Effectiveness of virtual reality-supported exercise therapy in improving upper extremity function and activities of daily living among patients after stroke: a systematic review of randomized control trials

Article information

Osong Public Health Res Perspect. 2024;.j.phrp.2023.0148
Publication date (electronic) : 2024 March 8
doi : https://doi.org/10.24171/j.phrp.2023.0148
1Faculty of Nursing, Uttar Pradesh University of Medical Sciences, Uttar Pradesh, India
2Department of Nursing, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India
3College of Nursing, All India Institute of Medical Sciences, Jodhpur, India
Corresponding author: Nipin Kalal College of Nursing, All India Institute of Medical Sciences, Pin-342005, Jodhpur, India E-mail: kalalnipin@gmail.com
Received 2023 June 2; Revised 2024 January 19; Accepted 2024 February 6.

Abstract

This systematic review describes the effectiveness of virtual reality (VR)-supported exercise therapy on upper limb motor function and activities of daily living after stroke. Studies published through January 24, 2022, were identified using CINAHL, Cochrane Library, Embase, Medline, and Web of Science. Randomized control trials comparing VR treatment with conventional therapy (CT) for upper extremity rehabilitation after stroke were included. Methodological quality was assessed using the Cochrane risk-of-bias tool. Of 9 included studies, 5 concluded that the VR group outperformed control participants, 1 indicated the superiority of VR-supported exercises alone over CT, and 3 found VR comparable to CT in promoting upper limb motor function. Five studies analyzed independence in daily living, with 4 reporting no significant difference between VR and CT groups. No strong evidence indicated long-term benefits of VR-assisted exercise. All included studies demonstrated low risk of bias concerning random sequence generation, allocation concealment, outcome assessment blinding, incomplete outcome data, and selective reporting bias. However, a high risk of bias was observed regarding participant blinding due to the nature of the intervention. Most studies suggested that VR, used alongside CT, can improve motor function following stroke. However, the evidence was insufficient to conclude that VR outperforms conventional approaches.

Introduction

Stroke is the second leading cause of death worldwide, with an annual mortality figure of approximately 5.5 million deaths [1]. Additionally, up to 50% of survivors experience a permanent disability [2]. Stroke is characterized by neurological deficits and long-term disability resulting from a focal injury to the central nervous system, such as cerebral infarction, intracerebral hemorrhage, or subarachnoid hemorrhage [3].

Changes related to impaired upper arm function include difficulty performing tasks, abnormal postural adjustments, an inability to control grasping, and functional disability. These challenges make it difficult for individuals to participate in activities of daily living (ADLs) such as eating, dressing, and grooming [4,5]. Research indicates that 40% of stroke survivors experience reduced function in the affected arm, and approximately 70% of patients report diminished arm function [6]. Separately, over 80% of patients have been found to exhibit impaired upper limb motor function after stroke, with 66% continuing to have a non-functional upper limb long-term [7,8]. Upper limb impairments are often more pronounced than those of the lower limb [9] and include functional limitations and uncoordinated motion [10]. Conventional rehabilitation techniques such as physiotherapy, neurodevelopmental therapy, and proprioceptive neuromuscular facilitation are effective to similar degrees in improving motor function. However, these methods can be resource-intensive and costly, often requiring specialized facilities that are not widely available. Virtual reality (VR) has emerged as a novel rehabilitation strategy and an enjoyable alternative to enhance motor recovery after stroke [11,12]. VR is an emerging technology that provides an interactive simulation, creating an environment that closely mimics reality for users. VR has been described as “the use of interactive simulations created with computer hardware and software to present users with opportunities to engage in environments that appear and feel similar to real-world objects and events” [13]. VR is based on several principles, including goal-oriented tasks, adjustable task difficulty, task repetition, feedback, and the promotion of increased user motivation and enjoyment [14]. VR systems can be categorized as immersive or non-immersive. Non-immersive VR systems allow users to interact with the virtual environment displayed on a computer screen while maintaining a sense of the real world. Immersive VR systems, which include large screen projections, head-mounted displays, or Cave Automatic Virtual Environment (Balance Near Automatic Virtual Environment) systems, block out all real-world perception, immersing the user solely in computer-generated imagery [15].

Adults with persistent hemiparesis have recently been shown to benefit from VR therapy, with reasonably good patient compliance [16]. Engaging in physical exercises through VR programs can help patients with neurological disorders enhance their motor learning and control, as well as their functional capacities [17]. Research suggests that training in fine hand-motion rehabilitation can be more effective when it incorporates immersive VR technology [18]. Several studies have indicated that VR technology produces better outcomes than conventional therapies in improving upper extremity function [1924] and ADL performance [2224] after stroke. However, a systematic review conducted by Laver et al. [25] reported no appreciable difference between VR-based training and conventional treatment in the recovery of upper limb motor function. Due to the variability of findings regarding VR intervention, a systematic review is necessary to thoroughly explore the effects of VR rehabilitation on upper arm function. The aim of this review was to evaluate the benefits of VR in the motor recovery of upper limb function and in promoting independence in ADLs, focusing on studies conducted a maximum of 2 years after stroke.

