Skip to main content

SYSTEMATIC REVIEW article

Front. Neurol., 27 August 2024
Sec. Neurorehabilitation
This article is part of the Research Topic Exploring Evidence for Neurorehabilitation Advancements View all 23 articles

Effects of body weight support training on balance and walking function in stroke patients: a systematic review and meta-analysis

Zhaoxiang Jiang,&#x;Zhaoxiang Jiang1,2Xinxin Zhang&#x;Xinxin Zhang1Qian FuQian Fu1Yimin Tao
Yimin Tao3*
  • 1College of Physical Education and Health, Guangxi Normal University, Guilin, China
  • 2School of Sports Economics and Management, Guangxi University of Finance and Economics, Nanning, China
  • 3Guilin University of Aerospace Technology, Guilin, China

Objective: To comprehensively and quantitatively evaluate the impact of body weight support training (BWST) on balance and gait function in stroke patients based on an evidence-based basis and to identify the most effective intervention strategies.

Methods: PubMed, Web of Science, The Cochrane Library, CNKI, Wanfang, and Chinese SinoMed Database were searched until November 25, 2023. Quality assessment and meta-analysis were performed using RevMan 5.2 and Stata 14.0 software.

Results: A total of 31 randomized controlled trials involving 1,918 patients were included in the study. The meta-analysis demonstrated that body weight support training (BWST) significantly improved Berg Balance Scale (BBS) scores (MD = 3.60; 95% CI: 1.23 to 5.98; p = 0.003), gait speed (SMD = 0.77; 95% CI: 0.38 to 1.15; p < 0.0001), and step length (SMD = 0.46; 95% CI: 0.19 to 0.72; p = 0.0008) in stroke patients compared to conventional rehabilitation. For enhancing balance function, the most effective interventions were identified as a disease duration of 3–6 months (MD = 5.16; 95% CI: 0.76 to 9.57; p = 0.02), intervention time of 4–8 weeks (MD = 5.70; 95% CI: 2.90 to 8.50; p < 0.0001), a maximum body weight support level above 30% (MD = 3.80; 95% CI: 1.48 to 6.13; p = 0.001), and a maximum training walking speed of 0.2 m/s or more (MD = 4.66; 95% CI: 0.37 to 9.70; p = 0.03). For improving walking function, the optimal interventions were also a disease duration of 3–6 months (gait speed: SMD = 0.59; 95% CI: 0.15 to 1.03; p = 0.008; step length: SMD = 0.27; 95% CI: 0.06 to 0.56; p = 0.04), intervention time of 4–8 weeks (gait speed: SMD = 1.01; 95% CI: 0.44 to 1.59; p = 0.0006; step length: SMD = 0.83; 95% CI: 0.54 to 1.12; p < 0.00001), a maximum body weight support level above 30% (gait speed: SMD = 0.79; 95% CI: 0.36 to 1.22; p = 0.0003; step length: SMD = 0.79; 95% CI: 0.47 to 1.11; p < 0.00001), and a maximum training walking speed of 0.2 m/s or more (gait speed: SMD = 1.26; 95% CI: 0.62 to 1.90; p = 0.0001; step length: SMD = 0.85; 95% CI: 0.38 to 1.31; p = 0.0003).

Conclusion: Compared with conventional rehabilitation training, BWST demonstrates superior efficacy in enhancing balance and walking function in stroke patients, with a consistent optimal intervention strategy. The most effective program includes a disease duration of 3–6 months, an intervention period of 4–8 weeks, a maximum body weight support of 30% or more, and a maximum training walking speed of 0.2 m/s or greater.

Systematic review registration: http://www.crd.york.ac.uk/PROSPERO/, identifier: CRD42022358963.

Introduction

Stroke is one of the most prevalent neurological disorders globally. The primary objective of rehabilitation for early-stage stroke patients is to restore lower limb motor function, particularly on balance and walking abilities (1). Previous studies have indicated (1, 2) that over 80% of stroke patients experience balance and walking dysfunction during the acute/subacute phase, characterized by impaired postural alignment, increased sway, asymmetrical gait, and diminished responsiveness to external forces. These impairments significantly reduce patients’ independence and quality of life in performing basic activities of daily living and impose a substantial psychological burden (3, 4). Therefore, finding the best and most effective intervention program for restoring motor function in stroke patients is a key goal for patients (5) and remains a critical scientific issue of significant interest in the field of rehabilitation.

Body weight support training (BWST) is an innovative rehabilitation method that utilizes suspension or pneumatic compression techniques to reduce the effective load of the patient’s body weight during exercise (6). Stroke patients often suffer from overall neurological and motor decline, so their rehabilitation interventions are more demanding than those for single sports injuries (7, 8). BWST is a crucial intervention to reduce weight load, enabling patients to perform comprehensive gait exercises. This approach is better suited to the holistic rehabilitation required by stroke patients than conventional rehabilitation methods and facilitates motor relearning and neural pathway reorganization (9, 10). BWST has been increasingly employed in stroke rehabilitation in recent years, demonstrating notable efficacy (1). A recent study (11) indicated that BWST could significantly enhance lower limb motor function and rehabilitation outcomes, improve patients’ ability to perform daily activities and enhance their quality of life, thereby accelerating their reintegration into family and society. However, previous studies have reported varying results regarding how BWST improves balance and walking function in stroke patients (12, 13). These discrepancies may stem from differences in disease duration and training parameter settings (such as training intensity or intervention time). While earlier research (1419) has examined individual training parameters (e.g., training time, load), these studies were limited by small sample sizes and the specific characteristics of the included patients, resulting in findings with certain limitations. More importantly, previous intervention trials could only investigate the effect of a single intervention element without exploring the combined effects of different aspects from a multidimensional perspective. Consequently, the optimal intervention program remains undefined.

