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Systematic Review of Occupational Therapy and Adult Cancer Rehabilitation: Part 1. Impact of Physical Activity and Symptom Management Interventions

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This article is the first part of a systematic review of evidence for the effectiveness of cancer rehabilitation interventions within the scope of occupational therapy that address the activity and participation needs of adult cancer survivors. This article focuses on the importance of physical activity and symptom management. Strong evidence supports the use of exercise for cancer-related fatigue and indicates that lymphedema is not exacerbated by exercise. Moderate evidence supports the use of yoga to relieve anxiety and depression and indicates that exercise as a whole may contribute to a return to precancer levels of sexual activity. The results of this review support inclusion of occupational therapy in cancer rehabilitation and reveal a significant need for more research to explore ways occupational therapy can positively influence the outcomes of cancer survivors. Part 2 of the review also appears in this issue. © 2017, American Occupational Therapy Association, Inc. All rights reserved.
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CENTENNIAL TOPICS
Systematic Review of Occupational Therapy and Adult
Cancer Rehabilitation: Part 1. Impact of Physical Activity
and Symptom Management Interventions
Elizabeth G. Hunter, Robert W. Gibson, Marian Arbesman,
Mariana D’Amico
Elizabeth G. Hunter, PhD, OTR/L, is Assistant
Professor, Graduate Center for Gerontology, University of
Kentucky, Lexington; eghunt2@uky.edu
Robert W. Gibson, PhD, MS, OTR/L, FAOTA, is
Professor and Director of Research, Department of
Emergency Medicine, Medical College of Georgia,
Augusta University, Augusta, GA.
Marian Arbesman, PhD, OTR/L, FAOTA, is
Consultant, Evidence-Based Practice Project, American
Occupational Therapy Association, Bethesda, MD;
President, ArbesIdeas, Inc., Williamsville, NY; and Adjunct
Associate Professor, Department of Clinical Research and
Leadership, School of Medicine and Health Sciences,
George Washington University, Washington, DC.
Mariana D’Amico, EdD, OTR/L, BCP, FAOTA, is
Associate Professor, Department of Occupational Therapy,
Nova Southeastern University, Fort Lauderdale, FL.
This article is the first part of a systematic review of evidence for the effectiveness of cancer rehabilitation
interventions within the scope of occupational therapy that address the activity and participation needs of
adult cancer survivors. This article focuses on the importance of physical activity and symptom management.
Strong evidence supports the use of exercise for cancer-related fatigue and indicates that lymphedema is not
exacerbated by exercise. Moderate evidence supports the use of yoga to relieve anxiety and depression and
indicates that exercise as a whole may contribute to a return to precancer levels of sexual activity. The results
of this review support inclusion of occupational therapy in cancer rehabilitation and reveal a significant need
for more research to explore ways occupational therapy can positively influence the outcomes of cancer
survivors. Part 2 of the review also appears in this issue.
Hunter, E. G., Gibson, R. W., Arbesman, M., & D’Amico, M. (2017). Centennial Topics—Systematic review of occupational
therapy and adult cancer rehabilitation: Part 1. Impact of physical activity and symptom management interventions.
American Journal of Occupational Therapy, 71, 7102100030. https://doi.org/10.5014/ajot.2017.023564
Cancer may result in impairments, activity limitations, and participation
restrictions (Fialka-Moser, Crevenna, Korpan, & Quittan, 2003; Grov, Fossa
˚,
& Dahl, 2010; Hewitt, Rowland, & Yancik, 2003; Hwang, Lokietz, Lozano, &
Parke, 2015). Cancer survivorship covers the time from diagnosis until the end of life
(National Cancer Institute, 2015). Cancer survivors may have declines in func-
tioning and participation in areas ranging from mobility to return to work (Hwang
et al., 2015; Kroenke et al., 2004; Nomori, Watanabe, Ohtsuka, Naruke, &
Suemasu, 2004). Adults with cancer experience decreased levels of physical func-
tioning and participation in social, work, and leisure activities compared with before
diagnosis regardless of the kind of cancer or type of treatment received (Ganz et al.,
2004; Grov et al., 2010). The lowest function is experienced after treatment, with
function increasing over time, although functional recovery is moderated by pain
and co-occurring diseases (Hwang et al., 2015; Ko, Maggard, & Livingston, 2003).
The Institute of Medicine and National Research Council have strongly
suggested that cancer survivor research should include expanded exploration of
alternative models of survivorship care, such as supportive care and rehabilitation
Note. Each issue of the 2017 volume of the American Journal of Occupational Therapy features a special Centennial
Topics section containing several articles related to a specific theme; for this issue, the theme is occupational
therapy’s role in cancer treatment and recovery. The goal is to help occupational therapy professionals take stock
of how far the profession has come and spark interest in the many exciting paths for the future. For more information,
see the editorial in the January/February issue, https://doi.org/10.1054/ajot.2017.711004.
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programs (Hewitt, Greenfield, & Stovall, 2006; Institute of
Medicine, 2013). However, a major problem in the U.S.
health care system is that cancer survivors are frequently not
referred for and do not receive specialized rehabilitation care
appropriate for their diagnosis (Cheville, Troxel, Basford, &
Kornblith, 2008; Pergolotti, Cutchin, Weinberger, & Meyer,
2014). Rehabilitation is the standard of care for conditions
such as heart disease or stroke but, unfortunately, not for
cancer and cancer survivorship (Cheville et al., 2008; Segal
et al., 1999).
Cancer rehabilitation can benefit people with cancer
from diagnosis to end-of-life care. The goals of cancer
rehabilitation might focus on symptom management or
helping a survivor return to work or community partic-
ipation (Gamble, Gerber, Spill, & Paul, 2011). The role
of occupational therapy practitioners is well suited to
helping cancer survivors at all stages of illness.
Objective of the Systematic Review
The objective of the cancer rehabilitation review was to
systematically search for and assess interventions within the
scope of occupational therapy practice to improve occupa-
tional engagement. The focused question guiding selection
of research studies for review was “What is the effectiveness
of cancer rehabilitation interventions within the scope of
occupational therapy practice to address the activity and
participation needs of adult cancer survivors in activities of
daily living, instrumental activities of daily living, work,
leisure, social participation, and rest and sleep?”