Materials and Methods

Eligibility Criteria

We conducted this systematic review in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines (Supplementary Material 1). We incorporated studies that met the following inclusion criteria: (1) randomized controlled trials (RCTs) that compared VR with conventional interventions in upper limb rehabilitation, with no more than 2 years elapsed since the stroke, and that met predefined PICOTS criteria (Table 1); (2) the intervention group received VR-supported exercise therapy either alone or in combination with conventional therapy, while the control group received conventional therapy, recreational therapy, or standard care alone; (3) the study participants were at least 18 years old with any type of stroke (hemorrhagic or ischemic); and (4) the article was accessible and written in English. We excluded studies that compared 2 types of VR treatment, those involving robotics-supported therapy or VR treatment administered through telerehabilitation, and those conducted in home settings. Studies that included participants with cognitive impairments and those that did not focus exclusively on upper limb function were also excluded.

PICOTS criteria for included studies

Search Strategy

This review was conducted between October 2022 and March 2023. All reviewers independently performed a literature search across 5 databases: CINAHL, Cochrane Library, Embase, Medline, and Web of Science. The keywords used for the literature search were “stroke,” “cerebrovascular accident,” “virtual reality,” “virtual environment,” “motor deficits,” “neurorehabilitation,” and “upper limb function.” These keywords were used either individually or in combination, employing the Boolean operators “OR” and “AND”. No restrictions were imposed on the year of publication, and the most recent study publication date was January 24, 2022.

Outcome Measures

The primary outcome was upper limb function and activity, while the secondary outcomes were independence in daily living and the long-term benefits of VR therapy. We conducted a narrative synthesis of data from the identified studies, which encompassed participant characteristics, attributes of the interventional and control groups, upper limb function and activity, independence in ADLs, and the effects of VR therapy during the follow-up period.

Data Collection and Processing

The screening procedure was performed independently by 2 reviewers to identify relevant studies based on predetermined eligibility criteria. Initially, the titles of potential studies were screened, followed by an examination of the abstracts and full texts of the articles for inclusion in the review. Studies were assessed against the inclusion and exclusion criteria before being selected. Data from the articles were extracted and analyzed independently by the first 2 reviewers, with their findings subsequently verified by a third reviewer. Each reviewer examined the data individually to lead to a consensus while minimizing bias. After extracting data from all included articles, a table was created. This table included the author, publication year, country of origin, number of participants, type of VR used, nature and duration of the intervention, outcome variables and scales used, and results for each study (Table 2) [11,2633].

Characteristics of included studies

Assessment of Study Risk of Bias

The risk of bias in the selected documents was assessed using the Cochrane risk-of-bias tool [34]. The evaluation covered several areas: allocation concealment and random sequence generation (both related to selection bias), blinding of participants and personnel (performance bias), blinding of outcome assessment (detection bias), completeness of outcome data (attrition bias), and selective data reporting (reporting bias) (Table 3) [11,2633]. The level of bias was categorized into 3 grades: low, high, and unclear risk of bias. The reviewers independently assessed the biases in the included studies and, in the event of any discrepancies, consulted a third reviewer for resolution.

Risk of bias assessment

Data Synthesis

We conducted a narrative synthesis of data from the selected studies, encompassing participant characteristics, descriptions of the intervention and control groups, details of the VR interventions, and comparisons between VR and conventional therapy. This synthesis also included assessments of upper limb function and activity, independence in ADLs, and the impact of VR therapy over the course of follow-up.

Results

A total of 589 relevant studies were identified. Of these, 412 were duplicates, 30 did not meet the eligibility criteria, and 112 were excluded after screening titles and abstracts. Ultimately, 35 studies were assessed for eligibility, and 9 RCTs were included in the systematic review.

Study Characteristics

The studies included in this review were conducted in 7 countries: 2 studies in the Republic of Korea [26,27], 2 in China [28,29], 1 in Canada, 1 in Norway [30], 1 in Saudi Arabia [31], 1 in the United Kingdom [32], and 1 in Turkey [33]. The total sample size across the included articles was 558 participants, with 282 in the experimental groups and 276 in the control groups. The time since stroke onset ranged from 9 days to 24 months. Six studies [11,26,2830,33] recruited participants within 6 months after stroke, while 3 trials [27,31,32] included participants for whom more than 6 months had elapsed. In 1 study [32], the intervention and control groups were subdivided into patients with ischemic and hemorrhagic stroke, whereas the other studies did not report specific details about the type of stroke. The frequency of training varied from 3 to 5 sessions per week, and the number of intervention sessions ranged from 10 to 36. The duration of each session varied from 30 minutes to 120 minutes. In 1 study [30], the experimental and control groups were further segmented based on the severity of hand paresis, specifically into mild to moderate hand paresis and severe hand paresis categories. Few studies investigated whether the benefits of VR treatment were sustained in the long term after the therapy concluded. One study [30] reassessed outcomes 3 months post-intervention, while another study [11] conducted an assessment 1 month after the intervention ended.