Therefore, this study aimed to adopt an evidence-based medicine approach to comprehensively and quantitatively assess the effects of BWST on balance and walking function in stroke patients through meta-analysis. Additionally, it sought to identify the optimal intervention program, aiming to discover the most effective rehabilitation strategies for stroke patients and provide valuable references for developing exercise prescriptions.

Methods

This review was registered (Identifier: CRD42022358963) in the International Prospective Register of Systematic Reviews (PROSPERO) and complied with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement (20).

Study search and selection

We conducted a comprehensive literature search across PubMed, Web of Science, The Cochrane Library, CNKI, Wanfang, and Chinese SinoMed Databases until November 2023, without any language restrictions. The search terms included (a) Stroke or Cerebral stroke, Cerebral vascular accident or CVA, and (b) Antigravity treadmill or Body weight support. Taking the PubMed database as an example, the specific search strategy is: ((((Stroke [Title/Abstract]) OR (cerebral stroke [Title/Abstract])) OR (cerebral vascular accident [Title/Abstract])) OR (CVA [Title/Abstract])) AND ((antigravity treadmill [Title/Abstract]) OR (body weight support [Title/Abstract])).

The inclusion criteria for this meta-analysis were: (a) the study was a randomized controlled trial, (b) participants were patients with a clinical diagnosis of stroke, (c) interventions involved BWST combined with conventional rehabilitation treatments for the trial group and conventional rehabilitation treatments only for the control group, and (d) the outcomes included Berg Balance Scale (BBS) scores and walking function parameters such as gait speed and step length. The exclusion criteria were: (a) studies that did not involve BWST interventions, (b) interventions that combined BWST with other therapies, (c) patients with other types of diseases, (d) studies with missing or inconsistent outcomes, (e) conference and dissertation papers, and (f) duplicate publications.

EndNote X9 software was used to remove duplicate records from the search results. The title and abstract of retrieved articles were initially read and screened by two reviewers (Z.J., X.Z.) using an independent double-blind approach following the study inclusion and exclusion criteria. Articles that might meet the inclusion criteria were downloaded in full text and read for re-screening to finalize the article’s inclusion. For articles with divergent extractions by two reviewers, a third reviewer (Y.T.) was added to decide on inclusion through joint discussion.

Data extraction and quality assessment

Two reviewers (Z.J. and X.Z.) independently extracted data from the included articles using a pre-designed form. The extracted information primarily included: (1) basic information about the article, such as the first author and year of publication; (2) basic information about the trial participants, including sample size, age, and disease duration; (3) details of the trial intervention, such as intervention time, frequency, degree of body weight support, and training speed; and (4) baseline and endpoint data of the outcomes.

The risk of bias for the included articles was assessed using the Cochrane Collaboration’s risk-of-bias guidelines (21). This evaluation covered seven key areas: (1) random sequence generation, (2) allocation concealment, (3) blinding of participants and personnel, (4) blinding of outcome assessments, (5) incomplete outcome data, (6) selective reporting, and (7) other biases. Two reviewers (X.Z. and Q.F.) conducted the quality assessment independently. In cases of disagreement, a third reviewer (Y.T.) was involved to reach a consensus through discussion.

Data synthesis and statistical analysis

Forest plots and subgroup analyses were conducted using RevMan 5.2 software, while funnel plots, sensitivity analyses, meta-regression, and publication bias tests (Egger’s method) were performed using Stata 14.0 software. Effect sizes were reported as mean ± standard deviation with 95% Confidence Intervals (95% CI). Mean Difference (MD) was used for outcomes measured in the same units, while Standardized Mean Difference (SMD) was used for outcomes in different units (22). The Chi2 test and I2 statistic were used to assess study heterogeneity, with analyses conducted using RevMan 5.2 and Stata 14.0 software. A fixed-effects model was applied if heterogeneity was not statistically significant (I2 < 50%; p > 0.05); otherwise, a random-effects model was employed (23). Sensitivity analyses were conducted for outcomes with heterogeneity to evaluate the stability of findings, and meta-regression analyses were used to explore sources of heterogeneity. Based on study characteristics, subgroup analyses assessed moderating variables that might influence effect sizes. Statistical significance was set at α = 0.05, with p < 0.05 indicating significance.

Results

Search results

A total of 712 records were retrieved. After removing duplicates using EndNote, 556 records remained for initial screening. After reviewing titles and abstracts, 463 articles were excluded for irrelevance. The remaining 93 studies were then re-screened through full-text review, excluding 62 studies that did not meet the inclusion criteria. Ultimately, 31 studies were included in the meta-analysis (1, 1113, 19, 2449). The literature screening process is depicted in Figure 1.

Figure 1
www.frontiersin.org

Figure 1. The flow diagram of the selection process.