This systematic review was supported by the American
Occupational Therapy Association (AOTA) as part of the
Evidence-Based Practice (EBP) Project (Lieberman & Scheer,
2002). Because of the breadth of the systematic review, the
results were divided into two parts. In this article, we report
on Part 1 of the systematic review, which is focused on the
importance of physical activity and symptom management
for cancer survivors. Part 2, also in this issue, is focused on
multidisciplinary rehabilitation and interventions that address
psychosocial outcomes, sexuality, and return to work.
Method
Process
The research question and search terms for the reviews
were developed by the methodology consultant, AOTA staff,
and the advisory group in consultation with the review au-
thors. The search terms were related to population (adult
cancer survivors), types of intervention, outcomes, sequelae,
and types of study design to be included in the systematic
review. A medical research librarian with experience in
completing systematic review searches conducted all
searches and confirmed and improved the search strategies.
Databases and sites searched included Medline, PsycINFO,
CINAHL, and OTseeker. In addition, consolidated in-
formation sources, such as the Cochrane Database of Systematic
Reviews, were included in the search. Reference lists from
articles included in the systematic reviews were examined for
potential articles, and selected journals were hand searched to
ensure that all appropriate articles were included.
Inclusion Criteria
Included in the review were peer-reviewed scientific ar-
ticles on adults with cancer published in English between
1995 and 2014 and within the scope of practice of occu-
pational therapy. The review excluded data from presenta-
tions, conference proceedings, non–peer-reviewed research
literature, dissertations, and theses. The review also excluded
studies focusing on caregivers, family members, or friends
rather than cancer survivors; studies of childhood cancer; and
interventions that required an academic degree other than
occupational therapy (e.g., music therapy, neuropsychology).
AOTA uses standards of evidence modeled on those devel-
oped in evidence-based medicine (Lieberman & Scheer, 2002;
Sackett, Rosenberg, Gray, Haynes, & Richardson, 1996):
Level I: Systematic reviews, meta-analyses, randomized
controlled trials (RCTs)
Level II: Two-group, nonrandomized studies (e.g., co-
hort, case control)
Level III: One-group, nonrandomized studies (e.g.,
pretest and posttest)
Level IV: Descriptive studies that include analysis of
outcomes (e.g., single-subject design, case series)
Level V: Case reports and expert opinion that include
narrative literature reviews and consensus statements.
Studies included in the review provide Level I, II, and III
evidence. Level IV and V evidence was excluded from this
part of the review.
Data Extraction
The team of three reviewers (Hunter, Gibson, D’Amico)
worked together to evaluate all articles at all stages of the
review. Eligibility assessment was performed independently
in an unblended, standardized manner by the three
reviewers. Disagreements among reviewers were resolved
by consensus. The synthesis entailed a detailed reading of
the studies and completion of an evidence table describing
each study specifically. Figure 1 depicts the flow of abstracts
and articles through the process, and the evidence table
is provided in Supplemental Table 1 (available online at
http://ajot.aotapress.net; navigate to this article, and click on
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“Supplemental Materials”). The articles were grouped into
themes and analyzed and reported by theme.
Analysis
AOTA staff and the EBP Project consultant reviewed the
evidence tables to ensure quality control. Analysis of study
design, outcomes, and risk of bias determined which studies
were assessed as strong or moderate evidence. Strong evi-
dence typically includes 2 or more well-designed RCTs.
Moderate evidence includes 1 RCT, 2 or more studies
providing lower level evidence, or inconsistent findings from
well-designed projects. Only selected articles from the sys-
tematic review are mentioned in this article.
Results
The review team identified 138 articles for inclusion in the
final qualitative synthesis; 86 articles are included in this
Figure 1. Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) flow diagram of physical activity and symptom
management studies included in the systematic review.
Note. PAMs 5physical agent modalities. Format from “Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement,” by
D. Moher, A. Liberati, J. Tetzlaff, and D. G. Altman; The PRISMA Group, 2009, PloS Medicine, 6(6): e1000097. https://doi.org/10.1371/journal.pmed.1000097
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article (Part 1). The remainder are discussed in Part 2. The
articles provide Level I evidence, with the exception of 1 Level
III article. Articles were organized into two broad intervention
areas: (1) physical activity interventions, including exercise (25
articles) and complementary and alternative medicine
(CAM; 26 articles), and (2) symptom management in-
terventions, including pain, fatigue, and breathlessness (19
articles); lymphedema (12 articles); and physical agent
modalities (PAMs; 4 articles). Details about each article are
giveninSupplementalTable1(online).
Risk of Bias
The risk of bias of individual studies was assessed using
the Cochrane risk-of-bias guidelines described by Higgins,
Altman, and Sterne (2011; see Supplemental Table 2,
online). The method for assessing the risk of bias of
systematic reviews was based on the Assessment of Mul-
tiple Systematic Reviews (AMSTAR) system developed
by Shea et al. (2007; see Supplemental Table 3, online).
Physical Activity Interventions
Twenty-five Level I articles related to exercise met the
criteria for the review; 11 were systematic reviews and 14
were RCTs. Twenty-six Level I articles related to com-
plementary and alternative medicine met the criteria and
were included in the review; 21 were systematic reviews
and 5 were RCTs. CAM physical activity interventions
included yoga, Qigong, Tai Chi, and dance.
Strong Evidence. Strong evidence was found that ex-
ercise is safe and beneficial for the majority of cancer types,
at all stages including end of life, and regardless of age
(Adamsen et al., 2009; Albrecht & Taylor, 2012; Baumann,
Zopf, & Bloch, 2012; Beaton et al., 2009; Daley et al.,
2007; Henke et al., 2014; Hwang et al., 2008; Spence,
Heesch, & Brown, 2010). Exercise, particularly aerobic
exercise, reduced cancer-related fatigue (CRF; Andersen
et al., 2013; Kuchinski, Reading, & Lash, 2009; McMillan
& Newhouse, 2011; McNeely et al., 2006). Exercise
also increased muscle tone and strength and lung capacity
(Granger, McDonald, Berney, Chao, & Denehy, 2011;
Keogh & MacLeod, 2012). Exercise was found not to
cause lymphedema or to make existing lymphedema
worse (Cormie et al., 2013; McClure, McClure, Day, &
Brufsky, 2010).