Risk of Bias and Study Quality

The risk of bias for the included studies is detailed in Table 3 and Figure 1 [11,2633]. All 9 studies employed random sequence generation, allocation concealment, and blinding of outcome assessors. None of the studies exhibited selective reporting or attrition bias, the latter of which pertains to participant dropout. In 7 studies [11,26,27,29,31-33], the participants and personnel were not blinded to the allocated intervention. For the remaining 2 studies [28,30], the risk of performance bias was unclear. Therefore, a high risk of performance bias was found overall, since blinding of participants was not feasible due to the nature of the intervention. Apart from performance bias, all included studies were assessed as having a low risk of bias in all other domains. The outcome assessors were adequately blinded by withholding knowledge of the allocated interventions. Based on the quality assessment of the included studies, the total bias score was determined to be 1 out of 7, indicating a low risk of bias.

Figure 1.

Risk of bias summary for the included trials.

Intervention Group Characteristics

In 7 studies [2628,3133], the intervention group received a combination of conventional treatment and VR therapy, while in 2 studies [29,30] the intervention group was treated exclusively with VR. The VR-based interventions employed in these studies utilized systems that provide feedback within a virtual environment, including You Grabber [30], Armeo Spring [31], VR-based bilateral upper extremity training (VRBT) [27], A2, YiKang, reinforced feedback in a virtual environment (RFVE) [32], a Leap Motion-based VR system [28], and the Interactive Rehabilitation and Exercise? system [26]. Other studies involved the intervention group using commercially available gaming systems for VR-based therapy, such as the Wii (Nintendo) [11] and the Xbox Kinect [33], within a VR environment.

Control Group Characteristics

In 5 studies [11,2932], interventions were administered to both groups with matching frequency (number of sessions per week), session duration, and treatment duration. However, in the remaining 4 studies [2628,33], the duration of therapy for the control group did not match that of the intervention group.

Measurement Tools

A variety of scales were used in the 9 studies to assess improvements in upper limb motor function, arm function, and ADLs. The scales employed included the Fugl-Meyer Assessment-Upper Extremity (FMA-UE) [26,29,32,33], the Box and Block Test (BBT) [11,27,30,33], the Functional Independence Measure (FIM) [11,30,32,33], the Barthel index [11], the Korean version of the modified Barthel index [26], the Action Research Arm Test (ARAT) [2931], the Wolf Motor Function Test (WMFT) [11,28,31], hand grip strength [31], the Grooved Pegboard Test [27], the Jebsen–Taylor Hand Function Test [27], the Brunnstrom stage scale [33], the Stroke Impact Scale (SIS) [11], the Edmonton Symptom Assessment System (ESAS) [32], the Manual Function Test [26], and a dynamometer [11].

Comparison of VR Therapy versus Conventional Therapy/Standard Care/Recreational Therapy

The results of this comparison are detailed in the following sections.

Upper limb function and activity

Upper limb function and activity were assessed in all studies. Of the 9 articles, 5 [27,28,3133] concluded that the stroke survivors receiving VR treatment experienced better outcomes than those administered conventional treatment. One study [29] reported that VR-supported exercises alone were superior to conventional therapy, while 3 studies [11,26,30] indicated that VR training was as effective as conventional methods.

A study by Ikbali Afsar et al. [33] reported better outcomes in the interventional group, with significant differences observed between the experimental and control groups in terms of FMA-UE and BBT scores (p<0.05). Similarly, Wang et al. [28] concluded that the motor function of the affected upper limbs, as measured with the WMFT scale, was significantly improved in the experimental group compared to the control group (p<0.01). Additionally, the WMFT time was significantly shorter in the experimental group (3.29±0.82 seconds) than in the control group (4.24±0.57 seconds) post-intervention. El-Kafy et al. [31] found comparable results, stating that patients in the experimental group showed more favorable improvement than those in the control group in terms of the ARAT (p<0.01), WMFT (p<0.01), and WMFT-Time (p<0.01) assessments. They concluded that the use of combined therapy (VR and conventional rehabilitation) provides greater benefits to upper limb function than conventional treatment alone. Kiper et al. [32] also reported that the experimental group demonstrated better improvement on the FMA-UE scale (p<0.001), FIM (p<0.001), National Institutes of Health Stroke Scale (p≤0.014), and ESAS (p≤0.022) compared to the control group. Kiper et al. [32] further assessed kinetic parameters such as time (p<0.001), speed (p<0.001), and peak (p<0.001) during the execution of the requested task, finding significant differences compared to control participants. Lee et al. [27] reported that members of the VRBT group exhibited significant improvements in upper extremity function and muscle strength (p<0.05). Lastly, Chen et al. [29] described a significant improvement in the ARAT (Z=2.088, p=0.04) and FMA-UE (Z=−2.338, p=0.02) scales in the VR group compared to the control group.