Methodological quality assessment

The 31 studies in the meta-analysis involved 1,918 participants, with basic study information detailed in Table 1. The quality of the included studies was assessed using the Cochrane Risk of Bias Assessment Tool. Studies were classified as having a low risk of bias if all seven aspects were evaluated as “low risk.” If one or two aspects were rated as “high risk” or “uncertain risk,” the study was considered to have a moderate risk of bias. Studies with more than two aspects rated as “high risk” or “uncertain risk” were classified as having a high risk of bias. Based on this, six studies were evaluated as low risk of bias (12, 29, 32, 43, 45, 48), four studies were evaluated as moderate risk of bias (11, 19, 42, 44), and 21 studies were evaluated as high risk of bias (1, 13, 2428, 30, 31, 3341, 46, 47, 49). All studies had a low risk of incomplete outcome data and selective reporting and a high risk of random sequence generation. The evaluation results are shown in Figure 2.

Table 1
www.frontiersin.org

Table 1. The detailed characteristics of each included study.

Figure 2
www.frontiersin.org

Figure 2. Results of quality evaluation of included studies.

Meta-analytic results

Effect of BWST on BBS scores

Twenty-two of the 31 included studies (1, 19, 2426, 2935, 37, 38, 40, 42, 4449) were analyzed for BBS scores. Due to high heterogeneity among the combined results (I2 = 98%), a random effects model was employed for the meta-analysis. The combined effect size indicated a significant improvement in BBS scores in the BWST group compared to the control group (MD = 3.60; 95% CI: 1.23–5.98; p = 0.003). The results are presented in Figure 3.

Figure 3
www.frontiersin.org

Figure 3. Effects of BWST on BBS scores.

To investigate the effects of relevant moderating variables on the results of the study, four moderating variables were extracted based on the characteristics of the included studies, namely, patients’ disease duration, intervention time, maximum degree of body weight support, and maximum training gait speed. A subgroup analysis based on the above moderating variables found (as shown in Table 2) that the intervention was most effective for patients with a disease duration of 3–6 months (MD = 5.16; 95% CI: 0.76 to 9.57; p = 0.02). No statistically significant effects were observed for patients with a disease duration of 1–3 months (MD = 4.78; 95% CI: −1.80 to 11.36; p = 0.15) or more than 6 months (MD = 0.04; 95% CI: −0.32 to 0.40; p = 0.82). The most effective treatment was observed with an intervention duration of 4–8 weeks (MD = 5.70; 95% CI: 2.90–8.50; p < 0.0001). Interventions lasting 1–4 weeks (MD = −0.04; 95% CI: −3.28 to 3.19; p = 0.98) or more than 8 weeks (MD = 6.32; 95% CI: −2.61 to 15.26; p = 0.17) showed no statistically significant effect. An intervention with a maximum body weight support of 30% or more was effective (MD = 3.80; 95% CI: 1.48–6.13; p = 0.001). Support of 0–30% did not show a statistically significant treatment effect (MD = 1.34; 95% CI: −4.04 to 6.73; p = 0.62). A maximum training gait speed of 0.2 m/s or more significantly improved balance function (MD = 4.66; 95% CI: 0.37–9.70; p = 0.03), while speeds of 0–0.2 m/s did not show a statistically significant effect (MD = 2.96; 95% CI: −0.83 to 6.75; p = 0.13). In conclusion, BWST was most effective in improving BBS scores in stroke patients with a disease duration of 3–6 months, an intervention time of 4–8 weeks, a maximum body weight support of 30% or more, and a maximum training gait speed of 0.2 m/s or more.

Table 2
www.frontiersin.org

Table 2. Subgroup analysis of moderating variables affecting BBS scores.

Additionally, meta-regression analysis was conducted to identify significant factors influencing heterogeneity when the number of studies exceeded ten and the heterogeneity I2 was >50%. The results (shown in Table 3) indicated that intervention time (p = 0.319), maximum body weight support (p = 0.302), and maximum training gait speed (p = 0.441) did not significantly contribute to heterogeneity. In contrast, disease duration showed a statistically significant result (p = 0.046), suggesting it may be the primary source of heterogeneity.

Table 3
www.frontiersin.org

Table 3. Meta-regression analysis of different moderating variables on BBS scores.

Effect of BWST on walking function

A total of 14 (1113, 19, 2428, 36, 41, 43, 44, 49) of the 31 included studies analyzed gait speed. Due to significant heterogeneity among the results (I2 = 87%), a random effects model was employed for the meta-analysis. The combined effect size demonstrated a significantly greater gait speed in the BWST group than in the control group (SMD = 0.77; 95% CI: 0.38 to 1.15; p < 0.0001, Figure 4). Additionally, 10 (11, 13, 19, 26, 27, 36, 38, 41, 43, 49) of the 31 studies included analyzed step length. Given the large heterogeneity in the combined results (I2 = 58%), a random effects model was also used for the meta-analysis. The combined effect size revealed a significantly greater improvement in step length for the BWST group compared to the control group (SMD = 0.46; 95% CI: 0.19–0.72; p = 0.0008, Figure 5).

Figure 4
www.frontiersin.org

Figure 4. Effect of BWST on gait speed.

Figure 5
www.frontiersin.org

Figure 5. Effect of BWST on step length.