Moderate Evidence. Moderate evidence was found that
exercise improves health-related quality of life (HRQOL)
for some survivors. Rehabilitation using physical training
(strength, interval, and home-based activities) was signifi-
cantly better than usual care in terms of HRQOL (Basen-
Engquist et al., 2006; Beaton et al., 2009; Korstjens et al.,
2008). Supervised exercise was better than nonsupervised
exercise (Knols, de Bruin, Shirato, Uebelhart, & Aaronson,
2010), and counseling and telephone support were helpful
in keeping people exercising (Knols et al., 2010). Diet and
exercise interventions reduced the rate of self-reported
functional decline (Morey et al., 2009; Rogers et al., 2009).
Exercise improved sleep quality for people undergoing
cancer treatment (Sprod et al., 2010; Tang, Liou, & Lin,
2010).
Moderate evidence was found that yoga, regardless
of type, benefits mental health, quality of life, sleep, and
sense of well-being and decreases stress (Cramer, Lange,
Klose, Paul, & Dobos, 2012; Harder, Parlour, & Jenkins,
2012; Mustian et al., 2013; Shneerson, Taskila, Gale,
Greenfield, & Chen, 2013). Qigong improved quality of
life, mood, fatigue, and immune response and reduced
inflammation (Chan et al., 2012; Oh et al., 2012; Zeng,
Luo, Xie, Huang, & Cheng, 2014).
Symptom Management Interventions
Nineteen articles addressing pain, fatigue, and breath-
lessness in cancer patients and survivors met the criteria for
the review; 5 were systematic reviews, and 14 were RCTs.
Twelve articles related to lymphedema treatment; 6 were
systematic reviews, 5 were RCTs, and 1 was a Level III
study. Finally, 4 articles related to the use of PAMs to treat
lymphedema met the criteria for the review; 1 was a
systematic review, and 3 were RCTs.
Strong Evidence. Strong evidence was found that ex-
ercise reduces CRF and increases quality of life (Kuchinski
et al., 2009; Wanchai, Armer, & Stewart, 2011). Non-
pharmacological interventions, such as problem solving,
energy conservation, and education, reduced the symptom
of breathlessness (Corner, Plant, A’Hern, & Bailey, 1996;
Zhao & Yates, 2008). The use of neuromuscular electrical
stimulation in conjunction with traditional swallowing
training facilitated greater recovery than swallowing training
alone for adults after head and neck cancer treatment (Ryu
et al., 2009).
Regarding lymphedema management, compression
bandages worn on a daily basis were found to be important
for volume control (Devoogdt, Van Kampen, Geraerts,
Coremans, & Christiaens, 2010; Kim & Park, 2008;
King, Deveaux, White, & Rayson, 2012; Preston, Seers,
& Mortimer, 2004). Exercise was found not to make
lymphedema worse and to improve mood, quality of life,
range of motion, and weight loss (Kim, Sim, Jeong, &
Kim, 2010; McClure et al., 2010).
Moderate Evidence. Moderate evidence was found sup-
porting sleep therapy modifications, education and problem
solving for pain management, and cognitive–behavioral ther-
apy in CRF management (Armes, Chalder, Addington-Hall,
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Richardson, & Hotopf, 2007; Berger et al., 2009; Gielissen,
Verhagen, Witjes, & Bleijenberg, 2006; Jacobsen, Donovan,
Vadaparampil, & Small, 2007; Ling, Lui, & So, 2012;
Oldenmenger, Sillevis Smitt, van Montfort, de Raaf, &
van der Rijt, 2011). Moderate evidence also supports the
use of PAMs, including low-frequency, low-intensity
electrotherapy to reduce feelings of pain, heaviness, and
tightness when treating lymphedema of the arm (Belmonte
et al., 2012).
Discussion
Part 1 of the systematic review provides evidence that
physical activity is helpful for people diagnosed with
cancer. The type of physical activity in these studies
was varied and included aerobic, light and heavy re-
sistance, walking activities, aquatic exercise, yoga, Qigong,
and Tai Chi, among others. Occupational therapy prac-
titioners can help clients incorporate physical activity into
their daily routines to enhance health, wellness, and
quality of life. Physical activity can help reduce CRF,
improve the quality of sleep, increase physical function,
and increase HRQOL regardless of type or stage of cancer.
It is beneficial for some clients pretreatment and for most
clients during and after treatment (Spence et al., 2010).
Strong evidence indicates that exercise, including
resistance, aerobic, or a combination of the two, does not
exacerbate lymphedema and provides other physical and
mental health benefits. Moderate evidence exists for the
use of CAM; the strength of this evidence is negatively
affected by the quality of the studies and high risk of bias.
Moderate evidence supports the use of the CAM interventions
of yoga, Qigong, and mindfulness-based interventions to
improve quality of life and mental health outcomes.
Symptom management is another area in which oc-
cupational therapy intervention is useful. The most com-
mon symptoms assessed in the literature were pain, fatigue,
and breathlessness. Occupational therapy practitioners
should include exercise and other physical activity and
occupation-based interventions such as problem solving,
energy conservation, and education to address these symp-
toms. Cognitive–behavioral therapy and psychoeducational
programming also can be useful in treating CRF. Ad-
ditionally, occupational therapy practitioners can feel
confident in suggesting physical activity to clients with
lymphedema.
Many studies were found that addressed treatment of
lymphedema, but the majority did not qualify for this
review because they addressed only arm volume and not
functional outcomes. The studies included in the review
show strong support for the use of compression bandages
to improve functional outcomes, particularly when com-
bined with therapy that includes skin care, range of motion,
and strengthening.
Overall, the evidence indicates that use of PAMs can
be beneficial in treating lymphedema for some people
diagnosed with cancer. PAMs can improve the pain
that accompanies lymphedema, along with the feelings
of heaviness and tightness. Currently, no evidence indicates
that transcutaneous electrical nerve stimulation improves
chronic pain among cancer survivors.