Three studies reported nonsignificant results [11,26,30]. Kwon et al. [26] observed improvements in both groups post-intervention, and the difference between them was not statistically significant (p>0.05). The effect size of the change in the examined variable was medium (Cohen d=0.48) for the FMA. Similarly, Saposnik et al. [11] found that the WMFT performance time improved from baseline to post-intervention for both groups. Specifically, they observed a decrease in the median time from 43.7 seconds (interquartile range [IQR], 26.1–68.0 seconds) to 29.7 seconds (IQR, 21.4–45.2 seconds), representing a 32.0% reduction, for the VRWii group, compared to a change from 38.0 seconds (IQR, 28.0–64.1 seconds) to 27.1 seconds (IQR, 21.2–45.5 seconds), representing a 28.7% reduction, for the patients treated with recreational activity. However, they noted no significant difference in hand function (p=0.314), grip strength (p=0.713), or motor performance (p=0.469) between the groups at the end of the intervention, except for gross manual hand dexterity as measured by the BBT scale (p=0.018). Brunner et al. [30] reported that participants in the VR group improved on the ARAT by 12 points (standard deviation [SD], 11) from baseline to the post-intervention assessment, while the patients receiving conventional therapy improved by 13 points (SD, 10), with no significant difference (p=0.714) between the control and experimental groups.

Independence in daily living

Of the included studies, 5 [11,26,30,32,33] analyzed the impact of VR therapy versus conventional therapy on ADLs. Four of these studies [11,26,30,33] reported no significant differences in ADL performance between the control and experimental groups. Supporting this, Ikbali et al. [33] found no statistical difference (p=0.677) between the groups with regard to FIM score, although both the experimental (12.74±2.51 to 23.74±4.42) and control (13.63±3.61 to 23.63±4.99) groups showed improvement from baseline to post-intervention. Kwon et al. [26] also reported no significant difference in ADL between the VR and conventional therapy groups (p>0.05), despite a large effect size (Cohen d=1.02). Saposnik et al. [11] observed similar improvements in the Barthel index in the experimental (64.7±22.4 to 83.4±18.0) and control (64.2±23.0 to 80.3±21.7) groups. Brunner et al. [30] noted comparable improvements in FIM motor scores in the VR group (changing from 15.9 at baseline to 12.7 after intervention) and the conventional therapy group (changing from 17.5 at baseline to 13.1 after intervention) post-intervention and at follow-up. However, Kiper et al. [32] reported a significant improvement in independence in daily living associated with VR therapy, as measured with FIM (RFVE, 8.42%; conventional rehabilitation, 4.82%; p<0.001).

Upper limb function: follow-up

Only 2 studies [11,30] analyzed the long-term benefits of VR therapy among patients treated after stroke. Brunner et al. [30] observed an improvement in upper extremity function as assessed with ARAT, with a mean increase of 17 points (SD, 13) from baseline to follow-up in the VR group, which was identical to the improvement seen in the conventional therapy group. Consequently, no significant difference was found (p=0.777) between groups at follow-up when assessing all scales (ARAT, BBT, FIM, and Patient Global Impression of Change). Similarly, Saposnik et al. [11] found no significant differences at the 4-week post-intervention mark in WMFT performance time (p=0.346), Barthel index (p=0.774), FIM (p=0.848), or SIS hand function (p=0.514) between the control group (who engaged in recreational activity) and the experimental group (who received VRWii therapy).

Discussion

More than three-quarters of stroke victims experience diminished upper limb function following the event, impacting their everyday quality of life. The aim of this study was to compare motor recovery of upper limb function between interventional (VR therapy) and control (conventional therapy) groups. The interventional group received both conventional treatment and VR therapy in 7 studies [2628,3133], while only VR therapy was administered in 2 studies [29,30].

