cM1 beta values in all eleven Participants (P1… P11). Individual cM1 beta values during baseline imagery, the three neurofeedback runs (NF run1, run2, run3) and the average across runs (Avg NF runs).

cM1 beta values in all eleven Participants (P1… P11). Individual cM1 beta values during baseline imagery, the three neurofeedback runs (NF run1, run2, run3) and the average across runs (Avg NF runs).

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Motor imagery (MI) has shown effectiveness in enhancing motor performance. This may be due to the common neural mechanisms underlying MI and motor execution (ME). The main region of the ME network, the primary motor cortex (M1), has been consistently linked to motor performance. However, the activation of M1 during motor imagery is controversial, w...

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... Operant investigated for decades [2,3], primarily at the level of the brain [4]. In this manner, an individual learns to self-modulate a neural circuit, with the implication of neuroplastic changes [4][5][6][7]. LaCroix [8] hypothesized that in operant conditioning there are both implicit automatic learning processes occurring in parallel with explicit ones. However, these processes combined with physiology of a complex brain circuit is a poorly understood process [4]. ...
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... This approach has shown substantial signal modulation in both healthy individuals [53][54][55] and neurological patients [48,49,52,56]. In contrast, studies using fMRI neurofeedback to train primary motor cortex (M1) upregulation reported inconsistent results: while some studies found no significant modulation [57,58], one study reported activation only for a subset of participants [59], and other studies reported even deactivation of M1 [54,60]. The neurophysiological basis for these inconsistent findings, particularly the lack of BOLD activation in M1 during motor imagery, has been a matter of debate [43,54]. ...
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... MI-NFB has been reported to provide feedback on activity in the primary motor cortex (M1) [38,39] and supplementary motor area (SMA) [40,41] in many studies. These areas are activated by motor imagery and have been reported to be related to the accuracy of motor imagery [31]. ...
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... The selfregulation of neural activity through neurofeedback training has been found in rodents, nonhuman primates and humans (Schafer and Moore, 2011;Collinger et al., 2013;Clancy et al., 2014). The consequence of this self-regulation can be represented as changes in intracortical neuronal synchronization that facilitate the output of EEG-based BCI (Hanslmayr et al., 2005;Blefari et al., 2015). Moreover, neurofeedback training can also exert long-term changes in the intrinsic functional connectivity in the visuo-spatial-motor network, even more than 2 months after the training (Megumi et al., 2015). ...
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The brain-computer interface (BCI)-mediated rehabilitation is emerging as a solution to restore motor skills in paretic patients after stroke. In the human brain, cortical motor neurons not only fire when actions are carried out but are also activated in a wired manner through many cognitive processes related to movement such as imagining, perceiving, and observing the actions. Moreover, the recruitment of motor cortexes can usually be regulated by environmental conditions, forming a closed-loop through neurofeedback. However, this cognitive-motor control loop is often interrupted by the impairment of stroke. The requirement to bridge the stroke-induced gap in the motor control loop is promoting the evolution of the BCI-based motor rehabilitation system and, notably posing many challenges regarding the disease-specific process of post stroke motor function recovery. This review aimed to map the current literature surrounding the new progress in BCI-mediated post stroke motor function recovery involved with cognitive aspect, particularly in how it refired and rewired the neural circuit of motor control through motor learning along with the BCI-centric closed-loop.
... Crucially, recording of the actual force trace during scan acquisition allowed the use of MVC-normalized task regressors. Brain motor-task studies have used recorded force data in fMRI models to account for timing differences by defining task and rest blocks (Shanahan et al., 2015), by creating a force nuisance regressor to remove effects related to the actual achieved force or unintended exertion (Blefari et al., 2015;Haller et al., 2009) ...
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... MI comes in two flavors: visual imagination (VI) and kinaesthetic imagination (KI) [11]. MI has a significant function since it is often utilized in motor learning exercises [12]. It may be beneficial to athletes, skill development, and rehabilitation since it may be used to improve motor performance over periods [13]. ...
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... More than half of the reviewed studies engaged healthy volunteers to probe the feasibility of NF training in FSC regions. These studies sought to modify behavioral aspects such as emotion regulation , motor performance (Hui et al., 2014;Blefari et al., 2015;Scharnowski et al., 2015;Al-Wasity et al., 2021), motivation , working memory Sherwood et al., 2016), speech processing (Rota et al., 2009) and social avoidance (Lisk et al., 2020) with their results underscoring the relevance of the functional organization of the FSC. The studies that aimed to improve motor performance focused on regions in the motor subsystem, such as the M1, the SMA, and the PMA. ...