Three major gaps exist in the research examining
cancer rehabilitation interventions. First, more high-
quality, rigorous study designs are needed to provide the
best, most reliable results. Second, most studies were not
specific about the use of or return to meaningful activities
and participation for either assessments or outcomes.
Third, only a handful of the studies examined occupation-
based interventions. As occupational therapy practitioners
develop and take part in high-quality studies in the area of
cancer rehabilitation, they should ensure that these studies
include outcomes that go beyond physical function to
address activity and participation.
Implications for Occupational
Therapy Practice
Most studies in this review are within the scope of
occupational therapy practice but lack a focus on im-
portant outcomes of function and participation. This
evidence should be viewed as indicating initial steps to-
ward achieving functional outcomes and not achievement
of the outcomes themselves. Occupational therapy prac-
titioners must interpret and apply this evidence within
their unique professional understanding of function, en-
gagement, and participation.
Occupational therapy practitioners can use a wellness
or health promotion approach to encourage meaningful
activity and exercise. AOTA (n.d.) has called on prac-
titioners to help people prevent and manage chronic
disease through a health and wellness model. Practi-
tioners can feel confident in incorporating physical ac-
tivity into their practice because strong evidence indicates
that exercise helps in multiple ways (e.g., mental health,
physical health, symptom management) and does not make
symptoms worse (i.e., lymphedema, fatigue). Exercise is
clearly beneficial, but it does not have to consist of lifting
weights at the gym; yoga and Qigong were found to be
beneficial as well. Physical activity is helpful for maintaining
weight, increasing muscle strength, improving sleep, and
reducing cancer-related fatigue (CRF), among other positive
outcomes.
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Occupational therapy practitioners are well suited to
conduct individual and group yoga, Qigong, and mind-
fulness interventions to improve symptom management,
mental health, quality of life, participation in daily living
occupations, and social engagement. These are important
factors for cancer survivors and are not always addressed as
fully as they could be. Practitioners need to keep in mind
that cancer survivorship symptom management is far more
than lymphedema care. Although this is the symptom
rehabilitation professionals have focused on most fully,
CRF, pain, sleep disorders, and breathlessness are more
common and less often addressed.
Implications for Research
More rigorous, better designed research is needed to provide
a greater understanding of which people need what type of
intervention at what point in their cancer care and survi-
vorship. Specifically, more research is needed that focuses on
participation outcomes and occupation-based interventions.
The area of exercise is the best researched and has the
most robust outcomes in terms of cancer survivorship and
cancer rehabilitation, but the occupational therapy focus
of participation and occupation is missing in this research.
Most of the exercise studies looked at the use of traditional
exercise as an intervention; the occupational therapy point
of view might provide a richer understanding of how to in-
corporate the broader idea of physical activity into a client’s life.
In terms of symptom management, most interventions
were not conducted by occupational therapy practitioners.
The vast majority were conducted by nurses, social workers,
or psychologists. Occupational therapy–specific studies are
needed that look at return to participation and occupation-
based interventions as they relate to managing symptoms in
cancer survivors. In general, few of the studies moved into
the realm of occupation, particularly in terms of outcomes.
Occupational therapy researchers could make strong con-
tributions toward filling this gap in research.
Limitations
Limitations of the systematic review result from limitations
in the individual studies’ designs and methods, including
small sample sizes, short intervention periods, limited use of
standardized assessment, and short follow-up periods. Many
studies included multiple interventions, so pinpointing the
effects of any single intervention may not be possible. Fi-
nally, the role of occupational therapy in the multidisci-
plinary interventions was seldom discussed. Many studies
focused on impairment interventions and the outcomes of
symptom management and quality of life rather than the
occupational therapy’s concern with function, occupational
engagement, performance, and social participation.
Conclusion
Occupational therapy practitioners working with survivors
of cancer of all types, stages, and points on the survivorship
continuum have a body of evidence to support current
and future practice. More research is needed to support
occupation-based interventions geared toward positive
activity and participation outcomes for this large and
continually growing population. s
Acknowledgments
We thank Deborah Lieberman, Program Director, AOTA
Evidence-Based Practice Project, for her guidance and
support during the process of this review. Marian Arbesman
is Methodology Consultant, AOTA Evidence-Based Practice
Project; no other potential conflicts of interest are reported.
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The American Journal of Occupational Therapy 7102100030p11
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... In a recent systematic review on physical activity and symptom management interventions in cancer, Hunter et al. [5] included 138 studies of occupational therapy intervention, many of which showed positive effects on quality of life and chronic disease symptom management. However, the vast majority of included studies did not actually involve interventions delivered by an occupational therapist, and few studies included outcome measures that explicitly capture occupational performance or activities of daily living. ...
... At the same time, the review demonstrates the preoccupation with symptom control and motor function improvement that characterizes cancer rehabilitation research to date. Although the importance of these targets for cancer rehabilitation has not been disputed, we point out that general exercise interventions lack specificity for improving activities of daily living [5]. ...
... Further study is needed on occupational therapy as an intervention for patients who have supportive care needs that are clearly related to daily functioning. Meanwhile, more research is needed to explicitly evaluate the effectiveness of occupational therapy in improving daily activities and quality of life for cancer patients and survivors [5]. A systematic review and meta-analysis by Tofany et al. [6] studied the effectiveness of occupational therapy interventions in the quality of life of patients with Parkinson's disease. ...
Article
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Background: The purpose of this research is to study the effect of occupational therapy on the quality of life and pain self-efficacy among chronic disease patients. In this context, differences in quality of life and pain self-efficacy were investigated between patients who have followed occupational therapy and patients who have not followed the program of occupational therapy. Methods: The sample consists of 63 people, all chronic disease patients. Of the above patients, according to the research design, half received occupational therapy services at a rate of 50.8% (32 patients), while the remaining 49.2% (31 patients) did not receive them. For the data collection MVQOLI-15 and PSEQ were used. Results: We found that those receiving occupational therapy services, on average, seem to have comparatively better pain self-efficacy and overall quality of life compared to those not receiving them, while this difference is statistically significant, with the level of statistical significance amounting to α = 5%. Conclusion: The effect of occupational therapy on quality of life and pain self-efficacy in chronic disease patients is crucial.