Of the 9 studies examined, 5 [27,28,3133] concluded that the VR treatment group of stroke survivors experienced better outcomes than those who received conventional treatment. One study [29] reported the superiority of VR-supported exercises, while 3 studies [11,26,30] found that VR training was similarly effective to conventional methods. Most of the included studies [2729,3133] noted that the intervention group experienced greater improvements in upper limb function and activity than the control group. According to El-Kafy et al. [31], interventional groups using combination therapy (both virtual and traditional) saw greater enhancements in upper limb function. All trials considered reported a similar degree of improvement in ADLs between groups. Vinas-Diz and Sobrido-Prieto [35] have emphasized that VR can create environments specifically tailored for patients by modifying and controlling their engagement with their surroundings, potentially serving as a valuable adjunct or alternative to conventional therapy. In a separate comprehensive review, Zhu et al. [36] found that VR intervention is a beneficial non-pharmacological approach for enhancing cognitive and motor performance in older individuals. Wiley et al. [37] observed that the VR group performed better than the control when VR was used as an add-on to conventional therapy, concluding that VR therapy is stimulating and interesting relative to traditional rehabilitation methods. These findings aligned with those of several included studies [27,28,3133]. Zhang et al. [38] also reported that the upper limb function in the VR group outperformed that of the conventional method, with significant differences found between the 2 groups regardless of the intervention period. This was consistent with results from other included studies [27,28,3133], which had varied intervention durations. Separately, Zhu et al. [36] concluded that VR treatment is beneficial for improving outcomes in patients with mild cognitive impairment after stroke. A systematic review by Gao et al. [39] concluded that VR-based training did not have significant benefits over conventional methods on motor function or ADLs. However, they suggested that greater duration, frequency, and daily intensity of VR training may yield better outcomes. Chen et al. [29] reported that although the VR group showed significant improvement in upper extremity motor function and independence in day-to-day activities, the results were inconclusive regarding the benefits of VR therapy after the intervention ended. This was consistent with findings from other included studies [11,30]. The strengths of this systematic review include the exclusive inclusion of RCTs and a rigorous quality assessment of included studies using the Cochrane risk-of-bias tool. This review highlights several opportunities for future research to evaluate the long-term benefits of VR-supported exercises. However, several limitations should be addressed. Most of the included studies had small sample sizes, which limited generalizability and weakened the validity of the results. Secondly, the intervention type (immersive or non-immersive VR), duration, and frequency varied between studies, potentially influencing rehabilitation progress. The optimal frequency and duration of intervention remain to be explored.

Implications for Practice

VR-based interventions can be incorporated into clinical practice to rehabilitate the upper limb in conjunction with conventional exercises. Commercially available games, such as Nintendo Wii Sports, are readily accessible and affordable, making them a potentially appealing choice. Specialized VR programs can also be tailored to the patient’s condition, enabling clinicians to effectively integrate VR treatment for rehabilitation after stroke.

Recommendations

The optimal frequency and duration of intervention using VR have yet to be determined, necessitating further research to compare the impacts of various VR interventions, including their respective frequencies and durations. Moreover, a need exists for studies with larger sample sizes to evaluate the long-term effects of VR-supported exercises. Additionally, the suitability of these interventions following stroke warrants further investigation to ascertain which patient groups are most likely to benefit and to determine the optimal timing for initiating intervention across the stages of stroke recovery (acute, subacute, and chronic). Research should also be conducted to examine the potential adverse effects associated with VR-supported exercises.

Conclusion

Most studies included in this review suggest that incorporating VR-supported exercise alongside conventional therapy may enhance the improvement of upper limb function and activity. However, the long-term benefits of VR-supported exercises among patients after stroke remain inconclusive.

HIGHLIGHTS

• Healthcare providers can integrate virtual reality (VR)-supported exercises into rehabilitation programs for survivors of stroke.

• The use of VR as a supplement to conventional therapy shows promise as an adjuvant for this patient population.

Figure 2.

Risk of bias graph.

Figure 3.

PRISMA flowchart for the selection of articles for integrative review.

PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analyses; RCT, randomized controlled trial; VR, virtual reality.

Supplementary Material

Supplementary data are available at https://doi.org/10.24171/j.phrp.2023.0148.

Supplementary Material 1.

Preferred Reporting Items for Systematic Reviews and Meta-Analyses 2020 checklist.

j-phrp-2023-0148-Supplementary-Material-1.pdf

Notes

Ethics Approval

Not applicable.

Conflicts of Interest

The authors have no conflicts of interest to declare.

Funding

None.

Availability of Data

The datasets used in this study are not publicly accessible; however, they can be obtained from the corresponding author upon reasonable request.

Authors’ Contributions

Conceptualization: PD, UP; Data curation: PD, SPS; Formal analysis: PD, NK; Investigation: UP; Methodology: PD, SPS; Project administration: NK, PD; Software: PD, NK; Supervision: NK; Validation: UP; Visualization: PD; Writing–original draft: PD, UP, NK; Writing–review & editing: all authors. All authors read and approved the final manuscript.

