleish T, Bevan A, McKinnon A, Breakwell L, Mueller V, et al. 2014. A comparison of MEmory Specificity
Training (MEST) to education and support (ES) in the treatment of recurrent depression: study protocol
for a cluster randomised controlled trial. Trials 15:293
Dalgleish T, Navrady L, Bird E, Hill E, Dunn BD, Golden A. 2013. Method-of-loci as a mnemonic device
to facilitate access to self-affirming personal memories for individuals with depression. Clin.Psychol.Sci.
1:156–62
Dalgleish T, Werner-Seidler A. 2014. Disruptions in autobiographical memory processing in depression and
the emergence of memory therapeutics. Trends Cogn. Sci. 18:596–604
Davey CG, Y ¨
ucel M, Allen NB. 2008. The emergence of depression in adolescence: development of the
prefrontal cortex and the representation of reward. Neurosci. Biobehav. Rev. 32:1–19
Duncan LR, Hall CR, Wilson PM, Rodgers WM. 2012. The use of a mental imagery intervention to enhance
integrated regulation for exercise among women commencing an exercise program. Motiv. Emot. 36:452–
64
Dunn BD. 2012. Helping depressed clients reconnect to positive emotional experience: current insights and
future directions. Clin. Psychol. Psychother. 19:326–40
Eardley AF, Pring L. 2006. Remembering the past and imagining the future: a role for nonvisual imagery in
the everyday cognition of blind and sighted people. Memory 14:925–36
Edwards D. 2007. Restructuring implicational meaning through memory-based imagery: some historical
notes. J. Behav. Ther. Exp. Psychiatry 38:306–16
www.annualreviews.org Mental Imagery in Depression 273
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Eigenhuis E, Seldenrijk A, van Schaik A, Raes F, van Oppen P. 2015. Feasibility and effectiveness of memory
specificity training in depressed outpatients: a pilot study. Clin. Psychol. Psychother. In press
Everaert J, Koster EHW, Derakshan N. 2012. The combined cognitive bias hypothesis in depression. Clin.
Psychol. Rev. 32:413–24
Fredrickson BL, Joiner T. 2002. Positive emotions trigger upward spirals toward emotional well-being. Psychol.
Sci. 13:172–75
Fresco DM, Frankel AN, Mennin DS, Turk CL, Heimberg RG. 2002. Distinct and overlapping features of
rumination and worry: the relationship of cognitive production to negative affective states. Cogn. Ther.
Res. 26:179–88
Galton F. 1883. Inquiries into Human Faculty and Its Development. London: Dent
Gilbert P. 2009. The Compassionate Mind. London: Constable & Robinson
G¨
orgen SM, Joormann J, Hiller W, Witth ¨
oft M. 2015. The role of mental imagery in depression: Negative
mental imagery induces strong implicit and explicit affect in depression. Front. Psychiatry 6:94
Gosden T, Morris PG, Ferreira NB, Grady C, Gillanders DT. 2014. Mental imagery in chronic pain: preva-
lence and characteristics. Eur. J. Pain 18:721–28
Gotlib IH, Joormann J. 2010. Cognition and depression: current status and future directions. Annu. Rev. Clin.
Psychol. 6:285–32
Gregory A, Eley T. 2007. Genetic influences on anxiety in children: what we’ve learned and where we’re
heading. Clin. Child Fam. Psychol. Rev. 10:199–212
Hach S, Tippett LJ, Addis DR. 2014. Neural changes associated with the generation of specific past and future
events in depression. Neuropsychologia 65:41–55
Hagenaars MA, Holmes EA. 2012. Mental imagery in psychopathology: another step; editorial for the special
issue of Journal of Experimental Psychopathology.J. Exp. Psychopathol. 3:121–26
Hales SA, Blackwell SE, Di Simplicio M, Iyadurai L, Young K, Holmes EA. 2014. Imagery-based cognitive-
behavioral assessment. In Assessment in Cognitive Therapy, ed. GP Brown, DA Clark, pp. 69–93. New
York: Guilford
Hales SA, Deeprose C, Goodwin GM, Holmes EA. 2011. Cognitions in bipolar disorder versus unipolar
depression: imagining suicide. Bipolar Disord. 13:651–61
Haque S, Juliana E, Khan R, Hasking P. 2014. Autobiographical memory and hierarchical search strategies
in depressed and non-depressed participants. BMC Psychiatry 14:310
Harris PL. 2000. The Work of the Imagination. Oxford, UK: Wiley-Blackwell
Hauer BJ, Wessel I, Geraerts E, Merckelbach H, Dalgleish T. 2008. Autobiographical memory specificity after
manipulating retrieval cues in adults reporting childhood sexual abuse. J. Abnorm. Psychol. 117:444–53
Hauser TU, Iannaccone R, Walitza S, Brandeis D, Brem S. 2015. Cognitive flexibility in adolescence: neural
and behavioral mechanisms of reward prediction error processing in adaptive decision making during
development. NeuroImage 104:347–54
Hipwell AE, Sapotichne B, Klostermann S, Battista D, Keenan K. 2011. Autobiographical memory as a
predictor of depression vulnerability in girls. J. Clin. Child Adolesc. Psychol. 40:254–65
Hirsch CR, Clark DM, Mathews A. 2006. Imagery and interpretations in social phobia: support for the
combined cognitive biases hypothesis. Behav. Ther. 37:223–36
Hirsch CR, Clark DM, Mathews A, Williams R. 2003. Self-images play a causal role in social phobia. Behav.
Res. Ther. 41:909–21
Hollon SD, Stewart MO, Strunk D. 2006. Enduring effects for cognitive behavior therapy in the treatment
of depression and anxiety. Annu. Rev. Psychol. 57:285–315
Holmes EA, Arntz A, Smucker MR. 2007a. Imagery rescripting in cognitive behaviour therapy: images,
treatment techniques and outcomes. J. Behav. Ther. Exp. Psychiatry 38:297–305
Holmes EA, Coughtrey AE, Connor A. 2008a. Looking at or through rose-tinted glasses? Imagery perspective
and positive mood. Emotion 8:875–79
Holmes EA, Crane C, Fennell MJV, Williams JMG. 2007b. Imagery about suicide in depression—“flash-
forwards”? J. Behav. Ther. Exp. Psychiatry 38:423–34
Holmes EA, Craske MG, Graybiel AM. 2014. Psychological treatments: a call for mental-health science.
Clinicians and neuroscientists must work together to understand and improve psychological treatments.
Nature 511:287–89
274 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Holmes EA, Hackmann A. 2004. A healthy imagination? Editorial for the special issue of Memory: mental
imagery and memory in psychopathology. Memory 12:387–88
Holmes EA, Lang TJ, Deeprose C. 2009a. Mental imagery and emotion in treatment across disorders: using
the example of depression. Cogn. Behav. Ther. 38:21–28
Holmes EA, Lang TJ, Moulds ML, Steele AM. 2008b. Prospective and positive mental imagery deficits in
dysphoria. Behav. Res. Ther. 46:976–81
Holmes EA, Lang TJ, Shah DM. 2009b. Developing interpretation bias modification as a “cognitive vaccine”
for depressed mood: Imagining positive events makes you feel better than thinking about them verbally.