... 16,17 Expanding high-level evidence 18 demonstrates that when provided to BCSs, cancer-specialized rehabilitation interventions can mitigate, [18][19][20][21] and may even prevent, 22 treatment-related impairments. Furthermore, evidence from systematic reviews 5,[23][24][25] and observational studies of cancer rehabilitation services delivered in the community 16,21,26,27 demonstrate that participation in these interventions is associated with improved HRQoL, including physical, mental, functional, and social domains. Taken together, this evidence suggests that rehabilitation interventions may enhance work ability by addressing HRQoL needs. ...
Article
Background: Breast cancer survivors (BCSs) report persistent, diminished ability to work, and decreased health-related quality of life (HRQoL). Cancer rehabilitation interventions (physical therapy or occupational therapy [PT/OT]) aim to improve these outcomes, but little is known about their impact in the community. Methods: This retrospective, pre-post, uncontrolled study examined cases of younger BCSs (age <65 years) who attended cancer-specialized PT/OT over a 2-year period. Outcomes and covariates (age, race, US region, payer type, number of visits, length of care [weeks]) were extracted from electronic medical records. Patient-reported outcomes were overall-Work Ability Score (WAS overall ), physical-WAS (WAS physical ), and mental-WAS (WAS mental ) and PROMIS Global Physical Health (GPH), Global Mental Health (GMH), Physical Function (PF), and Ability to Participate in Social Roles and Activities (SRA). We used linear mixed effect models to examine pre- to post-rehabilitation change overall, and separately, while controlling for covariates. Results: PT/OT cases (N PT =758; N OT =140) had a mean [SD] age of 51.39 [8.49] years and attended approximately 12 visits (IQR, 8.0–19.0) over 10.71 weeks (IQR, 6.14–17.00). Overall, work ability outcomes (WAS overall : +1.79; WAS physical : +0.78; WAS mental : +0.47; all P <.001) and HRQoL outcomes improved significantly (GPH: +5.38; GMH: +2.90; PF: +5.17; SRA: +5.83; all P <.001), and average change on each HRQoL outcome exceeded the minimal important change (2 points). Outcome scores were similar at each timepoint for both PT and OT cases (all P >.05) and both groups improved significantly (all P <.01). Conclusions: In this large study of the impact of cancer-specialized, community-based PT and OT, younger BCSs reported significant improvement in ability to work and HRQoL. Although more research is needed, these findings suggest improved access to PT/OT could improve work ability and HRQoL for younger BCSs.
... PT/OT are skilled services covered by most insurances with the goal of reducing the negative impact of treatment-related side effects on daily life, improving functional independence, participation in life roles, and HRQOL [24]. Meta-analyses of controlled research studies demonstrate the efficacy of PT/OT interventions in alleviating treatment-related side effects (pain, lymphedema, fibrosis, atrophy, etc.) and optimizing functional independence (ability to complete self-care, daily or social activities, return to work, etc.) [25][26][27][28]. In addition, growing evidence shows participation in cancer rehabilitation interventions may result in cost savings to survivors and the healthcare system [29][30][31]. ...
Article
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Simple Summary This is the first study to examine the impact of specialized community-based outpatient physical and occupational therapy on the health-related quality of life of cancer survivors with various cancers. Survivors who completed PT/OT reported significant improvements in physical and mental health, physical function, and social participation. Although more research is needed, these findings suggest cancer rehabilitation is an important strategy to meet HRQOL needs and lends support for inclusion as a standard of care. Abstract Compared to adults without cancer, cancer survivors report poorer health-related quality of life (HRQOL), which is associated with negative treatment outcomes and increased healthcare use. Cancer-specialized physical and occupational therapy (PT/OT) could optimize HRQOL; however, the impact among survivors with non-breast malignancies is unknown. This retrospective (2020–2022), observational, study of medical record data of 12 cancer types, examined pre/post-HRQOL among cancer survivors who completed PT/OT. PROMIS® HRQOL measures: Global Health (physical [GPH] and mental [GMH]), Physical Function (PF), and Ability to Participate in Social Roles and Activities (SRA) were evaluated using linear mixed effect models by cancer type, then compared to the minimal important change (MIC, 2 points). Survivors were 65.44 ± 12.84 years old (range: 19–91), male (54%), with a median of 12 visits. Improvements in GPH were significant (p < 0.05) for all cancer types and all achieved MIC. Improvements in GMH were significant for 11/12 cancer types and 8/12 achieved MIC. Improvements in PF were significant for all cancer types and all achieved the MIC. Improvements in SRA were significant for all cancer types and all groups achieved the MIC. We observed statistically and clinically significant improvements in HRQOL domains for each of the 12 cancer types evaluated.
... Kawabata et al.'s (2018) research participants, after engaging in the soup program, reported that they "felt [removed] from stress." These findings are similar to other research that showed that exercise, including routine activities, could provide physical and psychological health benefits for adults with terminal cancer (Hunter et al., 2017). In addition, Bieligmeyer et al.'s (2018) research supports the effect of physical and psychological comfort among clients with cancer by showing how patients with cancer who engaged in vibroacoustic music experienced better vital functions, vigilance, and mood. ...
Article
Importance: In this scoping review, we explore the meaning of occupation for people with advanced cancer to develop and improve occupation-based services in oncology. Objective: To identify the meaning(s) of occupation for adults with advanced cancer through relevant peer-reviewed literature. Data Sources: Scopus, CINAHL, Medline, and PubMed were used to identify peer-reviewed articles published between 2011 and 2021. Study Selection and Data Collection: Inclusion criteria comprised research studies in English and on meaningful occupations as well as participants age 19 yr or older and diagnosed with advanced cancer. Exclusion criteria comprised non-English publications, studies with participants in an early stage of cancer, and gray literature or nonreviewed articles. Findings: Thirteen articles matched the inclusion criteria: 9 qualitative studies, 1 mixed-methods study, 1 case study, 1 pilot study (pretest–posttest design), and 1 retrospective study (review of clinical data). Four themes emerged from the thematic analysis: occupation benefits important relationships and connections with others, occupation as a source of physical or psychological comfort, managing one’s identity through occupation, and occupation as a religious expression. Conclusions and Relevance: This scoping review highlights the value of participating in an occupation for people with advanced cancer. It also shows the importance of meaningful occupations to the quality of life and well-being of adults with advanced cancer. What This Article Adds: This scoping review identifies meanings of occupation linked to the health and well-being of adults with advanced cancer to develop and improve occupation-based services in oncology.