References

1. Lopez AD, Mathers CD, Ezzati M, et al. Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data. Lancet 2006;367:1747–57.
2. Warlow CP. Epidemiology of stroke. Lancet 1998;352 Suppl 3:SIII1–4.
3. Sacco RL, Kasner SE, Broderick JP, et al. An updated definition of stroke for the 21st century: a statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 2013;44:2064–89.
4. Mayo NE, Wood-Dauphinee S, Ahmed S, et al. Disablement following stroke. Disabil Rehabil 1999;21:258–68.
5. Skold A, Josephsson S, Eliasson AC. Performing bimanual activities: the experiences of young persons with hemiplegic cerebral palsy. Am J Occup Ther 2004;58:416–25.
6. Intercollegiate Stroke Working Party. National clinical guideline for stroke 4th edth ed. Royal College of Physicians; 2012.
7. Buma FE, Lindeman E, Ramsey NF, et al. Functional neuroimaging studies of early upper limb recovery after stroke: a systematic review of the literature. Neurorehabil Neural Repair 2010;24:589–608.
8. Kwakkel G, Veerbeek JM, van Wegen EE, et al. Constraint-induced movement therapy after stroke. Lancet Neurol 2015;14:224–34.
9. Wiklund LM, Uvebrant P. Hemiplegic cerebral palsy: correlation between CT morphology and clinical findings. Dev Med Child Neurol 1991;33:512–23.
10. Chin LF, Hayward KS, Brauer S. Upper limb use differs among people with varied upper limb impairment levels early post-stroke: a single-site, cross-sectional, observational study. Top Stroke Rehabil 2020;27:224–35.
11. Saposnik G, Cohen LG, Mamdani M, et al. Efficacy and safety of non-immersive virtual reality exercising in stroke rehabilitation (EVREST): a randomised, multicentre, single-blind, controlled trial. Lancet Neurol 2016;15:1019–27.
12. Teasell R, Meyer MJ, McClure A, et al. Stroke rehabilitation: an international perspective. Top Stroke Rehabil 2009;16:44–56.
13. Weiss PL, Katz N. The potential of virtual reality for rehabilitation. J Rehabil Res Dev 2004;41:vii–x.
14. Maier M, Rubio Ballester B, Duff A, et al. Effect of specific over nonspecific VR-based rehabilitation on poststroke motor recovery: a systematic meta-analysis. Neurorehabil Neural Repair 2019;33:112–29.
15. Sanchez-Vives MV, Slater M. From presence to consciousness through virtual reality. Nat Rev Neurosci 2005;6:332–9.
16. Reid D, Campbell K. The use of virtual reality with children with cerebral palsy: a pilot randomized trial. Ther Recreation J 2006;40
17. Burdea GC. Virtual rehabilitation: benefits and challenges. Methods Inf Med 2003;42:519–23.
18. Huang X, Naghdy F, Naghdy G, et al. Clinical effectiveness of combined virtual reality and robot assisted fine hand motion rehabilitation in subacute stroke patients. IEEE Int Conf Rehabil Robot 2017;2017:511–5.
19. Connelly L, Jia Y, Toro ML, et al. A pneumatic glove and immersive virtual reality environment for hand rehabilitative training after stroke. IEEE Trans Neural Syst Rehabil Eng 2010;18:551–9.
20. Jang SH, You SH, Hallett M, et al. Cortical reorganization and associated functional motor recovery after virtual reality in patients with chronic stroke: an experimenter-blind preliminary study. Arch Phys Med Rehabil 2005;86:2218–23.
21. Merians AS, Poizner H, Boian R, et al. Sensorimotor training in a virtual reality environment: does it improve functional recovery poststroke? Neurorehabil Neural Repair 2006;20:252–67.
22. Piron L, Tonin P, Atzori AM, et al. The augmented-feedback rehabilitation technique facilitates the arm motor recovery in patients after a recent stroke. Stud Health Technol Inform 2003;94:265–7.
23. Yavuzer G, Senel A, Atay MB, et al. “Playstation eyetoy games” improve upper extremity-related motor functioning in subacute stroke: a randomized controlled clinical trial. Eur J Phys Rehabil Med 2008;44:237–44.
24. Yong Joo L, Soon Yin T, Xu D, et al. A feasibility study using interactive commercial off-the-shelf computer gaming in upper limb rehabilitation in patients after stroke. J Rehabil Med 2010;42:437–41.
25. Laver KE, George S, Thomas S, et al. Virtual reality for stroke rehabilitation. Cochrane Database Syst Rev 2015;2015:CD008349.
26. Kwon JS, Park MJ, Yoon IJ, et al. Effects of virtual reality on upper extremity function and activities of daily living performance in acute stroke: a double-blind randomized clinical trial. NeuroRehabilitation 2012;31:379–85.
27. Lee S, Kim Y, Lee BH. Effect of virtual reality-based bilateral upper extremity training on upper extremity function after stroke: a randomized controlled clinical trial. Occup Ther Int 2016;23:357–68.
28. Wang ZR, Wang P, Xing L, et al. Leap Motion-based virtual reality training for improving motor functional recovery of upper limbs and neural reorganization in subacute stroke patients. Neural Regen Res 2017;12:1823–31.
29. Chen L, Chen Y, Fu WB, et al. The effect of virtual reality on motor anticipation and hand function in patients with subacute stroke: a randomized trial on movement-related potential. Neural Plast 2022;2022:7399995.
30. Brunner I, Skouen JS, Hofstad H, et al. Virtual Reality Training for Upper Extremity in Subacute Stroke (VIRTUES): a multicenter RCT. Neurology 2017;89:2413–21.
31. El-Kafy EM, Alshehri MA, El-Fiky AA, et al. The effect of virtual reality-based therapy on improving upper limb functions in individuals with stroke: a randomized control trial. Front Aging Neurosci 2021;13:731343.
32. Kiper P, Szczudlik A, Agostini M, et al. Virtual reality for upper limb rehabilitation in subacute and chronic stroke: a randomized controlled trial. Arch Phys Med Rehabil 2018;99:834–42.
33. Ikbali Afsar S, Mirzayev I, Umit Yemisci O, et al. Virtual reality in upper extremity rehabilitation of stroke patients: a randomized controlled trial. J Stroke Cerebrovasc Dis 2018;27:3473–8.
34. Higgins JP, Altman DG, Gotzsche PC, et al. The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials. BMJ 2011;343:d5928.
35. Vinas-Diz S, Sobrido-Prieto M. Virtual reality for therapeutic purposes in stroke: a systematic review. Neurologia 2016;31:255–77.
36. Zhu S, Sui Y, Shen Y, et al. Effects of virtual reality intervention on cognition and motor function in older adults with mild cognitive impairment or dementia: a systematic review and meta-analysis. Front Aging Neurosci 2021;13:586999.
37. Wiley E, Khattab S, Tang A. Examining the effect of virtual reality therapy on cognition post-stroke: a systematic review and meta-analysis. Disabil Rehabil Assist Technol 2022;17:50–60.
38. Zhang B, Wong KP, Qin J. Effects of virtual reality on the limb motor function, balance, gait, and daily function of patients with stroke: systematic review. Medicina (Kaunas) 2023;59:813.
39. Gao Y, Ma L, Lin C, et al. Effects of virtual reality-based intervention on cognition, motor function, mood, and activities of daily living in patients with chronic stroke: a systematic review and meta-analysis of randomized controlled trials. Front Aging Neurosci 2021;13:766525.