J. Abnorm. Psychol. 118:76–88
Holmes EA, Mathews A. 2005. Mental imagery and emotion: a special relationship? Emotion 5:489–97
Holmes EA, Mathews A. 2010. Mental imagery in emotion and emotional disorders. Clin.Psychol.Rev.30:349–
62
Holmes EA, Mathews A, Dalgleish T, Mackintosh B. 2006. Positive interpretation training: effects of mental
imagery versus verbal training on positive mood. Behav. Ther. 37:237–47
Holmes EA, Mathews A, Mackintosh B, Dalgleish T. 2008c. The causal effect of mental imagery on emotion
assessed using picture-word cues. Emotion 8:395–409
Ivins A, Di Simplicio M, Close H, Goodwin GM, Holmes EA. 2014. Mental imagery in bipolar affective
disorder versus unipolar depression: investigating cognitions at times of “positive” mood. J. Affect. Disord.
166:234–42
Ji JL, Burnett Heyes S, MacLeod C, Holmes EA. 2015. Emotional mental imagery as simulation of reality:
fear and beyond—a tribute to Peter Lang. Behav. Ther. In press
Joh AS, Jaswal VK, Keen R. 2011. Imagining a way out of the gravity bias: Preschoolers can visualize the
solution to a spatial problem. Child Dev. 82:744–50
Joormann J, Siemer M, Gotlib IH. 2007. Mood regulation in depression: differential effects of distraction and
recall of happy memories on sad mood. J. Abnorm. Psychol. 113:179–88
Kandris E, Moulds ML. 2008. Can imaginal exposure reduce intrusive memories in depression? A case study.
Cogn. Behav. Ther. 37:216–20
Kazdin AE. 2007. Mediators and mechanisms of change in psychotherapy research. Annu. Rev. Clin. Psychol.
3:1–27
Kessler RC, Avenevoli S, Costello J, Greif Green J, Gruber MJ, et al. 2012. Severity of 12-month DSM-IV
disorders in the National Comorbidity Survey Replication Adolescent Supplement. Arch. Gen. Psychiatry
69:381–89
Kessler RC, Berglund P, Demler O, Jin R, Merikangas KR, Walters EE. 2005. Lifetime prevalence and age-
of-onset distributions of DSM-IV disorders in the national comorbidity survey replication. Arch. Gen.
Psychiatry 62:593–602
Kessler RC, McGonagle KA, Zhao SY, Nelson CB, Hughes M, et al. 1994. Lifetime and 12-month prevalence
of DSM-III-R psychiatric disorders in the United States: results from the National Comorbidity Survey.
Arch. Gen. Psychiatry 51:8–19
Kleim B, Ehlers A. 2008. Reduced autobiographical memory specificity predicts depression and posttraumatic
stress disorder after recent trauma. J. Consult. Clin. Psychol. 76:231–42
Kleim B, Graham B, Fihosy S, Stott R, Ehlers A. 2014a. Reduced specificity in episodic future thinking in
posttraumatic stress disorder. Clin. Psychol. Sci. 2:165–73
Kleim B, Th¨
orn HA, Ehlert U. 2014b. Positive interpretation bias predicts well-being in medical interns.
Front. Psychol. 5:640
Kn¨
auper B, McCollam A, Rosen-Brown A, Lacaille J, Kelso E, Roseman M. 2011. Fruitful plans: Adding tar-
geted mental imagery to implementation intentions increases fruit consumption. Psychol. Health 26:601–17
Kosslyn SM. 1996. Image and Brain: The Resolution of the Imagery Debate. Cambridge, MA: MIT Press
Kosslyn SM, Brunn J, Cave KR, Wallach RW. 1984. Individual differences in mental-imagery ability: a
computational analysis. Cognition 18:195–243
Kosslyn SM, Ganis G, Thompson WL. 2001. Neural foundations of imagery. Nat. Rev. Neurosci. 2:635–42
Kosslyn SM, Thompson WL, Ganis G. 2006. The Case for Mental Imagery. New York: Oxford Univ. Press
Kraemer HC, Kazdin AE, Offord DR, Kessler RC, Jensen PS, Kupfer DJ. 1997. Coming to terms with the
terms of risk. Arch. Gen. Psychiatry 54:337–43
www.annualreviews.org Mental Imagery in Depression 275
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Krans J. 2011. Introduction to the special issue: intrusive imagery in psychopathology. New research findings,
implications for theory and treatment, and future directions. Int. J. Cogn. Ther. 4:117–21
Kuyken W, Brewin CR. 1994. Intrusive memories of childhood abuse during depressive episodes. Behav. Res.
Ther. 32:525–28
Kuyken W, Brewin CR. 1995. Autobiographical memory functioning in depression and reports of early abuse.
J. Abnorm. Psychol. 104:585–91
Kuyken W, Howell R. 2006. Facets of autobiographical memory in adolescents with major depressive disorder
and never-depressed controls. Cogn. Emot. 20:466–87
Kuyken W, Moulds ML. 2009. Remembering as an observer: How is autobiographical memory retrieval
vantage perspective linked to depression? Memory 17:624–34
Lang PJ. 1977. Imagery in therapy: an information processing analysis of fear. Behav. Ther. 8:862–86
Lang PJ. 1979. A bio-informational theory of emotional imagery. Psychophysiology 16:495–512
Lang PJ, Kozak MJ, Miller GA, Levin DN, McLean A. 1980. Emotional imagery: conceptual structure and
pattern of somato-visceral response. Psychophysiology 17:179–92
Lang TJ, Blackwell SE, Harmer CJ, Davison P, Holmes EA. 2012. Cognitive bias modification using mental
imagery for depression: developing a novel computerized intervention to change negative thinking styles.
Eur. J. Personal. 26:145–57
Lang TJ, Moulds ML, Holmes EA. 2009. Reducing depressive intrusions via a computerized cognitive bias
modification of appraisals task: developing a cognitive vaccine. Behav. Res. Ther. 47:139–45
Lee DA. 2005. The perfect nurturer: a model to develop a compassionate mind within the context of cognitive
therapy. In Compassion: Conceptualisations, Research and Use in Psychothrapy, ed. IP Gilbert, pp. 326–51.
London: Routledge
Lemogne C, Piolino P, Friszer S, Astrid C, Nathalie GB, et al. 2006. Episodic autobiographical memory in
depression: specificity, autonoetic consciousness, and self-perspective. Conscious. Cogn. 15:258–68
Linden DEJ, Habes I, Johnston SJ, Linden S, Tatineni R, et al. 2012. Real-time self-regulation of emotion
networks in patients with depression. PLOS ONE 7:e38115
Loft MH, Cameron LD. 2013. Using mental imagery to deliver self-regulation techniques to improve sleep
behaviors. Ann. Behav. Med. 46:260–72
Luna B, Garver KE, Urban TA, Lazar NA, Sweeney JA. 2004. Maturation of cognitive processes from late
childhood to adulthood. Child Dev. 75:1357–72
Maccallum F, Bryant RA. 2011. Imagining the future in complicated grief. Depress. Anxiety 28:658–65
MacLeod AK, Moore R. 2000. Positive thinking revisited: positive cognitions, well-being and mental health.