Also, subgroup analyses were conducted to explore the impact of relevant moderating variables—disease duration, intervention time, maximum degree of body weight support, and maximum training gait speed—on study outcomes (Table 4). It was found that in terms of the gait speed outcome, the intervention was most effective for patients with a disease duration of 3–6 months (SMD = 0.59; 95% CI: 0.15–1.03; p = 0.008). No significant effects were observed for durations of 1–3 months (SMD = 0.57; 95% CI: −0.07 to 1.22; p = 0.08) or more than 6 months (SMD = 0.32; 95% CI: −0.31 to 0.96; p = 0.32). An intervention time of 4–8 weeks showed superior results (SMD = 1.01; 95% CI: 0.44–1.59; p = 0.0006) compared to 1–4 weeks (SMD = 0.53; 95% CI: 0.12–0.93; p = 0.01). An intervention duration of more than 8 weeks (SMD = 1.18; 95% CI: −0.01 to 2.37; p = 0.05) was not statistically significant. Maximum body weight support of 30% or more was more effective (SMD = 0.79; 95% CI: 0.36–1.22; p = 0.0003) than support of 0–30% (SMD = 0.67; 95% CI: 0.29–1.05; p < 0.00001). A maximum gait speed of 0.2 m/s or more resulted in better outcomes (SMD = 1.26; 95% CI: 0.62–1.90; p = 0.0001) compared to speeds of 0–0.2 m/s (SMD = 0.60; 95% CI: 0.29–0.90; p < 0.00001). For the step length outcome, the intervention was most effective for a disease duration of 3–6 months (SMD = 0.27; 95% CI: 0.06–0.56; p = 0.04). No significant effects were observed for durations of 1–3 months (SMD = 0.44; 95% CI: −0.33 to 1.21; p = 0.26) or more than 6 months (SMD = 0.30; 95% CI: −0.03 to 0.64; p = 0.08). The best results were achieved with an intervention time of 4–8 weeks (SMD = 0.83; 95% CI: 0.54–1.12; p < 0.00001). Interventions lasting 1–4 weeks (SMD = 0.17; 95% CI: −0.15 to 0.48; p = 0.29) or more than 8 weeks (SMD = 0.30; 95% CI: −0.03 to 0.64; p = 0.08) showed no statistically significant effects. A maximum body weight support of 30% or more was most effective (SMD = 0.79; 95% CI: 0.47–1.11; p < 0.00001). Support of 0–30% (SMD = 0.14; 95% CI: −0.15 to 0.43; p = 0.35) was not statistically significant. A maximum gait speed of 0.2 m/s or more yielded the best results (SMD = 0.85; 95% CI: 0.38–1.31; p = 0.0003), while speeds of 0–0.2 m/s (SMD = 0.26; 95% CI: −0.02 to 0.54; p = 0.05) showed no significant effect. In summary, BWST with a disease duration of 3–6 months, an intervention time of 4–8 weeks, a maximum body weight support of 30% or more, and a maximum training gait speed of 0.2 m/s or more demonstrated the most effective improvement in balance and walking function in stroke patients.

Table 4
www.frontiersin.org

Table 4. Subgroup analysis of moderating variables affecting walking function.

Meta-regression analysis showed (as shown in Table 5) that the test results for heterogeneity of the disease duration, intervention time, maximum body weight support and maximum training gait speed were not statistically different.

Table 5
www.frontiersin.org

Table 5. Meta-regression analysis of the effects of different moderating variables on walking function.

Sensitivity analyses

Due to the high degree of heterogeneity between studies, a study-by-study culling approach was adopted to assess the impact of a single study on the overall effect size based on the overall study. The analysis revealed that the exclusion of single studies had minimal impact on the overall effect sizes for BBS scores (Figure 6) and gait speed (Figure 7A), indicating the robustness and reliability of the findings for these outcomes.

Figure 6
www.frontiersin.org

Figure 6. Sensitivity analysis of BWST on BBS scores.

Figure 7
www.frontiersin.org

Figure 7. Sensitivity analysis of the effect of BWST on walking function (A: gait speed, B: step length).

However, for step length (Figure 7B), the heterogeneity was significantly reduced (I2 = 42%) following the exclusion of the study by Hu (36). This suggests that Hu’s study may have been a significant source of heterogeneity in the step length outcome. Despite this reduction in heterogeneity, the overall effect size for step length remained consistent before and after the exclusion of Hu’s study (Post-exclusion: SMD = 0.38; 95% CI: 0.14 to 0.62; p = 0.002). This stability in the effect size confirms that the findings regarding step length are reliable and not unduly influenced by a single study.

Publication bias

The funnel plot and Egger’s method were utilized to assess publication bias. The results indicated that BBS scores and walking function outcomes were symmetrically distributed around the funnel plot (Figure 8). Additionally, the Egger’s test did not reveal statistically significant differences (p > 0.05) (Table 6), suggesting a low probability of publication bias in the study’s outcomes.

Figure 8
www.frontiersin.org

Figure 8. Meta-analysis publication bias funnel plot (A: BBS score, B: gait speed, C: step length).

Table 6
www.frontiersin.org

Table 6. Egger’s method test results.

Discussion

Balance and walking deficits resulting from lower limb motor dysfunction are critical factors influencing stroke patients’ ability to return to self-care and reintegrate into family and society (11). The meta-analysis conducted in this study demonstrated that BWST significantly enhances balance and walking function in stroke patients compared to conventional rehabilitation training, aligning with findings from previous research (12, 13).

Several previous studies have confirmed the validity of BBS scores, gait speed and step length as effective measures for evaluating balance and walking function in patients (12, 13). Additionally, the theoretical foundation of BWST in improving motor function is well-established (9, 10), drawing from central pattern generator theory, motor control dynamical system theory, and the theory of compulsory use (9). The mechanism of BWST involves mandatory exercise with reduced body weight and regulated gait speed, which enhances leg coordination in stroke patients (25) and improves motor relearning and neural pathway reorganization (9, 10).

