Luo FG, Wang JJ, Xing HY, Wu WY, Fang KJ, Yan J. Integrating electromyographic biofeedback in stroke rehabilitation: A paradigm shift in motor and psychological recovery. World J Psychiatry 2026; 16(2): 115160 [DOI: 10.5498/wjp.v16.i2.115160]
Corresponding Author of This Article
Juan Yan, MD, Professor, Quality Control Office, Affiliated Mental Health Center, Zhejiang University School of Medicine, Hangzhou Seventh People’s Hospital, No. 305 Tianmushan Road, Xihu District, Hangzhou 310013, Zhejiang Province, China. 294162939@qq.com
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Psychiatry
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Editorial
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This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Feb 19, 2026 (publication date) through Feb 2, 2026
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World Journal of Psychiatry
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2220-3206
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Luo FG, Wang JJ, Xing HY, Wu WY, Fang KJ, Yan J. Integrating electromyographic biofeedback in stroke rehabilitation: A paradigm shift in motor and psychological recovery. World J Psychiatry 2026; 16(2): 115160 [DOI: 10.5498/wjp.v16.i2.115160]
Fu-Gang Luo, Intensive Care Unit, Affiliated Mental Health Center, Zhejiang University School of Medicine, Hangzhou Seventh People’s Hospital, Hangzhou 310013, Zhejiang Province, China
Jun-Jie Wang, Judicial Appraisal Institute, Affiliated Mental Health Center, Zhejiang University School of Medicine, Hangzhou Seventh People’s Hospital, Hangzhou 310013, Zhejiang Province, China
Hao-Yu Xing, Department of Medical Engineering, Affiliated Mental Health Center, Zhejiang University School of Medicine, Hangzhou Seventh People’s Hospital, Hangzhou 310013, Zhejiang Province, China
Wen-Ye Wu, Kai-Jie Fang, Juan Yan, Quality Control Office, Affiliated Mental Health Center, Zhejiang University School of Medicine, Hangzhou Seventh People’s Hospital, Hangzhou 310013, Zhejiang Province, China
Co-corresponding authors: Hao-Yu Xing and Juan Yan.
Author contributions: Luo FG and Wang JJ contributed to the conceptualization, writing, and they contributed equally to this manuscript and are co-first authors; Xing HY and Yan J drafted the manuscript, and they contributed equally to this manuscript and are co-corresponding authors; Wu WY and Fang KJ contributed to the review and editing. All the authors have read and approved the final version of the manuscript.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
Open Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Juan Yan, MD, Professor, Quality Control Office, Affiliated Mental Health Center, Zhejiang University School of Medicine, Hangzhou Seventh People’s Hospital, No. 305 Tianmushan Road, Xihu District, Hangzhou 310013, Zhejiang Province, China. 294162939@qq.com
Received: October 9, 2025 Revised: November 3, 2025 Accepted: December 8, 2025 Published online: February 19, 2026 Processing time: 113 Days and 3.1 Hours
Abstract
A retrospective study by Yu et al demonstrated the efficacy of adding electromyographic biofeedback to conventional rehabilitation in improving motor function and reducing anxiety in stroke survivors. This editorial contextualizes these findings within emerging neurorehabilitation trends, highlighting the shift toward integrated approaches that address physical and psychological sequelae. Pooled data from 15 studies (n = 1850) revealed that electromyographic biofeedback enhanced Fugl-Meyer Assessment scores for the upper (Cohen’s d = 0.82) and lower limbs (d = 0.79), while reducing anxiety (Hamilton Anxiety Rating Scale: d = -0.75) and depression (Hamilton Depression Rating Scale: d = -0.71). Proposed mechanisms include enhanced neuroplasticity, improved motor unit recruitment, and real-time, feedback-driven self-regulation. We discuss the clinical implications of standardizing biofeedback protocols and address scalability in resource-limited settings. Future research should prioritize randomized controlled trials, neuroimaging correlates, and cost-effectiveness analyses.
Core Tip: Electromyographic biofeedback demonstrates significant dual benefits in stroke rehabilitation, improving motor function (Fugl-Meyer Assessment: d = 0.79-0.82) and reducing anxiety (Hamilton Anxiety Scale: d = -0.75) compared to conventional therapy alone. The mechanism involves Hebbian plasticity through real-time visual/auditory feedback, creating a virtuous cycle of neuroplastic change and psychological empowerment. Despite implementation challenges (5000-15000 startup costs), the 2-3 weeks faster functional recovery yields 8000-12000 per-patient savings, supporting integration into value-based care models. Optimal protocols involve 45-minute sessions targeting agonist-antagonist pairs 4 times weekly for 8-12 weeks, with future research needed for personalized application in severe stroke cases.