Clin. Psychol. Psychother. 7:1–10
Madore KP, Gaesser B, Schacter DL. 2014. Constructive episodic simulation: dissociable effects of a specificity
induction on remembering, imagining, and describing in young and older adults. J. Exp. Psychol.: Learn.
Mem. Cogn. 40:609–22
Madore KP, Schacter DL. 2015. Remembering the past and imagining the future: selective effects of an
episodic specificity induction on detail generation. Q. J. Exp. Psychol. (Hove). In press
Malogiannis IA, Arntz A, Spyropoulou A, Tsartsara E, Aggeli A, et al. 2014. Schema therapy for patients with
chronic depression: a single case series study. J. Behav. Ther. Exp. Psychiatry 45:319–29
Mansell W, Lam D. 2004. A preliminary study of autobiographical memory in remitted bipolar and unipolar
depression and the role of imagery in the specificity of memory. Memory 12:437–46
Martell CR, Dimidjian S, Herman-Dunn R. 2010. Behavioral Activation for Depression: A Clinician’s Guide.New
York: Guilford
McIsaac HK, Eich E. 2002. Vantage point in episodic memory. Psychon. Bull. Rev. 9:146–50
McIsaac HK, Eich E. 2004. Vantage point in traumatic memory. Psychol. Sci. 15:248–53
Meevissen YMC, Peters ML, Alberts HJEM. 2011. Become more optimistic by imagining a best possible self:
effects of a two week intervention. J. Behav. Ther. Exp. Psychiatry 42:371–78
Miller GA, Levin DN, Kozak MJ, Cook EW, McLean A, Lang PJ. 1987. Individual differences in imagery
and the psychophysiology of emotion. Cogn. Emot. 1:367–90
Mischel W, Shoda Y, Rodriguez MI. 1989. Delay of gratification in children. Science 244:933–38
Mogoas¸e C, Brailean A, David D. 2013. Can concreteness training alone reduce depressive symptoms? A
randomized pilot study using an Internet-delivered protocol. Cogn. Ther. Res. 37:704–12
276 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Morina N, Deeprose C, Pusowski C, Schmid M, Holmes EA. 2011. Prospective mental imagery in patients
with major depressive disorder or anxiety disorders. J. Anxiety Disord. 25:1032–37
Moritz S, Hormann CC, Schroder J, Berger T, Jacob GA, et al. 2014. Beyond words: sensory properties of
depressive thoughts. Cogn. Emot. 28:1047–56
Morton J, Frith U. 1995. Causal modelling: a structural approach to developmental psychology. In Develop-
mental Psychopathology,Vol.1:Theory and Methods. New York: Wiley
Moussavi S, Chatterji S, Verdes E, Tandon A, Patel V, Ustun B. 2007. Depression, chronic diseases, and
decrements in health: results from the World Health Surveys. Lancet 370:851–58
Natl. Inst. Health Clin. Excell. 2005. Post-Traumatic Stress Disorder (PTSD): The Management of PTSD in
Adults and Children in Primary and Secondary Care. Leicester, UK: Gaskell
Natl. Inst. Health Clin. Excell. 2009. Depression: The Treatment and Management of Depression in Adults (Update).
London: Natl. Inst. Health Clin. Excell.
Natl. Inst. Health Clin. Excell. 2013. Post-Traumatic Stress Disorder (PTSD): Evidence Update December 2013.
Manchester, UK: Natl. Inst. Health Clin. Excell.
Natl. Inst. Ment. Health. 2014. NIMH Clinical Trials Funding Opportunity Announcements—Applicant FAQs.
Bethesda, MD: Natl. Inst. Ment. Health
Nelis S, Debeer E, Holmes EA, Raes F. 2013. Dysphoric students show higher use of the observer perspective
in their retrieval of positive versus negative autobiographical memories. Memory 21:423–30
Nelis S, Holmes EA, Palmieri R, Bellelli G, Raes F. 2015. Thinking back about a positive event: the impact
of processing style on positive affect. Front. Psychiatry 6:3
Nelis S, Vanbrabant K, Holmes EA, Raes F. 2012. Greater positive affect change after mental imagery than
verbal thinking in a student sample. J. Exp. Psychopathol. 3:178–88
Neshat-Doost HT, Dalgleish T, Yule W, Kalantari M, Ahmadi SJ, et al. 2012. Enhancing autobiographi-
cal memory specificity through cognitive training: an intervention for depression translated from basic
science. Clin. Psychol. Sci. 1:84–92
Newby JM, Moulds ML. 2011a. Characteristics of intrusive memories in a community sample of depressed,
recovered depressed and never-depressed individuals. Behav. Res. Ther. 49:234–43
Newby JM, Moulds ML. 2011b. Do intrusive memory characteristics predict depression at 6 months? Memory
19:538–46
Nigro G, Neisser U. 1983. Point of view in personal memories. Cogn. Psychol. 15:467–82
Nolen-Hoeksema S. 1998. Ruminative coping with depression. In Motivation and Self-Regulation Across the Life
Span, ed. J Heckhausen, CS Dweck, pp. 237–56. New York: Cambridge Univ. Press
Ormel J, Raven D, van Oort F, Hartman CA, Reijneveld SA, et al. 2014. Mental health in Dutch adolescents:
a TRAILS report on prevalence, severity, age of onset, continuity and co-morbidity of DSM disorders.
Psychol. Med. 45:345–60
Patel T, Brewin CR, Wheatley J, Wells A, Fisher P, Myers S. 2007. Intrusive images and memories in major
depression. Behav. Res. Ther. 45:2573–80
Patron E, Benvenuti SM, Favretto G, Gasparotto R, Palomba D. 2015. Depression is associated with increased
vagal withdrawal during unpleasant emotional imagery after cardiac surgery. Auton. Neurosci. 189:75–82
Paus T, Keshavan M, Giedd JN. 2008. Why do many psychiatric disorders emerge during adolescence? Nat.
Rev. Neurosci. 9:947–57
Pearson DG, Deeprose C, Wallace-Hadrill SMA, Burnett Heyes S, Holmes EA. 2013. Assessing mental
imagery in clinical psychology: a review of imagery measures and a guiding framework. Clin. Psychol. Rev.
33:1–23
Pearson J, Naselaris T, Holmes EA, Kosslyn SM. 2015. Mental imagery: functional mechanisms and clinical
applications. Trends Cogn. Sci. 19:590–602
Pictet A, Coughtrey AE, Mathews A, Holmes EA. 2011. Fishing for happiness: the effects of positive imagery
on interpretation bias and a behavioral task. Behav. Res. Ther. 49:885–91
Pizzagalli DA. 2014. Depression, stress, and anhedonia: toward a synthesis and integrated model. Annu. Rev.
Clin. Psychol. 10:393–423
Raes F, Hermans D, Williams JMG, Beyers W, Brunfaut E, Eelen P. 2006. Reduced autobiographical memory
specificity and rumination in predicting the course of depression. J. Abnorm. Psychol. 115:699–704
www.annualreviews.org Mental Imagery in Depression 277
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Raes F, Hermans D, Williams JMG, Demyttenaere K, Sabbe B, et al. 2005. Reduced specificity of autobio-
graphical memories: a mediator between rumination and ineffective problem-solving in major depression?