During training, the therapist can integrate weight bearing, stepping, and balance components by adjusting training loads and body weight support according to the patient’s pathology, thereby enhancing proprioceptive input to the lumbar spinal cord and optimizing motor neural pathways, which promotes the consolidation of normal motor patterns (28). Moreover, from a psychological point of view, walking training with adequate safety measures provides patients with a sense of security, reducing anxiety and fear of falling (28). In summary, previous studies have addressed the mechanism of BWST to improve patients’ motor function in terms of movement pattern control and development, neural pathway conduction, and psychology. While the mechanisms underlying BWST’s effects on motor function are well-explored, there is limited research on the impact of individual differences, training intensity, and duration. Future studies should investigate these aspects further to provide a comprehensive understanding of BWST’s therapeutic effects.

The impact of BWST timing parameters on intervention outcomes can be examined through two key dimensions: the initiation and duration of the intervention. This study’s subgroup analysis revealed that the intervention time of 4–8 weeks was the best intervention program to improve stroke patients’ balance and walking function during 3–6 months of the patient’s disease duration. Hayes et al. (50) noted that early rehabilitation training can facilitate faster recovery of lower limb function in post-stroke patients, promoting brain cell regeneration around lesions and enhancing motor function compensation and reorganization in the contralateral cerebral hemisphere (51). However, the specific timing of BWST relative to routine rehabilitation is unclear. Song et al. (52) found that BWST is appropriate for patients with stable conditions and lower limb muscle strength of grade 3 or higher. Tong et al. (18) underscored the efficacy of early BWST intervention for recovering lower limb walking function in stroke patients, particularly within the first month of disease duration. Nevertheless, their study focused on patients with a disease duration of less than two months, limiting insights into longer durations. In addition, different intervention times also have a greater impact on the treatment effects of patients, but there are few comparisons of treatment effects based on different intervention cycles. This study demonstrates that for stroke patients with a disease duration of 3–6 months, an intervention period of 4–8 weeks yields the most favorable outcomes. Further research should explore these findings by including diverse patient populations and controlling intervention timing through randomized controlled trials.

The impact of training load parameters on intervention outcomes is evident in two primary areas: the degree of body weight support and the training gait speed. Previous studies have yielded varying results regarding the optimal degree of body weight support. Liu et al. (15) found that exceeding 50% of the maximum body weight support could induce gait abnormalities, hindering motor function recovery. Conversely, Hesse et al. (53) recommended that body weight support should not surpass 30%. However, the present study’s subgroup analysis demonstrated that a maximum body weight support exceeding 30% was more effective for rehabilitation, which diverges from earlier findings. This discrepancy may be attributed to differences in patient characteristics, as previous studies (15, 53) had small sample sizes and patients with a disease duration of approximately 40 days, potentially limiting their conclusions. Expanding patient characteristics and sample size in this study may account for the differing results, warranting further investigation.

Regarding setting the maximum training gait speed, Van et al. (54) argued against using lower speeds for gait training, as it might diminish muscle activation and cause abnormal gait patterns. Wu Hua et al. (16) found that a maximum gait training speed of 0.3 m/s yielded the most significant motor feedback improvement in stroke patients, whereas higher speeds (0.45 m/s) did not enhance motor function. The current study indicates that a maximum training gait speed of 0.2 m/s or more provides the most effective therapeutic outcomes for balance and walking function in stroke patients, suggesting that lower speeds are less effective, though the impact of higher speeds remains unclear. Proper adjustment of training loads according to patient mobility is crucial (55). For less mobile patients, increased body weight support or lower gait speeds may facilitate recovery, while more mobile patients might benefit less. This study’s subgroup analyses did not account for variations in patient mobility, and the limitations of included studies restricted further refinement of body weight support and gait speed classifications. Future research should explore the effects of varying body weight support ratios and gait speeds on recovery outcomes by integrating patient characteristics and training loads.

Despite the comprehensive analysis and assessment of all eligible studies, this review has several limitations. Firstly, many of the included studies were of low quality and had a certain risk of bias, which may affect the reliability of the study conclusions. Secondly, literature was excluded due to the absence of relevant outcomes, suggesting that the range of outcomes could be expanded in future research. Thirdly, some subgroups in the analyses were based on a limited number of studies, and the objectivity of these conclusions needs further validation. Future research should focus on randomized controlled trials with larger sample sizes to enhance the robustness of the findings. Additionally, further discussions should explore the impact of variations in patient characteristics and interventions to validate the conclusions of this study.

Conclusion

Compared to conventional rehabilitation, BWST demonstrated superior effectiveness in enhancing balance and walking function in stroke patients. The optimal intervention protocol identified was a 4–8 week treatment time, with a maximum body weight support of 30% or more, and a maximum training gait speed of 0.2 m/s or higher, applied during a 3–6 months disease duration.

Data availability statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.

Author contributions

ZJ: Conceptualization, Data curation, Formal analysis, Methodology, Writing – original draft. XZ: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Resources, Software, Writing – original draft. QF: Data curation, Methodology, Writing – original draft. YT: Conceptualization, Data curation, Supervision, Writing – review & editing.