... All PLWBC are eligible to participate if the services are medically necessary. Availability of programming varies geographically, particularly between urban and rural settings (32)(33)(34). ...
Article
The evidence to support the benefits of exercise for people living with and beyond cancer is robust. Still, exercise oncology interventions in the United States are only eligible for coverage by third-party payers within the restrictions of cancer rehabilitation settings. Without expanded coverage, access will remain highly inequitable, tending toward the most well-resourced. This article describes the pathway to third-party coverage for 3 programs that address a chronic disease and utilize exercise professionals: the Diabetes Prevention Program, Supervised Exercise Training for Peripheral Artery Disease, and Cancer Rehabilitation. Lessons learned will be applied toward expanding third-party coverage for exercise oncology programming.
... With regards to quality of life, the sample appears to be neutral concerning its overall quality of life. These findings are in line with the results of other relevant studies conducted in the past [13][14][15][16][17]. Also, the literature gives us some information about the effect of the Occupational Therapy intervention on one or more of its dimensions Health-related Quality of life. ...
Article
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The aim of the present study is the investigation of the levels of quality of life and pain self-efficacy among chronic disease patients undergoing occupational therapy. The sample consists of 63 people, all chronic disease patients. Of the above patients, according to the research design, half receive Occupational Therapy services at a rate of 50.8% (32 patients) while the remaining 49.2% (31 people) did not receive. For the data collection MVQOLI-15 and PSEQ were used. We found that the average value of the sample regarding self-efficacy amounts to 39.10 (SD: 13.25), from which we can conclude that the sample appears moderately self-efficacious. Beyond this, the minimum value of self-efficacy amounts to 11,000 while the corresponding maximum to 64,00. Also, in general the sample appears to be neutral regarding its overall quality of life with the corresponding average value of the scale amounting to 15.86 ( SD: 3.09). The value range is found from 9.60 to 22.50, while the median value is 15.80.
Article
Background Older breast cancer survivors (BCS, age ≥ 65) are vulnerable to experiencing persistent symptoms and associated declines in health‐related quality of life (HRQOL). In research trials, cancer rehabilitation interventions (physical or occupational therapy, PT/OT) have been shown to enhance HRQOL, but the impact of community‐based PT/OT services for older BCS is unknown. We performed a retrospective, observational study to better understand the impact of PT/OT services on the HRQOL of older BCS. Methods Outcomes and covariates were extracted from the outpatient rehabilitation medical record. HRQOL outcomes included: PROMIS® global physical health (GPH), global mental health (GMH), physical function (PF), and ability to participate in social roles and activities (SRA). Linear mixed‐effect models were used to examine change in HRQOL outcomes and explore the influence of patient age and service type (PT/OT). ICD‐10 codes were examined and compared between service types to describe the impairments treated. Results PT/OT cases ( N = 694) were 71.79 ± 5.44 years old and participated in a median of 11 visits (IQR: 7.0–17.25) over 9.71 weeks (IQR: 6.29–15.29). Most (84.4%) attended PT ( n = 579; 84%) versus OT ( n = 115; 16%). Overall, significant improvement was observed in each HRQOL outcome (GPH: +3.00, p < 0.001; GMH: +1.80, p < 0.001; PF: +1.97, p < 0.001; SRA: +2.34, p < 0.001). Service type influenced only GPH ( p = 0.041); mean improvement was +3.24 (SE: 0.290, p < 0.001) for PT cases and + 1.78 for OT cases (SE: 0.651, p = 0.007). PT cases commonly received treatment for weakness/atrophy, pain, walking, and posture; OT cases commonly received treatment for lymphedema and scarring/fibrosis. No age effects were observed. Conclusions In this large study of older BCS who participated in community‐based PT/OT services across the United States, we observed significant improvements in HRQOL outcomes that are important to older BCS and their providers. Although more research is needed, these findings suggest that improved access to PT/OT could help address unmet HRQOL needs among this population.
Article
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Background: People living with advanced cancer experience functional decline and increasing difficulty participating in activities of daily living over their final year of life, consequently reducing quality of life. Palliative rehabilitation may serve to mitigate some of these challenges by optimising function. However, limited research and theory explore the rehabilitative process of adaptation amid increasing dependency, often experienced by people living with advanced cancer. Aim: To explore the lived experience of everyday life for working-aged adults living with advanced cancer, and how this changes over time. Design: A longitudinal hermeneutic phenomenological approach was employed, using in-depth semi-structured interviews. Data was analysed using inductive thematic analysis, and findings mapped against the Model of Human Occupation and illness experience literature. Setting/participants: Purposively sampled working-aged adults (40–64 years) with advanced cancer were recruited by a rural home care team in Western Canada. Results: Thirty-three in-depth interviews were conducted over 19 months with eight adults living with advanced cancer. Advanced cancer and other losses have a disruptive impact on daily life. Despite experiencing progressive functional decline, these adults intentionally sought to participate in valued everyday activities. Adaptation to ongoing deterioration occurred through engagement in daily life. Conclusions: Despite experiencing disruption to routines and daily life, people living with advanced cancer seek to continue doing what is important to them, albeit in a modified form. Adaptation to functional decline is an active, ongoing process and occurs through continued engagement in activities. Palliative rehabilitation can facilitate participation in everyday life.