J. Affect. Disord. 87:331–35
Raes F, Williams JG, Hermans D. 2009. Reducing cognitive vulnerability to depression: a preliminary investi-
gation of Memory Specificity Training (MEST) in inpatients with depressive symptomatology. J. Behav.
Ther. Exp. Psychiatry 40:24–38
Ramirez S, Liu X, MacDonald CJ, Moffa A, Zhou J, et al. 2015. Activating positive memory engrams suppresses
depression-like behaviour. Nature 522:335–39
Rasmussen KW, Berntsen D. 2014. “I can see clearly now”: the effect of cue imageability on mental time
travel. Mem. Cogn. 42:1063–75
Renner F, Arntz A, Leeuw I, Huibers MJH. 2013. Treatment for chronic depression using schema therapy.
Clin. Psychol. Sci. Pract. 20:166–80
Renner F, Arntz A, Peeters FP, Lobbestael J, Huibers MJH. 2016. Schema therapy for chronic depression:
results of a multiple single case series study. J. Behav. Ther. Exp. Psychiatry 51:66–73
Reynolds M, Brewin CR. 1999. Intrusive memories in depression and posttraumatic stress disorder. Behav.
Res. Ther. 37:201–15
Robinaugh DJ, McNally RJ. 2013. Remembering the past and envisioning the future in bereaved adults with
and without complicated grief. Clin. Psychol. Sci. 1:290–300
Roiser JP. 2015. What has neuroscience ever done for us? Psychologist 28:284–87
Roiser JP, Elliott R, Sahakian BJ. 2012. Cognitive mechanisms of treatment in depression. Neuropsychophar-
macology 37:117–36
Rutter M. 1984. Psychopathology and development: I. Childhood antecedents of adult psychiatric disorder.
Aust. N. Z. J. Psychiatry 18:225–34
Schacter DL. 2013. Memory: from the laboratory to everyday life. Dialogues Clin. Neurosci. 15:393–95
Schacter DL, Addis DR. 2007. The cognitive neuroscience of constructive memory: remembering the past
and imagining the future. Philos. Trans. R. Soc. B 362:773–86
Schacter DL, Addis DR, Hassabis D, Martin VC, Spreng RN, Szpunar KK. 2012. The future of memory:
remembering, imagining, and the brain. Neuron 76:677–94
Scott J, Stanton B, Garland A, Ferrier IN. 2000. Cognitive vulnerability in patients with bipolar disorder.
Psychol. Med. 30:467–72
Selby EA, Anestis MD, Joiner TE. 2007. Daydreaming about death: violent daydreaming as a form of emotion
dysregulation in suicidality. Behav. Modif. 31:867–79
Sharot T, Riccardi AM, Raio CM, Phelps EA. 2007. Neural mechanisms mediating optimism bias. Nature
450:102–5
Southwick SM, Charney DS. 2012. The science of resilience: implications for the prevention and treatment
of depression. Science 338:79–82
Spinhoven P, Bockting CL, Schene AH, Koeter MW, Wekking EM, Williams JM. 2006. Autobiographical
memory in the euthymic phase of recurrent depression. J. Abnorm. Psychol. 115:590–600
Stawarczyk D, D’Argembeau A. 2015. Neural correlates of personal goal processing during episodic future
thinking and mind-wandering: an ALE meta-analysis. Hum. Brain Mapp. 36:2928–47
Steinberg L. 2005. Cognitive and affective development in adolescence. Trends Cogn. Sci. 9:69–74
Stevenson CE, Kleibeuker SW, De Dreu C, Crone EA. 2014. Training creative cognition: adolescence as a
flexible period for improving creativity. Front. Hum. Neurosci. 8:827
St ¨
ober J. 2000. Prospective cognitions in anxiety and depression: replication and methodological extension.
Cogn. Emot. 14:725–29
Stopa L. 2011. Special series. Imagery rescripting across disorders: a practical guide. Cogn. Behav. Pract.
18:421–23
Sumner JA, Griffith JW, Mineka S. 2010. Overgeneral autobiographical memory as a predictor of the course
of depression: a meta-analysis. Behav. Res. Ther. 48:614–25
Sumner JA, Griffith JW, Mineka S, Newcomb Rekart K, Zinbarg RE, Craske MG. 2011. Overgeneral autobio-
graphical memory and chronic interpersonal stress as predictors of the course of depression in adolescents.
Cogn. Emot. 25:183–92
278 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Sumner JA, Mineka S, Adam EK, Craske MG, Vreshek-Schallhorn S, et al. 2014. Testing the CaR-FA-X
model: investigating the mechanisms underlying reduced autobiographical memory specificity in indi-
viduals with and without a history of depression. J. Abnorm. Psychol. 123:471–86
Sz ˝
oll ˝
osi ´
A, Pajkossy P, Racsm´
any M. 2015. Depressive symptoms are associated with the phenomenal char-
acteristics of imagined positive and negative future events. Appl. Cogn. Psychol. 29:762–67
Szpunar KK, Schacter DL. 2013. Get real: effects of repeated simulation and emotion on the perceived
plausibility of future experience. J. Exp. Psychol.: Gen. 142:323–27
Torkan H, Blackwell SE, Holmes EA, Kalantari M, Neshat-Doost HT, et al. 2014. Positive imagery cognitive
bias modification in treatment-seeking patients with major depression in Iran: a pilot study. Cogn. Ther.
Res. 38:132–45
Van Daele T, Griffith JW, Van den Bergh O, Hermans D. 2014. Overgeneral autobiographical memory
predicts changes in depression in a community sample. Cogn. Emot. 28:1303–12
van der Schaaf ME, Warmerdam E, Crone EA, Cools R. 2011. Distinct linear and non-linear trajectories of
reward and punishment reversal learning during development: relevance for dopamine’s role in adolescent
decision making. Dev. Cogn. Neurosci. 1:578–90
Vella NC, Moulds ML. 2013. The impact of shifting vantage perspective when recalling and imagining positive
events. Memory 22:256–64
Vos T, Flaxman AD, Naghavi M, Lozano R, Michaud C, et al. 2012. Years lived with disability (YLDs) for
1160 sequelae of 289 diseases and injuries 1990–2010: a systematic analysis for the Global Burden of
Disease Study 2010. Lancet 380:2163–96
Watkins ER, Baeyens CB, Read R. 2009. Concreteness training reduces dysphoria: proof-of-principle for
repeated cognitive bias modification in depression. J. Abnorm. Psychol. 118:55–64
Watkins ER, Moberly NJ. 2009. Concreteness training reduces dysphoria: a pilot proof-of-principle study.
Behav. Res. Ther. 47:48–53
Watkins ER, Taylor RS, Byng R, Baeyens C, Read R, et al. 2012. Guided self-help concreteness training as an
intervention for major depression in primary care: a Phase II randomized controlled trial. Psychol. Med.