Funding

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This study was supported by Innovation Project of Guangxi Graduate Education (XYCBZ2024014).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Mustafaoglu, R, Erhan, B, Yeldan, I, Huseyinsinoglu, BE, Gunduz, B, and Ozdincler, AR. The effects of body weight-supported treadmill training on static and dynamic balance in stroke patients: a pilot, single-blind, randomized trial. Turk J Phys Med Rehabil. (2018) 64:344–52. doi: 10.5606/tftrd.2018.2672

PubMed Abstract | Crossref Full Text | Google Scholar

2. Gelaw, AY, Janakiraman, B, Teshome, A, and Ravichandran, H. Effectiveness of treadmill assisted gait training in stroke survivors: a systematic review and meta-analysis. Global Epidemiol. (2019) 1:100012. doi: 10.1016/j.gloepi.2019.100012

Crossref Full Text | Google Scholar

3. Cabanas-Valdés, R, Boix-Sala, L, Grau-Pellicer, M, Guzmán-Bernal, JA, Caballero-Gómez, FM, and Urrútia, G. The effectiveness of additional Core stability exercises in improving dynamic sitting balance, gait and functional rehabilitation for subacute stroke patients (CORE-trial): study protocol for a randomized controlled trial. Int J Environ Res Public Health. (2021) 18:6615. doi: 10.3390/ijerph18126615

PubMed Abstract | Crossref Full Text | Google Scholar

4. Miyata, K, Hasegawa, S, Iwamoto, H, Otani, T, Kaizu, Y, Shinohara, T, et al. Structural validity of balance evaluation systems test assessed using factor and Rasch analyses in patients with stroke. J Phys Ther Sci. (2018) 30:1446–54. doi: 10.1589/jpts.30.1446

PubMed Abstract | Crossref Full Text | Google Scholar

5. Mehrholz, J, Pohl, M, Kugler, J, and Elsner, B. The improvement of walking ability following stroke. Deutsches Arzteblatt Int. (2018) 115:639–45. doi: 10.3238/arztebl.2018.0639

PubMed Abstract | Crossref Full Text | Google Scholar

6. Liu, Z, Gao, F, Zhu, T, Xu, B, Hao, Y, Zhao, YH, et al. Efficacy of weight lose training in anterior cruciate ligament reconstruction: a systematic review and meta-analysis. China Sport Sci. (2023) 43:78–97.

Google Scholar

7. Moseley, AM, Stark, A, Cameron, ID, and Pollock, A. Treadmill training and body weight support for walking after stroke. Cochrane Database Syst Rev. (2005) 4:Cd002840. doi: 10.1002/14651858.CD002840.pub2

Crossref Full Text | Google Scholar

8. Wang, J, Zhao, L, Gao, Y, Liu, C, Dong, X, and He, X. The difference between the effectiveness of body-weight-supported treadmill training combined with functional electrical stimulation and sole body-weight-supported treadmill training for improving gait parameters in stroke patients: a systematic review and meta-analysis. Front Neurol. (2022) 13:1003723. doi: 10.3389/fneur.2022.1003723

Crossref Full Text | Google Scholar

9. Trueblood, PR. Partial body weight treadmill training in persons with chronic stroke. Neuro Rehabilitation. (2001) 16:141–53. doi: 10.3233/NRE-2001-16303

PubMed Abstract | Crossref Full Text | Google Scholar

10. Harris-Love, ML, Forrester, LW, Macko, RF, Silver, KH, and Smith, GV. Hemiparetic gait parameters in overground versus treadmill walking. Neurorehabil Neural Repair. (2001) 15:105–12. doi: 10.1177/154596830101500204

Crossref Full Text | Google Scholar

11. Huang, J, Tan, XL, Guan, HY, and Lan, JN. A study of weight-supported plate walking training for improving lower limb function in stroke patients. Chinese Manipul Rehabil Med. (2022) 13:33–7.

Google Scholar

12. Srivastava, A, Taly, AB, Gupta, A, Kumar, S, and Murali, T. Bodyweight-supported treadmill training for retraining gait among chronic stroke survivors: a randomized controlled study. Ann Phys Rehabil Med. (2016) 59:235–41. doi: 10.1016/j.rehab.2016.01.014

Crossref Full Text | Google Scholar

13. Lura, DJ, Venglar, MC, van Duijn, AJ, and Csavina, KR. Body weight supported treadmill vs. overground gait training for acute stroke gait rehabilitation. Int J Rehabil Res. (2019) 42:270–4. doi: 10.1097/MRR.0000000000000357

PubMed Abstract | Crossref Full Text | Google Scholar

14. Srivastava, S, Seamon, BA, Patten, C, and Kautz, SA. Variation of body weight supported treadmill training parameters during a single session can modulate muscle activity patterns in post-stroke gait. Exp Brain Res. (2023) 241:615–27. doi: 10.1007/s00221-023-06551-7

PubMed Abstract | Crossref Full Text | Google Scholar

15. Liu, Z, Li, DX, and Sun, QL. Comparison of the effects of different weight-loss walking training modalities on the functional recovery of the lower limbs in stroke patients. Anhui Med J. (2023) 44:548–51.

Google Scholar

16. Wu, H, Gu, XD, Fu, JM, Yao, YH, Li, Y, Fu, XW, et al. Effects of different forms of weight-supported plate training on walking speed and lower limb joint motion in stroke patients. Zhejiang Med J. (2016) 38:1196–9.