Article information Continued

Figure 1.

Risk of bias summary for the included trials.

Figure 2.

Risk of bias graph.

Figure 3.

PRISMA flowchart for the selection of articles for integrative review.

PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analyses; RCT, randomized controlled trial; VR, virtual reality.

Table 1.

PICOTS criteria for included studies

Criteria
Population Patients with a maximum of 2 years elapsed since stroke
Intervention Virtual reality treatment (immersive or non-immersive)
Comparators Conventional techniques/recreational activity/standard treatment
Outcome Upper limb function and activity
Time Published in the last 10 years
Study design Randomized controlled trial

Table 2.

Characteristics of included studies

No. Study Year Country Time elapsed since stroke Participant (n) Type of VR Intervention Duration of intervention Outcome variables and scales Results
1 Saposnik et al. [11] 2016 Canada Within 3 mo of enrollment 121 (VR: 59, control: 62) Non-immersive Experimental group: VR treatment 10 sessions×60 min/session over 2 wk UE-motor function: WMFT, BBT, FIM, SIS, Barthel index, dynamometer No significant difference was found between the VR and recreational therapy group on FM, FIM, SIS, Barthel index, or grip strength in the post-intervention and follow-up period. Regarding ADL, similar improvement was observed between the groups.
Control group: recreational activity (playing cards, bingo, etc.)
2 Brunner et al. [30] 2017 Norway Within 3 mo of stroke 120 (VR: 62, control: 58) Non-immersive Experimental group: VR training+standard rehabilitation 16 sessions×60 min/session over 4 wk in both groups UE-motor function: ARAT No significant difference was noticed between the 2 groups (p=0.714) in motor function improvement or ADL (p=0.777).
Control group: conventional training+standard rehabilitation Dexterity assessment: BBT Regarding ADL, both groups showed similar improvement, representing a nonsignificant difference (p=0.777).
Independence in ADL: FIM
3 Kiper et al. [32] 2018 United Kingdom 12 mo 136 (VR: 68, control: 68) Non-immersive Experimental group: 1 h of CR and 1 h of RFVE 2 h session/d×5 d/wk×4 wk UE-motor function: FMA-UE RFVE therapy combined with CR treatment promotes better upper limb outcomes on the FMA-UE scale (p<0.001), NIHSS (p≤0.014), and ESAS (p≤0.022) compared to CR.
Control group: r2 hours of CR ADL: FIM Regarding ADL, a significant difference was also found on the FIM (p<0.001) scale.
4 Chen et al. [29] 2022 China 1–3 mo 36 (VR: 18, control: 18) Non-immersive Experimental group: VR training 60 min×5 sessions/wk×2 wk UE-motor function: ARAT, FMA-UE The improvement in ARAT and FMA-UE in the VR group was significantly higher than in the control group.
Control group: conventional therapy
5 Ikbali Afsar et al. [33] 2018 Turkey 1–6 mo 35 (VR: 19, control: 16) Non-immersive Experimental group: conventional therapy+VR therapy (Xbox Kinect game system) CT: 60 min session/d×5 d/wk×4 wk UE-motor function: FMA-UE, Gross manual dexterity: BBT, ADL: FIM A significant difference was found between groups in both BBT score and FMA-UE (p<0.05).
Control group: conventional rehabilitation only VR therapy: 30 min/d Regarding ADL, no significant difference was observed (p=0.677).
6 Lee et al. [27] 2016 Republic of Korea Diagnosis of stroke at least 6 mo prior 18 (VRBT group: 10; bilateral training group: 8) Non-immersive Experimental group: bilateral upper extremity exercises in a VR environment in addition to CT Control group: bilateral upper extremity exercises while watching irrelevant videos in addition to CT VR-based bilateral training: 30 min session/d × 3 d/wk × 6 wk UE-motor function: JHFT, BBT, GPT The VRBT group exhibited significant improvement in upper extremity function and muscle strength (p<0.05).