42:1359–71
Weil LG, Fleming SM, Dumontheil I, Kilford EJ, Weis RS, et al. 2013. The development of metacognitive
ability in adolescence. Conscious. Cogn. 22:264–71
Wells A, Fisher P, Myers S, Wheatley J, Patel T, Brewin CR. 2009. Metacognitive therapy in recurrent and
persistent depression: a multiple-baseline study of a new treatment. Cogn. Ther. Res. 33:291–300
Werner-Seidler A, Moulds ML. 2011. Autobiographical memory characteristics in depression vulnerability:
Formerly depressed individuals recall less vivid positive memories. Cogn. Emot. 25:1087–103
Werner-Seidler A, Moulds ML. 2012a. Characteristics of self-defining memory in depression vulnerability.
Memory 20:935–48
Werner-Seidler A, Moulds ML. 2012b. Mood repair and processing mode in depression. Emotion 12:470–78
Werner-Seidler A, Moulds ML. 2014. Recalling positive self-defining memories in depression: the impact of
processing mode. Memory 22:525–35
Weßlau C, Steil R. 2014. Visual mental imagery in psychopathology—implications for the maintenance and
treatment of depression. Clin. Psychol. Rev. 34:273–81
Wheatley J, Brewin CR, Patel T, Hackmann A, Wells A, et al. 2007. “I’ll believe it when I see it”: imagery
rescripting of intrusive sensory memories in depression. J. Behav. Ther. Exp. Psychiatry 38:371–85
Wild J, Hackmann A, Clark DM. 2007. When the present visits the past: updating traumatic memories in
social phobia. J. Behav. Ther. Exp. Psychiatry 38:386–401
Williams AD, Blackwell SE, Mackenzie A, Holmes EA, Andrews G. 2013. Combining imagination and reason
in the treatment of depression: a randomized controlled trial of Internet-based cognitive bias modification
and Internet-CBT for depression. J. Consult. Clin. Psychol. 81:793–99
Williams AD, Moulds ML. 2007. Cognitive avoidance of intrusive memories: recall vantage perspectives
associations with depression. Behav. Res. Ther. 45:1145–53
Williams AD, Moulds ML. 2008. Manipulating recall vantage perspective of intrusive memories in dysphoria.
Memory 16:742–50
www.annualreviews.org Mental Imagery in Depression 279
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12CH10-Holmes ARI 12 February 2016 15:47
Williams AD, O’Moore K, Blackwell SE, Smith J, Holmes EA, Andrews G. 2015. Positive imagery cogni-
tive bias modification (CBM) and Internet-based cognitive behavioural therapy (iCBT): a randomized
controlled trial. J. Affect. Disord. 178:131–41
Williams JMG, Barnhofer T, Crane C, Beck AT. 2005. Problem solving deteriorates following mood challenge
in formerly depressed patients with a history of suicidal ideation. J. Abnorm. Psychol. 114:421–31
Williams JMG, Barnhofer T, Crane C, Herman D, Raes F, et al. 2007. Autobiographical memory specificity
and emotional disorder. Psychol. Bull. 133:122–48
Williams JMG, Broadbent K. 1986. Autobiographical memory in suicide attempters. J. Abnorm. Psychol.
95:144–49
Williams JMG, Chan S, Crane C, Barnhofer T, Eade J, Healy H. 2006. Retrieval of autobiographical memories:
the mechanisms and consequences of truncated search. Cogn. Emot. 20:351–82
Williams JMG, Ellis NC, Tyers C, Healy H, Rose G, MacLeod AK. 1996. The specificity of autobiographical
memory and imageability of the future. Mem. Cogn. 24:116–25
Williams JMG, Healy HG, Ellis NC. 1999. The effect of imageability and predicability of cues in autobio-
graphical memory. Q. J. Exp. Psychol. A 52:555–79
Young JE, Klosko JS, Weishaar ME. 2003. Schema Therapy: A Practitioner’s Guide.NewYork:Guilford
Zarrinpar A, Deldin P, Kosslyn SM. 2006. Effects of depression on sensory/motor versus central processing
in visual mental imagery. Cogn. Emot. 20:737–58
280 Holmes et al.
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12-FrontMatter ARI 2 March 2016 14:46
Annual Review of
Clinical Psychology
Volume 12, 2016
Contents
The Efficacy of Exposure Therapy for Anxiety-Related Disorders and
Its Underlying Mechanisms: The Case of OCD and PTSD
Edna B. Foa and Carmen P. McLean pppppppppppppppppppppppppppppppppppppppppppppppppppppppp1
History of the Concept of Addiction
Peter E. Nathan, Mandy Conrad, and Anne Helene Skinstad ppppppppppppppppppppppppppppp29
Conducting Clinical Research Using Crowdsourced Convenience
Samples
Jesse Chandler and Danielle Shapiro pppppppppppppppppppppppppppppppppppppppppppppppppppppppp53
Computerized Adaptive Diagnosis and Testing of Mental Health
Disorders
Robert D. Gibbons, David J. Weiss, Ellen Frank, and David Kupfer ppppppppppppppppppppp83
Diagnostic Issues and Controversies in DSM-5: Return of the False
Positives Problem
Jerome C. Wakefield pppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppp105
The Importance of Considering Clinical Utility in the Construction of
a Diagnostic Manual
Stephanie N. Mullins-Sweatt, Gregory J. Lengel, and Hilary L. DeShong pppppppppppp133
Internet-Delivered Psychological Treatments
Gerhard Andersson ppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppp157
Developmental Demands of Cognitive Behavioral Therapy for
Depression in Children and Adolescents: Cognitive, Social,
and Emotional Processes
Judy Garber, Sarah A. Frankel, and Catherine G. Herrington ppppppppppppppppppppppppp181
Gender Dysphoria in Adults
Kenneth J. Zucker, Anne A. Lawrence, and Baudewijntje P.C. Kreukels ppppppppppppppp217
Mental Imagery in Depression: Phenomenology, Potential
Mechanisms, and Treatment Implications
Emily A. Holmes, Simon E. Blackwell, Stephanie Burnett Heyes, Fritz Renner,
and Filip Raes pppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppp249
vii
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
CP12-FrontMatter ARI 2 March 2016 14:46
Resolving Ambiguity in Emotional Disorders: The Nature and Role of
Interpretation Biases
Colette R. Hirsch, Frances Meeten, Charlotte Krah´e, and Clare Reeder ppppppppppppppppp281
Suicide, Suicide Attempts, and Suicidal Ideation
E. David Klonsky, Alexis M. May, and Boaz Y. Saffer pppppppppppppppppppppppppppppppppp307
The Neurobiology of Intervention and Prevention in Early Adversity
Philip A. Fisher, Kate G. Beauchamp, Leslie E. Roos, Laura K. Noll,
Jessica Flannery, and Brianna C. Delker pppppppppppppppppppppppppppppppppppppppppppppp331
Interactive and Mediational Etiologic Models of Eating Disorder
Onset: Evidence from Prospective Studies
Eric Stice pppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppp359
Paraphilias in the DSM-5
Anthony R. Beech, Michael H. Miner, and David Thornton pppppppppppppppppppppppppppp383
The Role of Craving in Substance Use Disorders: Theoretical and
Methodological Issues
Michael A. Sayette pppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppppp407
Clashing Diagnostic Approaches: DSM-ICD Versus RDoC
Scott O. Lilienfeld and Michael T. Treadway ppppppppppppppppppppppppppppppppppppppppppppp435
Mental Health in Lesbian, Gay, Bisexual, and Transgender (LGBT)
Youth
Stephen T. Russell and Jessica N. Fish ppppppppppppppppppppppppppppppppppppppppppppppppppppp465
Risk Assessment in Criminal Sentencing
John Monahan and Jennifer L. Skeem pppppppppppppppppppppppppppppppppppppppppppppppppppp489
The Relevance of the Affordable Care Act for Improving Mental
Health Care
David Mechanic and Mark Olfson pppppppppppppppppppppppppppppppppppppppppppppppppppppppp515
Indexes
Cumulative Index of Contributing Authors, Volumes 3–12 pppppppppppppppppppppppppppp543
Cumulative Index of Article Titles, Volumes 3–12 ppppppppppppppppppppppppppppppppppppppp548
Errata
An online log of corrections to Annual Review of Clinical Psychology articles may be
found at http://www.annualreviews.org/errata/clinpsy
viii Contents
Annu. Rev. Clin. Psychol. 2016.12:249-280. Downloaded from www.annualreviews.org
Access provided by Medical Research Council (UK) on 04/08/16. For personal use only.