Google Scholar

17. Jin, JP, Wu, XQ, You, Y, Zhang, LJ, and Chen, Y. Clinical research of the best start time of partial weight support for stroke patients with hemiplegia. Shanghai Med Pharmaceutical J. (2014) 35

Google Scholar

18. Dong, JP, Zhao, CY, Deng, XQ, Wang, LH, and Xiao, Q. Partial body weight support on walking ability for stroke following hemiplegia at early stage. Chin J Rehabil Theory Pract. (2010) 16:958–60.

Google Scholar

19. Wu, SL, Ma, C, Zeng, HH, and Mai, MQ. The effects of body weight support treadmill training on hemiplegic patients after stroke. Chin J Rehabil Med. (2007) 22:908–11.

Google Scholar

20. Moher, D, Liberati, A, Tetzlaff, J, and Altman, DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. J Clin Epidemiol. (2009) 62:1006–12. doi: 10.1016/j.jclinepi.2009.06.005

Crossref Full Text | Google Scholar

21. Higgins, JP, Altman, DG, Gøtzsche, PC, Jüni, P, Moher, D, Oxman, AD, et al. The Cochrane Collaboration's tool for assessing risk of bias in randomized trials. BMJ. (2011) 343:d5928. doi: 10.1136/bmj.d5928

PubMed Abstract | Crossref Full Text | Google Scholar

22. Cohen, J. Statistical power analysis for the behavioral sciences. Hillsdale: Erlbaum (1988).

Google Scholar

23. Zhang, X, Jing, F, Liu, Y, Tang, J, Hua, X, Zhu, J, et al. Effects of non-invasive brain stimulation on walking and balance ability in Parkinson's patients: a systematic review and meta-analysis. Front Aging Neurosci. (2022) 14:1065126. doi: 10.3389/fnagi.2022.1065126

Crossref Full Text | Google Scholar

24. Visintin, M, Barbeau, H, Korner-Bitensky, N, and Mayo, NE. A new approach to retrain gait in stroke patients through body weight support and treadmill stimulation. Stroke. (1998) 29:1122–8. doi: 10.1161/01.STR.29.6.1122

PubMed Abstract | Crossref Full Text | Google Scholar

25. Huang, XL, Wang, P, Wang, W, Cheng, Y, and Yu, L. The effect of supported treadmill ambulation training on hemiplegic patients after stroke. Chin J Phys Med Rehabil. (2003) 25:544–7.

Google Scholar

26. Yang, YQ, and Zhang, T. The effects of body weight support treadmill training on hemiplegic gait after stroke. Chin J Rehabil Med. (2004) 19:731–3.

Google Scholar

27. Yang, ZZ, Feng, WN, and He, XQ. Effects of weight-supported walking training on walking function in hemiplegic patients with stroke. Chin J Integrat Med Cardio-Cerebrovasc Dis. (2006) 4:720–1.

Google Scholar

28. Zheng, SC, Zhu, SW, Li, YZ, Song, CZ, Wu, J, and Ma, PX. The effect of early weight-supported plate walking training on hemiplegic patients with stroke. Chin J Rehabil Theory Pract. (2006) 11:463–4.

Google Scholar

29. Dias, D, Laíns, J, Pereira, A, Nunes, R, Caldas, J, Amaral, C, et al. Can we improve gait skills in chronic hemiplegics? A randomized control trial with gait trainer. Eura Medicophys. (2007) 43:499–504.

PubMed Abstract | Google Scholar

30. Chao, ZJ, Zhu, ZL, Xie, RZ, Feng, JJ, and Wang, WQ. Weight-loss walking training in the rehabilitation period of elderly stroke patients with hemiplegia. Shandong Med J. (2008) 48:43–4.

Google Scholar

31. Lin, JQ, Sun, XM, Gong, YF, and Ye, H. Effect of body-weight supported treadmill training on hemiplegic patients after stroke. Chin J Rehabil Theory Pract. (2008) 14:826–7.

Google Scholar

32. Lin, CY, Yang, B, and Qu, JP. Effects of partial body weight supported stand training on depression and balance function after massive cerebral infarction in early stage. Chin J Rehabil Theory Pract. (2008) 14:459–60.

Google Scholar

33. Huang, Y, Chen, RL, Wan, XL, and Pan, CH. Effects of partial body weight support treadmill training on motor function of lower limbs in patients with hemiparalysis after cerebral infarction. J Pract Med. (2009) 25:2270–2.

Google Scholar

34. Yan, Y, and Lai, YC. Effects of weight-supported walking training on lower limb motor function in stroke patients with hemiplegia. J Modern Med Health. (2009) 25:63–4.

Google Scholar

35. Su, XJ, and Bao, SY. The value of weight-supported walking training in the rehabilitation of lower limb motor and balance functions after stroke. Chinese J Pract Nerv Dis. (2011) 14:50–1.

Google Scholar

36. Hu, RL, Yu, JM, Li, GD, Chen, SL, Lai, LP, and Liu, T. The effect on the rehabilitation of hemiplegia with the body weight support treadmill training for ischemic stroke patients. China Prac Med. (2012) 7:27–9.

Google Scholar

37. Liu, XD, Dong, JG, and Sun, L. Efficiency of the body weight supported treadmill training (BWSTT) on lower limbs motor function in stroke hemiplegic patients. China J Modern Med. (2013) 23:85–8.