Article
Background: People living with advanced cancer experience functional decline and increasing difficulty participating in activities of daily living over their final year of life, consequently reducing quality of life. Palliative rehabilitation may serve to mitigate some of these challenges by optimising function. However, limited research and theory explore the rehabilitative process of adaptation amid increasing dependency, often experienced by people living with advanced cancer. Aim: To explore the lived experience of everyday life for working-aged adults living with advanced cancer, and how this changes over time. Design: A longitudinal hermeneutic phenomenological approach was employed, using in-depth semi-structured interviews. Data was analysed using inductive thematic analysis, and findings mapped against the Model of Human Occupation and illness experience literature. Setting/participants: Purposively sampled working-aged adults (40–64 years) with advanced cancer were recruited by a rural home care team in Western Canada. Results: Thirty-three in-depth interviews were conducted over 19 months with eight adults living with advanced cancer. Advanced cancer and other losses have a disruptive impact on daily life. Despite experiencing progressive functional decline, these adults intentionally sought to participate in valued everyday activities. Adaptation to ongoing deterioration occurred through engagement in daily life. Conclusions: Despite experiencing disruption to routines and daily life, people living with advanced cancer seek to continue doing what is important to them, albeit in a modified form. Adaptation to functional decline is an active, ongoing process and occurs through continued engagement in activities. Palliative rehabilitation can facilitate participation in everyday life.
Article
The aim of the work is to review modern literary sources regarding the relevance of physical therapy and occupational therapy in cancer patients at the stage of palliative and hospice care. Results. The relevance of physical therapy and occupational therapy methods in palliative and hospice medicine for cancer patients was studied. It has been established that physical therapy and occupational therapy for oncological patients at the stage of palliative and hospice care has a high efficiency for various indicators, which ultimately leads to an improvement in the quality of life not only of patients but also of their family members who supervise. But on the other hand, physical therapy and occupational therapy are not used enough in this group of patients due to various reasons. Conclusion. The use of physical therapy and occupational therapy are relevant for palliative oncological patients. It is necessary to introduce it into the health care system more actively, considering the high efficiency of physical therapy and occupational therapy in the practice of interdisciplinary treatment approaches of oncological patients at the stage of palliative and hospice care.
Article
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This article is the second part of a systematic review of evidence for the effectiveness of cancer rehabilitation interventions within the scope of occupational therapy that address the activity and participation needs of adult cancer survivors. This article focuses on the use of multidisciplinary rehabilitation and interventions that address psychosocial outcomes, sexuality, and return to work. Strong evidence indicates that multidisciplinary rehabilitation benefits cancer survivors and that psychosocial strategies can reduce anxiety and depression. Moderate evidence indicates that interventions can support survivors in returning to the level of sexuality desired and help with return to work. Part 1 of the review also appears in this issue. © 2017, American Occupational Therapy Association, Inc. All rights reserved.
Article
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Systematic reviews and meta-analyses have become increasingly important in health care. Clinicians read them to keep up to date with their field [1],[2], and they are often used as a starting point for developing clinical practice guidelines. Granting agencies may require a systematic review to ensure there is justification for further research [3], and some health care journals are moving in this direction [4]. As with all research, the value of a systematic review depends on what was done, what was found, and the clarity of reporting. As with other publications, the reporting quality of systematic reviews varies, limiting readers' ability to assess the strengths and weaknesses of those reviews. Several early studies evaluated the quality of review reports. In 1987, Mulrow examined 50 review articles published in four leading medical journals in 1985 and 1986 and found that none met all eight explicit scientific criteria, such as a quality assessment of included studies [5]. In 1987, Sacks and colleagues [6] evaluated the adequacy of reporting of 83 meta-analyses on 23 characteristics in six domains. Reporting was generally poor; between one and 14 characteristics were adequately reported (mean = 7.7; standard deviation = 2.7). A 1996 update of this study found little improvement [7]. In 1996, to address the suboptimal reporting of meta-analyses, an international group developed a guidance called the QUOROM Statement (QUality Of Reporting Of Meta-analyses), which focused on the reporting of meta-analyses of randomized controlled trials [8]. In this article, we summarize a revision of these guidelines, renamed PRISMA (Preferred Reporting Items for Systematic reviews and Meta-Analyses), which have been updated to address several conceptual and practical advances in the science of systematic reviews (Box 1). Box 1: Conceptual Issues in the Evolution from QUOROM to PRISMA Completing a Systematic Review Is an Iterative Process The conduct of a systematic review depends heavily on the scope and quality of included studies: thus systematic reviewers may need to modify their original review protocol during its conduct. Any systematic review reporting guideline should recommend that such changes can be reported and explained without suggesting that they are inappropriate. The PRISMA Statement (Items 5, 11, 16, and 23) acknowledges this iterative process. Aside from Cochrane reviews, all of which should have a protocol, only about 10% of systematic reviewers report working from a protocol [22]. Without a protocol that is publicly accessible, it is difficult to judge between appropriate and inappropriate modifications.
Article
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This study aimed to explore functional deficits and perceived quality of life (QoL) among cancer survivors. Sixty-six participants completed the Post Cancer Outcome Survey developed for the purpose of this study. The results indicated (1) modest to moderate degrees of functional deficits in 28 of the 70 items measuring areas of occupation, performance skills, body functions, and psychosocial well-being within the first year after cancer treatment; (2) significantly lower perceived QoL during the first year of survivorship compared with that before diagnosis, at present, and 5 yr hereafter (p < .001); (3) significant moderate negative correlations between the reported functional deficits and QoL (rs = -.45 to -.57); and (4) a very low percentage of participants (4.5%) receiving occupational therapy during the first year posttreatment. Functional difficulties and compromised QoL identified in this study indicate the need for occupational therapy among cancer survivors. Increasing clients' awareness of occupational therapy for postcancer care is also suggested.
Article
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Cancer can cause multiple impairments, activity limitations and participation restrictions. According to individual case findings and needs, rehabilitation treatment is varied. The review mainly focuses on specific problems. Because of functional deficits cancer patients suffer from persistent emotional and social distress and a reduced quality of life (QOL). QOL encompasses at least the four dimensions of physical, emotional, social and cognitive function, which may be positively influenced by physical exercise. Physical exercise also has been shown to prevent or minimise inactivity/ disuse problems and to reduce fatigue. The management of sexuality dysfunction has to begin with a thorough history taking and a consequent sexuality counselling. The goals of rehabilitation procedures under palliative care are not only to control physical pain but also to help with mental, social and spiritual pain, together with other symptoms. Rehabilitation problems in head and neck cancer, sexuality, lung cancer, prostate cancer, breast cancer and lymphedema can be improved by rehabilitation. The review mainly focuses on impairment and activity limitation. Social, psychological and vocational aspects are left aside in this review.