... The visual mental imagery is related to various cognitive domains, such as attention, visual working memory, autobiographical episodic memory, and semantic memory (Aydin, 2018;Chica et al., 2014;Fulford et al., 2018;Keogh & Pearson, 2014;Pearson & Kosslyn, 2015). Previous studies have suggested that the change in mental imagery in depression patients mainly includes an excess of intrusive negative mental imagery, impoverished positive imagery, and overgeneral memory (i.e., difficulty in retrieving specific memories) (Anderson & Evans, 2015;Holmes et al., 2007Holmes et al., , 2008Holmes et al., , 2016Patel et al., 2007;Raes et al., 2006;Sumner et al., 2014). However, imagery exhibits complex cognitive changes in depression, and the neural mechanism underlying imagery cannot be explained by a single network or brain region. ...
... Past studies have found that visual mental imagery is impaired in depression (Weßlau et al., 2015;Williams & Moulds, 2007). People with depression are more likely to experience intrusive negative imagery, slow generation of imagery, and lack of detail in imagery (Holmes et al., 2016). Our study found similar results, with the MD group reported reduced vividness of visual mental imagery. ...
... In the MD group, the anterior fusiform gyrus exhibited negative connectivity with the ventral attention network, such as the insula. The decreased degree of the anterior fusiform gyrus is consistent with our hypothesis and may also be related to overgeneral semantic memory retrieval in depression (Holmes et al., 2016;Williams & Moulds, 2007;Haque et al., 2014). The negative emotions of depression will affect the retrieval of semantic information, language fluency, and constricting the scope of associations (Klumpp er al., 2010;Harel et al., 2022;Klumpp & Deldin, 2010). ...
Article
Full-text available
Background Impaired visual mental imagery is an important symptom of depression and has gradually become an intervention target for cognitive behavioral therapy. Methods Our study involved a total of 25 healthy controls (HC) and 23 individuals with moderate depressive symptoms (MD). This study explored the attentional mechanism supporting visual mental imagery impairments in depression using the Vividness of Visual Imagery Questionnaire (VVIQ), attentional network test (ANT), and resting-state functional magnetic resonance imaging (rs-fMRI). The intrinsic activity of attention-related regions relative to those supporting visual mental imagery was identified in depression patients. In addition, a meta-analysis was used to describe the cognitive function related to this intrinsic activity. Results The global correlation (GCOR) of the right anterior fusiform gyrus (FG) was decreased in depression patients. Attention-related areas were concentrated in the right posterior FG; the anterior and posterior functional connectivity (FC) of the FG was decreased in depression patients. Graph theoretic analysis showed that the degree of the right anterior FG was decreased, the degree of the anterior insula was increased, and the negative connection between these two regions was strengthened in depression patients. In addition, the degree of the right anterior FG, the FC between the subregions of the right FG, and the FC between the right anterior FG and insula were correlated with VVIQ scores; however, this correlation was not significant in depression patients. The meta-analysis suggested that the changes in the anterior FG in depressed patients may stem from difficulties of semantic memory retrieval. Conclusion The changed intrinsic activity of subregions of the FG relative to the semantic memory retrieval may be associated with visual mental imagery impairments in depression.
... Specifically, they suggest that enhancing positive affect through generation of imagery of positive future events, along with reducing the emotional impact of negative imagery, may be a promising mechanism to reduce not only negative affect but also anhedonia in depression [37]. Indeed, a growing body of literature shows that targeting distressing mental imagery using imagery re-scripting reduces depression in adults [4,43] and adolescents [33], and that increasing the vividness of positive future mental imagery reduces symptoms of anhedonia [3] and increases positive affect [15] in adults with depression. However, these treatment implications may be supported further by establishing a cross-time association between mental imagery variables and depressive symptoms. ...
... Our results indicate that targeting positive future mental imagery may be an important treatment target for reducing symptoms of anhedonia in adolescents, particularly as anhedonia is predictive of poorer clinical outcomes (Pizzagalli, 2022) and increased suicidal ideation, even after depressive symptoms have been controlled for (Ducasse et al., 2018). Indeed, imagery-based treatments that increase the vividness of positive future images have been shown to increase positive affect and reduce anhedonia in depression within adult populations [3,14,15]. These treatments are thought to increase positive affect by increasing positive imagery bias [3,15] and increasing anticipatory pleasure [14]. ...
... Indeed, imagery-based treatments that increase the vividness of positive future images have been shown to increase positive affect and reduce anhedonia in depression within adult populations [3,14,15]. These treatments are thought to increase positive affect by increasing positive imagery bias [3,15] and increasing anticipatory pleasure [14]. Future research should investigate whether these results can be replicated in depressed adolescent populations, but potentially in other mental health problems where anhedonia is present, such as schizophrenia [31] and eating disorders [9]. ...
Article
Full-text available
Adolescent depression is associated with unhelpful emotional mental imagery. Here, we investigated whether vividness of negative and positive prospective mental imagery predict negative affect and anhedonia in adolescents. 111 people from Israel completed measures of prospective mental imagery, negative affect, and anhedonia at two time-points approximately three months apart. Using three cross-lagged panel models, we showed once ‘concurrent’ (across-variable, within-time) and ‘stability’ paths (across-time, within-variable) were estimated, there were no significant cross-lag paths between: i) T1 prospective negative mental imagery and T8 negative affect (i.e. increased vividness of negative future imagery at Time 1 did not predict increased negative affect at Time 8); ii) T1 prospective positive mental imagery and T8 negative affect (i.e. reduced vividness of positive future imagery at Time 1 did not predict increased negative affect at Time 8); and iii) T1 prospective positive mental imagery and T8 anhedonia (i.e. reduced vividness of positive future imagery at Time 1 did not predict increased anhedonia at Time 8). Given high levels of attrition, future research should aim to explore these associations in a larger, more diverse population, as such data could inform on whether modifying earlier prospective mental imagery may influence later time/context-specific effects of prospective mental imagery on negative affect and anhedonia.