Google Scholar

38. Middleton, A, Merlo-Rains, A, Peters, DM, Greene, JV, Blanck, EL, Moran, R, et al. Body weight-supported treadmill training is no better than Overground training for individuals with chronic stroke: a randomized controlled trial. Top Stroke Rehabil. (2014) 21:462–76. doi: 10.1310/tsr2106-462

PubMed Abstract | Crossref Full Text | Google Scholar

39. Li, JT, Zhao, X, Huo, HY, Cao, L, and Yuan, ZL. The effect of weight-supported walking training on the recovery of lower limb mobility in stroke patients. Shandong Med J. (2014) 54:40–1.

Google Scholar

40. Tang, YQ, Xie, R, and Yang, WH. The efficacy of weight-supported walking training to improve walking ability in stroke patients. World Latest Med Informat. (2014) 11:84–5.

Google Scholar

41. Mao, Y, Lo, WL, Lin, Q, Li, L, Xiao, X, Raghavan, P, et al. The effect of body weight support treadmill training on gait recovery, proximal lower limb motor pattern, and balance in patients with subacute stroke. Bio Med Res Int. (2015) 2015:175719:1–10. doi: 10.1155/2015/175719

Crossref Full Text | Google Scholar

42. Zhao, QY, Lin, Q, Yang, T, Xia, P, and Li, XP. The effeet of body weight supported treadmill training and muscle tone on motor function of lower extremities of stroke survivors. Chin J Phys med Rehabil. (2018) 40:821–5.

Google Scholar

43. Guo, YL, Feng, CR, Xie, MH, and Liu, CR. Efficacy of weight-loss walking training in patients with cerebellar infarction-type ataxia. J Med Theory Pract. (2020) 33

Google Scholar

44. Liu, S. Application of weight-loss walking training in stroke patients and improvement of walking function. Med Inf. (2020) 33:128–9.

Google Scholar

45. Liu, Z, and Liang, TJ. Effect of Mirror therapy combined with body weight supported treadmill training on walking function in Poststroke hemiplegia patients. Chinese Gen Pract. (2021) 24:2680–5.

Google Scholar

46. Lu, MS, and Gao, HL. Observation on the application effect of weight-loss walking training in patients with early hemiplegia after stroke. Clin Med Eng. (2021) 28:1371–2.

Google Scholar

47. Ma, L, and Liu, Y. Suspension weight support training in the rehabilitation of hemiplegic patients after stroke. J Med Forum. (2021) 42:120–2.

Google Scholar

48. Duran, UD, Duran, M, Tekin, E, Demir, Y, Aydemir, K, Aras, B, et al. Comparison of the effectiveness of anti-gravity treadmill exercises and underwater walking exercises on cardiorespiratory fitness, functional capacity and balance in stroke patients. Acta Neurol Belg. (2023) 123:423–32. doi: 10.1007/s13760-022-02012-0

PubMed Abstract | Crossref Full Text | Google Scholar

49. Wang, SX, Liu, XH, and Song, XJ. The effect of weight-supported plate walking training in the rehabilitation of hemiplegic patients with stroke. Chin Gen Pract Nurs. (2023) 21:91–4.

Google Scholar

50. Hayes, SH, and Carroll, SR. Early intervention care in the acute stroke patient. Arch Phys Med Rehabil. (1986) 67:319–21.

PubMed Abstract | Google Scholar

51. Miu, HS. Theory of functional recovery after central nerve injury. Chin J Rehabil. (1998) 13:97–9.

Google Scholar

52. Song, CZ, Cui, AQ, Li, YZ, Yue, SW, Sun, YB, and Zhu, SW. The role of ultra-early rehabilitation training on the recovery of psychosomatic function in patients with acute cerebral infarction. Chin J Tissue Eng Res. (2003) 7:1165.

Google Scholar

53. Hesse, S, Helm, B, Krajnik, J, Gregoric, M, and Mauritz, KH. Treadmill training with partial body weight support: influence of body weight release on the gait of Hemiparetic patients. Neurorehabil Neural Repair. (1997) 11:15–20. doi: 10.1177/154596839701100103

Crossref Full Text | Google Scholar

54. Van, KK, Boonstra, A, Reinders-Messelink, H, and den Otter, R. The combined effects of body weight support and gait speed on gait related muscle activity: a comparison between walking in the Lokomat exoskeleton and regular treadmill walking. PLoS One. (2014) 9:e107323. doi: 10.1371/journal.pone.0107323

Crossref Full Text | Google Scholar

55. Crompton, S, Khemlani, M, Batty, J, Ada, L, Dean, C, and Katrak, P. Practical issues in retraining walking in severely disabled patients using treadmill and harness support systems. Australian J Physiother. (2001) 47:211–3. doi: 10.1016/S0004-9514(14)60268-3

Crossref Full Text | Google Scholar

Keywords: body weight support training, stroke, balance, walking function, meta-analysis

Citation: Jiang Z, Zhang X, Fu Q and Tao Y (2024) Effects of body weight support training on balance and walking function in stroke patients: a systematic review and meta-analysis. Front. Neurol. 15:1413577. doi: 10.3389/fneur.2024.1413577

Received: 29 April 2024; Accepted: 15 August 2024;
Published: 27 August 2024.

Edited by:

Masahiro Sakita, Kyoto Tachibana University, Japan

Reviewed by:

Marco Battaglia, University of Eastern Piedmont, Italy
Wang Hui, Chinese Academy of Sciences (CAS), China

Copyright © 2024 Jiang, Zhang, Fu and Tao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Yimin Tao, dHltQGd1YXQuZWR1LmNu

These authors have contributed equally to this work and share first authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.