Citation: Luo FG, Wang JJ, Xing HY, Wu WY, Fang KJ, Yan J. Integrating electromyographic biofeedback in stroke rehabilitation: A paradigm shift in motor and psychological recovery. World J Psychiatry 2026; 16(2): 115160
Stroke remains a leading cause of long-term disability worldwide, with up to 80% of survivors experiencing motor impairment and 30% developing anxiety or depression[1]. Yu et al’s study[2] adds to evidence supporting electromyographic (EMG) biofeedback as an adjunct to conventional rehabilitation. Their findings - significant improvements in Fugl-Meyer Assessment (FMA) scores (upper limb: 36.83 vs 29.50; lower limb: 26.73 vs 22.53) and reduced Hamilton Anxiety Rating Scale (HAMA) scores (7.93 vs 9.73) in the biofeedback group - align with a paradigm shift toward multimodal, patient-centered interventions[2,3]. These editorial critiques these results from three perspectives: (1) Comparative efficacy vs other therapies; (2) Neuroplasticity mechanisms; and (3) Implementation barriers. Integration of EMG biofeedback represents a major advancement in addressing the interplay between physical rehabilitation and psychological well-being during stroke recovery[4]. By providing patients with real-time physiological data, this approach empowers active participation in rehabilitation, potentially enhancing both motor outcomes and emotional resilience[5]. As healthcare systems increasingly prioritize value-based care, evidence supporting multimodal interventions, such as EMG biofeedback, becomes crucial for designing efficient and effective rehabilitation pathways[6].
EFFICACY TRENDS AND COMPARATIVE ANALYSIS
Yu et al’s results[2] are consistent with meta-analyses of EMG biofeedback in stroke rehabilitation[7]. As shown in Table 1, aggregated data from 15 studies confirm its superiority over conventional therapy alone. Notably, EMG biofeedback yields larger effect sizes in motor recovery than functional electrical stimulation [FMA for upper limb (FMA-UL): d = 0.82 vs 0.61] and comparable psychological benefits to cognitive-behavioral therapy (HAMA: d = -0.75 vs -0.70)[8]. However, significant heterogeneity exists across these studies due to variations in patient characteristics (e.g., age, stroke severity, lesion sites), rehabilitation settings, and biofeedback protocols (e.g., session frequency, duration). Such variability may influence effect sizes and generalizability, necessitating cautious interpretation of pooled results.
Table 1 Pooled efficacy of electromyographic biofeedback in stroke rehabilitation (k = 15 studies, n = 1850).
The temporal pattern of improvement warrants attention: Whereas conventional therapy produced modest 4-week gains (FMA-UL: Δ = +8.7 points), the biofeedback group demonstrated faster recovery (Δ = +10.57), suggesting that early biofeedback may capitalize on post-stroke neuroplasticity windows[4]. This acceleration has important implications for healthcare economics, as reduced time to functional recovery could decrease inpatient rehabilitation costs[6]. Subgroup analyses revealed that patients with moderate initial impairment (FMA-UL baseline: 15-25) benefited most (d = 0.91), whereas those with severe impairment (FMA-UL < 15) showed more modest gains (d = 0.63)[7]. This gradient supports patient stratification during clinical implementation[9]. Furthermore, the durability of benefits remains a key consideration. Studies with a six-month follow-up showed sustained improvement in biofeedback groups (FMA-UL retention: 92% of gains) vs a gradual decline in conventional therapy (retention: 78%), highlighting potential for long-term functional preservation[10].
MECHANISTIC INSIGHTS: BEYOND MOTOR RECOVERY
EMG biofeedback’s benefits extend beyond motor relearning[4]. By providing real-time visual and auditory feedback on muscle activity, EMG biofeedback promotes cortical reorganization via Hebbian plasticity[11]. Studies using functional magnetic resonance imaging have demonstrated increased activation in the contralateral motor cortices and cerebellar regions post-biofeedback, correlating with FMA improvements (r = 0.67, P < 0.01). Additionally, anxiety reduction may stem from restored agency: Patients regain control over paralyzed limbs, mitigating helplessness[12]. HAMA score reductions in Yu et al[2] (Δ = -1.8 in biofeedback group) support this hypothesis[2]. This mechanism involves reinforcement-learning loops, in which successful movement attempts strengthen corticospinal pathways through N-methyl-D-aspartate receptor-mediated synaptic potentiation[4]. Simultaneously, visualizing muscle activation provides tangible evidence of progress, countering the negative cognitive biases common in post-stroke depression[13]. Neurochemical studies suggest that biofeedback may normalize dysregulated hypothalamic-pituitary-adrenal axis activity, reducing cortisol levels and associated anxiety symptoms[14]. This dual-pathway mechanism, combining neural circuit reorganization with psychological empowerment, explains why EMG biofeedback outperforms modalities targeting either domain alone.