... Mental imagery depicts quasi-perceptual experiences that resemble perceptual experiences (Holmes et al., 2016;Thomas, 2019). It has been widely discussed in consumption behavior, but its application in the hotel context, not to mention the luxury hotels context, is scarce (Ha et al., 2019;Lv et al., 2020;Mou et al., 2019). ...
... Examples of such images in daily life include daydreaming and the mental visualization that occurs while reading a book. This ubiquitous mental event enables people to re-experience the past or to envision the future (Holmes et al., 2016). ...
... Particularly in clinical psychology, a growing body of research was able to demonstrate the positive relationship between mental imagery and positive affect (for a review see Holmes et al., 2016). Clinical psychologists assume that mental imagery, especially in the form of vividly imagining personal future events, boosts positive affect (for a recent meta-analysis, see Schubert et al., 2020). ...
... In a third phase, participants in both conditions received an imagery exercise during which they imagined a lemon using all their senses to familiarize them with mental imagery (Holmes et al., 2016). In a fourth phase, participants in the vision condition performed a guided visualization. ...
Article
Full-text available
In a rapidly changing world, leaders are constantly searching for effective ways to motivate employees and drive change. Management scholars agree that an essential tool for inspiring and motivating employees is to communicate a clear vision of the future. Yet, there remains a significant gap in understanding how and why visions actually move individuals to action. The current study investigated the effects of visions on goal-pursuit in comparison to merely listing a “superordinate goal.” We argue that visions, that are high in mental imagery, are motivationally effective because (a) visions evoke positive affect, (b) vision-evoked positive affect spills over to goals derived from the vision, leading to affectively charged goals, (c) affectively charged goals are predictive of increased commitment, and (d) increased commitment contributes to goal progress. In a first experimental study (N = 128), the findings suggest that visions and vision-derived goals were both higher in positive affect than our control condition. In a second experimental study (N = 323), we replicated our results from Study 1. In addition, we extended these findings and showed that visions predict goal progress via vision-evoked positive affect, positive anticipatory affect related to prospective vision-derived goal attainment, and goal commitment. Taken together, our studies contribute to research on visions and goals by showing that visions exert their motivational effects by affectively charging activities related to them. From a practical perspective, our studies highlight the importance of visions as an effective tool in motivating work-related behaviors.
... Similar depictions have been categorised as coping imagery in Berna et al. (2011Berna et al. ( , 2012. However, far from being positive, the image entailed self-harming behaviour that closely resembled thoughts of suicidal ideation in depression, as seen in Holmes et al. (2016). This may suggest that the outcomes associated with pain-related visual imagery may be akin to those found in mental health conditions. ...
Article
Full-text available
Chronic pain is common and debilitating, and recommended treatments are only moderately effective for pain relief. Focus has shifted to refining targets for change within psychological therapy to improve pain management. Evidence has shown the role of intrusive images in many psychological disorders. However, only a few studies have advanced our knowledge of the presence and impact of mental imagery in chronic pain. This exploratory study aimed to increase our understanding of how people with chronic pain perceive intrusive visual images to influence their daily life. The study employed a qualitative design, using semi-structured interviews to explore the content, emotional valence, cognitive and behavioural impact of pain-related visual images of ten participants with self-reported diagnosis of chronic pain. Data analysis was conducted by performing an inductive thematic analysis. Three key themes were identified: (1) ‘I start to create images in my head’: pain-related mental images, which revolves around descriptions of participants’ most significant visual image; (2) metaphors for pain, related to the imagery as a means to conceptualise and give meaning to the pain; and (3) “With the pain comes the image”: a companion to pain, which focuses on the role of intrusive images in the experience of pain. Results show that pain-related mental imagery appeared to be an intrusive, uncontrollable, and vivid cognitive accompaniment for many pain sufferers. The findings suggest that mental images may serve as an additional target in cognitive behavioural therapy to enhance individuals’ cognitive, behavioural and emotional change. Key learning aims (1) To understand the role of mental imagery in the daily life of individuals with chronic pain. (2) To examine the impact of intrusive images on the emotions, cognitions, and behaviours of people with chronic pain. (3) To consider clinical implications for CBT interventions targeting pain-related mental images to manage chronic pain.
... Research suggests that off-task thoughts and imagination may activate similar brain regions (Villena-Gonzalez & Cosmelli, 2020). Moreover, the ability to guide imaginative thoughts has been linked with a greater likelihood of generating positive emotional outcomes (Holmes et al., 2016). This positive tendency is usually more evident in self-directed, unrestricted thought, where imagination is an actively engaged component. ...
Article
Full-text available
William James’ “stream of thought” is a key component of human cognition. Such thoughts arise in both restricted and unrestricted contexts, either with or without the presence of a secondary task. This study examines the similarities and differences in thoughts produced in these two contexts, which we call restricted and unrestricted mind wandering. Participants performed a mindfulness task representing restricted mind wandering and an unrestricted thought task where they spontaneously explored thoughts, reporting them as they arose. Participants then self-rated their thoughts based on valence, temporal orientation (past/present/future), and reality orientation (imaginary vs. real). Participants’ emotional states were also evaluated using the Emotion Recall Task (ERT) and the PANAS questionnaire. Unrestricted mind wandering generated more thoughts, which were more positive and future-oriented than those in restricted mind wandering. Additionally, participants’ thought valence correlated with their PANAS and ERT scores. Approximately 1 out of 4 thoughts in both restricted and unrestricted mind wandering were imaginary, with increased future orientation linked to more imaginative thought. Despite the statistical differences separating restricted and unrestricted thought, effect sizes were predominantly small, indicating that the thoughts arise during these two types of mind wandering are largely of the same kind.
... Mental imagery is the overt basis of human cognitive abilities [1]. Motor imagery (MI) is one of the most common imagery cognitive processes, in which subjects only need to perform the imagination of motor action (e.g., left-or right-hand movement) without any execution [2]. ...
Article
Full-text available
Complementary to brain–computer interface (BCI) based on motor imagery (MI) task, sensory imagery (SI) task provides a way for BCI construction using brain activity from somatosensory cortex. The underlying neurophysiological correlation between SI and MI was unclear and difficult to measure through behavior recording. In this study, we investigated the underlying neurodynamic of motor/tactile imagery and tactile sensation tasks through a high-density electroencephalogram (EEG) recording, and EEG source imaging was used to systematically explore the cortical activation differences and correlations between the tasks. In the experiment, participants were instructed to perform the left and right hand tasks in MI paradigm, sensory stimulation (SS) paradigm and SI paradigm. The statistical results demonstrated that the imagined MI and SI tasks differed from each other within ipsilateral sensorimotor scouts, frontal and right temporal areas in α bands, whereas real SS and imagined SI showed a similar activation pattern. The similarity between SS and SI may provide a way to train the BCI system, while the difference between MI and SI may provide a way to integrate the discriminative information between them to enhance BCI performance. The combination of the tasks and its underlying neurodynamic would provide a new approach for BCI designation for a wider application. BCI studies concentrate on the hybrid decoding method combining MI or SI with SS, but the underlining neurophysiological correlates between them were unclear. MI and SI differed from each other within the ipsilateral sensorimotor cortex in alpha bands. This is a first study to investigate the neurophysiological relationship between MI and SI through an EEG source imaging approach from high-density EEG recording.