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Dysregulated frontostriatal circuitries are viewed as a common target for the treatment of aberrant behaviors in various psychiatric and neurological disorders. Accordingly, experimental neurofeedback paradigms have been applied to modify the frontostriatal circuitry. The human frontostriatal circuitry is topographically and functionally organized into the “limbic,” the “associative,” and the “motor” subsystems underlying a variety of affective, cognitive, and motor functions. We conducted a systematic review of the literature regarding functional magnetic resonance imaging-based neurofeedback studies that targeted brain activations within the frontostriatal circuitry. Seventy-nine published studies were included in our survey. We assessed the efficacy of these studies in terms of imaging findings of neurofeedback intervention as well as behavioral and clinical outcomes. Furthermore, we evaluated whether the neurofeedback targets of the studies could be assigned to the identifiable frontostriatal subsystems. The majority of studies that targeted frontostriatal circuitry functions focused on the anterior cingulate cortex, the dorsolateral prefrontal cortex, and the supplementary motor area. Only a few studies ( n = 14) targeted the connectivity of the frontostriatal regions. However, post-hoc analyses of connectivity changes were reported in more cases ( n = 32). Neurofeedback has been frequently used to modify brain activations within the frontostriatal circuitry. Given the regulatory mechanisms within the closed loop of the frontostriatal circuitry, the connectivity-based neurofeedback paradigms should be primarily considered for modifications of this system. The anatomical and functional organization of the frontostriatal system needs to be considered in decisions pertaining to the neurofeedback targets.
... The findings of this study might be useful to guide brain-targeted interventions. Areas such as the SMA [67], premotor cortex [68], and primary motor cortex [69] have been the target for upregulation in neurofeedback studies, consequently increasing their functional connectivity to other brain regions. Neurofeedback interventions also target connectivity between motor regions directly [70]. ...
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... NF refers to a procedure in which contingent feedback of motor-related neural activity is presented to the participants via visual or audio signals [12,13], haptic stimulation [14,15], or kinaesthetic representations assisted by robotic devices [16][17][18] to facilitate the regulation of neural patterns. As the most widely used paradigm for neurorehabilitation, motor imagery (MI)-based NF training has been proven useful in improving impaired motor cortical activity in patients [19][20][21]. These MI-based NF studies have typically focused on training the modulation of sensorimotor rhythms (SMRs) that are oscillations occurring in the alpha and beta bands recorded by electroencephalogram over the sensorimotor areas during MI [22][23][24][25]. ...
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Objective. Investigating how to promote the functional activation of the central sensorimotor system is an important goal in the neurorehabilitation research domain. We aim to validate the effectiveness of facilitating cortical excitability using a closed-loop visuomotor task, in which the task difficulty is adaptively adjusted based on an individual’s sensorimotor cortical activation. Approach. We developed a novel visuomotor task, in which subjects moved a handle of a haptic device along a specific path while exerting a constant force against a virtual surface under visual feedback. The difficulty levels of the task were adapted with the aim of increasing the activation of sensorimotor areas, measured non-invasively by functional near-infrared spectroscopy. The changes in brain activation of the bilateral prefrontal cortex, sensorimotor cortex, and the occipital cortex obtained during the adaptive visuomotor task (adaptive group), were compared to the brain activation pattern elicited by the same duration of task with random difficulties in a control group. Main results. During one intervention session, the adaptive group showed significantly increased activation in the bilateral sensorimotor cortex, also enhanced effective connectivity between the prefrontal and sensorimotor areas compared to the control group. Significance. Our findings demonstrated that the fNIRS-based adaptive visuomotor task with high ecological validity can facilitate the neural activity in sensorimotor areas and thus has the potential to improve hand motor functions.
... It also served to assess motor performance of the participants. We used the raw data from the force sensors to locate individual tap onsets (force derivative, Ḟ , above 10% of maximum, as in (Blefari et al., 2015) and calculated reaction times for the externally-cued task as the time difference between cue and tap onset. To test for agreement in motor performance between the externally-cued and self-paced experiments, mean tapping frequencies and mean peak forces ( Fig. 1) were correlated, indicating good protocol adherence and comparable motor output (Bichsel et al., 2018). ...
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Deep brain stimulation (DBS) electrodes provide an unparalleled window to record and investigate neuronal activity right at the core of pathological brain circuits. In Parkinson's disease (PD), basal ganglia beta-oscillatory activity (13–35 Hz) seems to play an outstanding role. Conventional DBS, which globally suppresses beta-activity, does not meet the requirements of a targeted treatment approach given the intricate interplay of physiological and pathological effects of beta-frequencies. Here, we wanted to characterise the local field potential (LFP) in the subthalamic nucleus (STN) in terms of beta-burst prevalence, amplitude and length between movement and rest as well as during self-paced as compared to goal-directed motor control. Our electrophysiological recordings from externalised DBS-electrodes in nine patients with PD showed a marked decrease in beta-burst durations and prevalence during movement as compared to rest as well as shorter and less frequent beta-bursts during cued as compared to self-paced movements. These results underline the importance of beta-burst modulation in movement generation and are in line with the clinical observation that cued motor control is better preserved than self-paced movements. Furthermore, our findings motivate the use of adaptive DBS based on beta-bursts, which selectively trim longer beta-bursts, as it is more suitable and efficient over a range of motor behaviours than conventional DBS.