CLINICAL AND ECONOMIC IMPLICATIONS
Although effective, EMG biofeedback faces barriers, such as training requirements, cost considerations, and protocol standardization[6]. Therapists require specialized training - typically 40-60 hours in electrophysiology and biofeedback software - which represents a significant investment[15]. This barrier can be mitigated through tiered certification programs and telehealth supervision models[6]. Equipment costs present another hurdle. The initial setup for a clinical unit (surface EMG sensors, software licenses, and display interfaces) ranges from 5000-15000 dollars, with approximately 1000 dollars in annual maintenance[7]. However, cost-effectiveness analyses demonstrate potential savings from reduced rehabilitation duration - biofeedback groups achieve functional milestones 2-3 weeks faster than conventional therapy - translating to savings of 8000-12000 dollars per patient in indirect medical costs[8]. Protocol standardization remains elusive, with significant variations in session frequency (3-5 times weekly), duration (30-60 minutes), and target muscle groups across studies[3]. To address this, international consensus panels have begun developing evidence-based guidelines recommending 45-minute sessions targeting agonist-antagonist muscle pairs 4 times weekly for 8-12 weeks[5]. Implementation in low-resource settings requires innovative approaches such as simplified EMG devices costing under 500 dollars and task shifting to trained community health workers under specialist supervision[6]. Successful implementation strategies include phased rollouts beginning with tertiary centers, train-the-trainer models, and integration with existing stroke rehabilitation pathways rather than parallel systems[9].
LIMITATIONS AND FUTURE DIRECTIONS
Yu et al’s study[2] shares common limitations: Retrospective design, small sample size (n = 60), and short follow-up (8 weeks)[2] (Table 2). The retrospective nature introduces potential selection bias, as patients receiving biofeedback may have differed in unmeasured characteristics such as motivation or socioeconomic status[1]. The limited sample size reduces the statistical power of subgroup analyses, particularly when examining differences across stroke type (ischemic vs hemorrhagic) and lesion locations[10]. The 8-week follow-up period captures initial recovery but misses long-term outcomes critical to assessing sustained benefits[13]. Although pooled data show consistent significance, some individual trials report neutral or modest effects, especially in patients with severe strokes or comorbidities[7]. For example, a subgroup analysis by Chalard et al[7] found no significant FMA-UL improvement in patients with bilateral lesions (d = 0.21, P = 0.15), highlighting the need for nuanced patient selection.
Table 2 Implementation framework for electromyographic biofeedback in stroke rehabilitation.
Domain
Recommendation
Evidence level
Session frequency
3-5 sessions/week for 8 weeks
Meta-analysis (k = 10)
Duration per session
30-45 minutes
RCT (n = 300)
Muscle groups
Focus on agonist-antagonist pairs (e.g., wrist flexors/extensors)
Future research should address these limitations through multicenter randomized controlled trials with sample sizes exceeding 200 participants, incorporating stratified randomization by stroke severity and type[14]. Extended follow-up periods of 6-12 months are essential to evaluate the durability and effects on quality-of-life metrics[12]. Neuroimaging biomarkers represent another priority; functional magnetic resonance imaging and diffusion tensor imaging can identify neural correlates of treatment response, potentially leading to predictive models for personalizing therapy[11]. Economic evaluations comparing biofeedback with other interventions (e.g., robotics and virtual reality) should quantify cost per quality-adjusted-life-year metrics to guide resource allocation[8]. Technology development must focus on affordable, user-friendly EMG systems for home-based rehabilitation, leveraging smartphone integration and wireless sensors[7]. Finally, implementation science studies should identify optimal strategies for integrating biofeedback into diverse healthcare systems, particularly in low-resource settings, where stroke burden is highest[6]. Such coordinated efforts across basic, clinical, and implementation research will maximize the real-world impact of EMG biofeedback on global stroke rehabilitation[9].
CONCLUSION
Yu et al[2] reinforced EMG biofeedback’s role as a transformative tool in stroke rehabilitation. By simultaneously addressing motor and psychological recovery, the study exemplifies the holistic approach required in modern neurorehabilitation[4]. Evidence demonstrates consistent benefits across multiple functional domains, with effect sizes surpassing those of conventional therapy alone[7]. These mechanisms involve both neuroplastic changes and psychological empowerment, creating a virtuous cycle of improvement[11]. However, heterogeneity in patient populations and protocols, along with mixed results in severe cases, underscores the need for personalized application. Although implementation challenges exist, particularly regarding costs and training, these can be overcome through technological innovation and strategic planning[6]. Prioritizing accessibility, protocol standardization, and mechanistic research will unlock its full potential[14]. As healthcare systems worldwide grapple with rising stroke prevalence and limited resources, EMG biofeedback represents a promising approach to enhance recovery efficiency and comprehensiveness[1]. Future research should build on these foundations to establish personalized application protocols and expand global access to diverse patient populations[3].
Footnotes
Provenance and peer review: Invited article; Externally peer reviewed.
Peer-review model: Single blind
Specialty type: Psychiatry
Country of origin: China
Peer-review report’s classification
Scientific Quality: Grade C
Novelty: Grade C
Creativity or Innovation: Grade B
Scientific Significance: Grade C
P-Reviewer: Deng ZD, PhD, China S-Editor: Zuo Q L-Editor: A P-Editor: Zhang L
Haas MC, Sommer BB, Karrer S, Jörger M, Graf ES, Huber M, Baumgartner D, Bansi J, Kool J, Bauer CM. Surface electromyographic activity of trunk muscles during trunk control exercises for people after stroke; effect of a mobile and stable seat for rehabilitation.PLoS One. 2022;17:e0272382.
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