... We therefore conjecture that VR-P, as a perceptual experience rather than one that involves visual mental imagery, may serve as an equalizer of the experience of high vividness across individuals. As a result, VR-P may be particularly helpful to groups of persons who tend to score lower in trait vividness of positive EC-I and so may be compromised in their positive response to EC-I, such as depressed persons (e.g., Holmes et al., 2016). Moreover, negative affective responses were rarely reported at any level of intensity to VR-P (or EC-I) in the present study, even among those who reported greater depression and anxiety at baseline using a screening questionnaire. ...
Article
Full-text available
Virtual reality (VR) has shown promise as a psychological means of inducing mystical experiences. Here, we compared the subjective responses of 48 undergraduate volunteers to script-guided multiuser perceptual experiences in VR (VR perception [VR-P]) with their responses to a control condition involving guided imagery while their eyes were closed (eyes-closed imagery). Nineteen participants (40%) met the criteria for a “complete” mystical experience in response to VR-P on the Mystical Experiences Questionnaire–30 (MEQ-30), while only three (5%) achieved this in response to eyes-closed imagery. VR-P was also more evocative of a sense of presence, vividness, and absorption, as well as various positive affective experiences, most prominent among which included awe, beauty, and being mindfully observant, but also novelty, interest, contentment, and joy. Comparably, negative affective responses were rarely reported even at a very low intensity. Guided perception in VR of a beautiful, realistic environment also inclusive of awe-provocative, surrealistic elements thus could be an effective method to induce mystical experiences in at least a sizable minority of participants.
Article
The ability to focus on and increase positive emotion in response to mental imagery may play a key role in emotional wellbeing. Moreover, deficits in this ability might underlie emotional disorders such as depression. Here, we set out to determine whether people could use savoring to upregulate subjective and electrocortical response to mental imagery of previously viewed positive and neutral pictures, and whether this would be negatively affected by depression. On each trial, participants (N = 49) viewed a positive or neutral picture, prior to simply re-imagining the previously presented picture (“view”) or re-imagining the picture while savoring it (“savor”). Results showed that savoring increased electrocortical and subjective response to imagined stimuli; however, this effect was only evident at the electrocortical level when controlling for depression. Moreover, depression moderated electrocortical findings, such that individuals who were more depressed showed a reduced effect of savoring on neural response to mental imagery. Results are in line with recent work that has shown the benefits of positive affect treatment for depression, to suggest that deficits in savoring mental imagery may play a role in the development and/or maintenance of depression.
Chapter
In the last two decades, an approach to the study of motivation has emerged that focuses on specific cognitive and affective mediators of behaviour, in contrast to more general traits or motives. This 'social-cognitive' approach grants goal-oriented motivation its own role in shaping cognition, emotion and behaviour, rather than reducing goal-directed behaviour to cold-blooded information processing or to an enactment of a personality type. This book adds to this process-oriented approach a developmental perspective. Critical elements of motivational systems can be specified and their inter-relations understood by charting the origins and the developmental course of motivational processes. Moreover, a process-oriented approach helps to identify critical transitions and effective developmental interventions. The chapters in this book cover various age groups throughout the life span and stem from four big traditions in motivational psychology: achievement motivation, action theory, the psychology of causal attribution and perceived control, and the psychology of personal causation and intrinsic motivation.
Article
Over the past 25 years the pace of progress in neuroscience research has been extraordinary, with advances in both understanding and technology. We might expect that this would stimulate improved understanding and treatment of mental health problems, yet in general this has not been the case. In fact, our standard treatment approaches have barely changed in decades, and still fail many people suffering from mental distress. Why is there this disconnect between knowledge and application? And could we be on the brink of an exciting new era of cooperation between the two disciplines, increasing the effectiveness of existing treatments and even suggesting new ones?
Article
Aims: Studies have shown that gambling is associated with poor health and health risk-taking behaviour. However, little is known about those factors that can influence the association between gambling, health risk-taking and health. Using a population-based School Health Promotion Study of eighth- and ninth-grade Finnish boys and girls (N = 62,956), we investigated the relationships between gambling frequency, health risk-taking and poor health as well as whether social support from parents, friends and school staff could mediate these associations. Methods: Path analysis was used to discover direct and indirect effects of health, health risk-taking and gambling. Results: Social support from parents and school staff decreased gambling among boys and girls, whereas among boys support from friends increased gambling. However, the role of social support as a mediator was very weak. Overall poor health and health risk-taking were associated with increased gambling. CONCLUSIONS GAMBLING SHOULD BE CONSIDERED AN IMPORTANT PUBLIC HEALTH ISSUE BECAUSE IT CLUSTERS WITH OTHER UNHEALTHY BEHAVIOUR PATTERNS INTERVENTIONS CONCERNING ADOLESCENT GAMBLING SHOULD ALSO TAKE OTHER SIMULTANEOUS RISK-TAKING INTO CONSIDERATION ALSO SOCIAL SUPPORT FROM PARENTS AND SCHOOL SHOULD BE NOTED WHEN TRYING TO DECREASE ADOLESCENTS' GAMBLING.
Article
Background and objectives: Social stress and associated coping responses can profoundly influence women's stress physiology and health. Implicit social attentional biases can also influence psychological and physiological stress responses. The purpose of this study was to explore whether a coping style characterized by greater use of social support predicts indices of cortisol activity in laboratory and daily life contexts among female university students. We hypothesized that the relation of this coping style to cortisol activity would be moderated by women's attentional biases. Methods: Seventy-four women (Mage = 19.44, range: 17.8-27.8, 64% White) completed an interpersonal stress task and an attentional bias task in the lab, along with a self-report coping inventory. Participants provided five saliva samples during the lab protocol, followed by three saliva samples per day for three consecutive weekdays. Outcome measures included cortisol response to lab tasks (AUCg), diurnal cortisol slope, diurnal AUCg, and cortisol awakening response (CARi). Results: A coping style characterized by greater use of social support predicted lower lab AUCg and lower, flatter average diurnal cortisol slope for women with attentional avoidance compared to women with attentional vigilance (ps < .05). Conclusions: Responding to stress by using social support is linked to lower cortisol responses to social stress and diurnal cortisol activity for women with implicit avoidance of social threat cues.
Article
People with emotional disorders, such as social anxiety disorder (SAD), generalized anxiety disorder (GAD), and depression, demonstrate a consistent tendency, or bias, to generate negative interpretations of ambiguous material. This is different from people without emotional disorders who tend, in general, to make positive interpretations of ambiguity. If central components of an emotional disorder have high levels of inherent ambiguity (e.g., concern about the negative perceptions of others in SAD, or worry in GAD), then interpretive bias may have a causal maintaining role, and this has been demonstrated in studies using cognitive bias modification techniques. This research has also shown that interpretation biases combine with other cognitive processes, such as imagery and memory, which could exacerbate distress. Psychological interventions will benefit from effectively targeting negative interpretations, and future experimental research can inform ways to improve facilitation of more benign inferential processing to maximize amelioration of key components of emotional disorders.