Control group: bilateral upper extremity exercises while watching irrelevant videos in addition to CT Conventional therapy: 30 min session/d × 3 d/wk × 6 wk Muscle strength: DMMT
7 Wang et al. [28] 2017 China 4 wk–6 mo 26 (VR: 13, control: 13) Immersive Experimental group: Leap Motion VR+conventional treatment Experimental group: Leap Motion VR: once a day (45 min), 5 d/wk for 4 wk + CT: once a day (45 min), 5 d/wk for 4 wk UE-motor function: WMFT A significant difference was found between the control and experimental groups in WMFT-Time (p<0.01).
Control group: conventional therapy (stretches, strength, balance, gait training) Control group: twice a day each 45 min, 5 d/wk for 4 wk
8 Kwon et al. [26] 2012 Republic of Korea Within 3 mo of the stroke 26 (VR: 13, control: 13) Immersive Experimental group: VR therapy in addition to CT VR therapy: 30 min/d×5 d/wk×4 wk UE-motor function: FMA, MFT The VR group showed improvement in both FMA and MFT scores. In the CT group, only the FMA score improved.
Control group: CT only Conventional therapy: 70 min/d×5 d/wk×4 wk Independence in ADL: K-MBI K-MBI (ADL performance) improved in both groups, with no significant differences observed in upper extremity function or ADL performance (p>0.05).
9 El-Kafy et al. [31] 2021 Saudi Arabia 6–24 mo 40 (VR: 20, control: 20) Non-immersive Experimental group: 1 h CT+1 h VR therapy 2 h session×3 sessions/wk×3 mo UE-motor function: WMFT, ARAT The experimental group displayed greater improvement in all measured scales (ARAT, WMFT, and WMFT-Time) compared to the control group.
Control group: 2 h CT

VR, virtual reality; UE, upper extremity; CR, conventional rehabilitation; CT, conventional therapy; ADL, activities of daily living; BBT, Box and Block Test; FIM, Functional Independence Measure; ARAT, Action Research Arm Test; FMA-UE, Fugl-Meyer Assessment-Upper Extremity; NIHSS, National Institutes of Health Stroke Scale; WMFT, Wolf Motor Function Test; JHFT, Jebsen–Taylor Hand Function Test; GPT, Grooved Pegboard Test; DMMT, Digital Manual Muscle Test; MFT, Manual Function Test; K-MBI, Korean version of the modified Barthel index; SIS, Stroke Impact Scale; ESAS, Edmonton Symptom Assessment System; RFVE, reinforced feedback in a virtual environment; VRBT, virtual reality-based bilateral upper extremity training.

Table 3.

Risk of bias assessment

Study Year Random sequence generation Allocation concealment Blinding of participants and personnel Blinding of outcome assessment Incomplete outcome data Selective reporting bias Other, ideally specified
Saposnik et al. [11] 2016 Low risk Low risk High risk Low risk Low risk Low risk Low risk
Brunner et al. [30] 2017 Low risk Low risk Unclear risk Low risk Low risk Low risk Low risk
Kiper et al. [32] 2018 Low risk Low risk High risk Low risk Low risk Low risk Low risk
Chen et al. [29] 2022 Low risk Low risk High risk Low risk Low risk Low risk Low risk
Ikbali Afsar et al. [33] 2018 Low risk Low risk High risk Low risk Low risk Low risk Low risk
Lee et al. [27] 2014 Low risk Low risk High risk Low risk Low risk Low risk Low risk
Wang et al. [28] 2017 Low risk Low risk Unclear risk Low risk Low risk Low risk Low risk
Kwon et al. [26] 2012 Low risk Low risk High risk Low risk Low risk Low risk Low risk
El-Kafy et al. [31] 2021 Low risk Low risk High risk Low risk Low risk Low risk Low risk