Article
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Occupational therapy may significantly improve cancer survivors' ability to participate in activities, thereby improving quality of life. Little is known, however, about the use of occupational therapy services by adults with cancer. The objective of this study was to understand what shapes patterns of occupational therapy use to help improve service delivery. We examined older (age >65 yr) adults diagnosed with breast, prostate, lung, or melanoma (skin) cancer between 2004 and 2007 (N = 27,131) using North Carolina Central Cancer Registry data linked to Medicare billing claims. Survivors who used occupational therapy within 1 yr before their cancer diagnosis were more likely to use occupational therapy after diagnosis but also experienced the highest levels of comorbidities. Survivors with Stage 4 cancers or lung cancer were less likely to use occupational therapy. These findings suggest possible disparities in utilization of occupational therapy by older adults with cancer.
Article
Background: Lymphedema is an adverse effect of breast cancer surgery. Aqua lymphatic therapy (ALT) is a novel treatment for limb volume reduction. Objective: The aim of this study was to examine whether ALT is a safe method and whether there are differences in adherence, limb volume, and quality of life between women who perform only self-management treatment and women who participate as well in ALT. Design: Design of the study was single-blind randomized clinical trial. Setting: The setting was in a hydrotherapy pool, 1.2 m depth, and a temperature of 32-33 degrees capital ES, Cyrillic. Patients: Forty-eight women (56 +/- 10 years), with a 12.8% lymphedema relative volume, participated in the study. Intervention: The control group was instructed to perform the self-management treatment. The study group joined a weekly session of ALT for 3 months in addition to the self-management therapy. Measurements: Adherence was assessed by a self-reported diary, limb volume by a water displacement device, quality of life by the Upper Limb Lymphedema Questionnaire (ULL27), prior to, and after the intervention period. Results: There was no episode of arm infection or aggravation in limb volume during the study period. ALT had a positive, statistically and clinically significant immediate effect on limb volume but no long-term effect was noted. The adherence rate to ALT was significantly higher than the adherence to self-management therapy. QOL improved in the study group. Conclusion: ALT was found to be a safe method, with high adherence, in treating women who suffer from mild to moderate lymphedema. A significant immediate and insignificant long-term effect on limb volume was noted.
Article
Purpose: Individualized outcome measure used to detect changes in the self-perception of the client's performance and satisfaction over time by identifying problems in performing activities of daily living Target Population: There is no limit placed on age or diagnoses when using the COPM. However when using the COPM when assessing young children, parents can become the clients and answer questions in regards to their child's abilities. What it Tests: The five most important problems in performing activities of daily living according to the individual patient will be determined through a 10 point scale that will provide a guideline for rehabilitation.
Article
This is the first study to use meta-analysis as a scientific technique to provide an integrated analysis of the effectiveness of music intervention in cancer patients. The purpose of this study was, using the meta-analysis method, to present a summary of existing research and explore the effectiveness of music intervention in ameliorating anxiety, depression, pain, and fatigue in cancer patients. The present study collected quantitative study designs sought of music intervention for cancer patients published from 2002 to 2012. These studies were then cross-referenced using Medical Subject Headings for topics on music intervention and cancer patients. Outcome indicators were anxiety, depression, pain, and fatigue. The quality of the studies was evaluated using Cochrane Collaboration Guidelines. The effect size on outcome indicators used the formula devised by Hedges and Olkin (1985). Results showed that music interventions were significantly effective in ameliorating anxiety (g = -0.553), depression (g = -0.510), pain (g = -0.656), and fatigue (g = -0.422) in cancer patients. Subgroup analyses revealed that age and who selected the music were major factors influencing the effect size on anxiety reduction. Music interventions significantly ameliorate anxiety, depression, pain, and fatigue in cancer patients, especially adults. Music interventions were more effective in adults than in children or adolescents and more effective when patients, rather than researchers, chose the music. Our findings provide important information for future music-intervention planners to improve the design and processes that will benefit patients in such programs.
Article
Cancer is a leading cause of death worldwide. Mind-body interventions are widely used by cancer patients to reduce symptoms and cope better with disease- and treatment-related symptoms. In the last decade, many clinical controlled trials of qigong/tai chi as a cancer treatment have emerged. This study aimed to quantitatively evaluate the effects of qigong/tai chi on the health-related outcomes of cancer patients. Five databases (Medline, CINAHL, Scopus, the Cochrane Library, and the CAJ Full-text Database) were searched until June 30, 2013. Randomized controlled trials (RCTs) of qigong/tai chi as a treatment intervention for cancer patients were considered for inclusion. The primary outcome for this review was changes in quality of life (QOL) and other physical and psychological effects in cancer patients. The secondary outcome for this review was adverse events of the qigong/tai chi intervention. A total of 13 RCTs with 592 subjects were included in this review. Nine RCTs involving 499 subjects provided enough data to generate pooled estimates of effect size for health-related outcomes. For cancer-specific QOL, the pooled weighted mean difference (WMD) was 7.99 [95% confidence interval (CI): 4.07, 11.91; Z score=4.00, p<0.0001]. The standardized mean differences (SMDs) for changes in depression and anxiety score were -0.69 (95% CI: -1.51, 0.14; Z score=1.64, p=0.10), and -0.93 (95% CI: -1.80, -0.06; Z score=2.09, p=0.04), respectively. The WMDs for changes in body mass index and body composition from baseline to 12 weeks follow-up were -1.66 (95% CI: -3.51, 0.19; Z score=1.76, p=0.08), and -0.67 (95% CI: -2.43, 1.09; Z score=0.75, p=0.45) respectively. The SMD for changes in the cortisol level was -0.37 (95% CI: -0.74, -0.00; Z score=1.97, p=0.05). This study found that qigong/tai chi had positive effects on the cancer-specific QOL, fatigue, immune function and cortisol level of cancer patients. However, these findings need to be interpreted cautiously due to the limited number of studies identified and high risk of bias in included trials. Further rigorous trials are needed to explore possible therapeutic effects of qigong/tai chi on cancer patients.