Skip to main content
Wiley Open Access Collection logoLink to Wiley Open Access Collection
. 2025 May 9;31(3):e70020. doi: 10.1111/ijn.70020

Effectiveness of Treadmill Training Intervention for the Management of Patients With Stroke: A Systematic Review and Meta‐Analysis

Chenyi Shi 1, Yuxi Xiao 2,, Dawei Zang 1, Hongjun Ren 2
PMCID: PMC12063472  PMID: 40344634

ABSTRACT

Background

Treadmill training, including body weight–supported treadmill training (BWSTT), is widely used in stroke rehabilitation. However, its efficacy in improving walking outcomes may vary depending on patients' baseline functional status.

Objective

This study aims to systematically evaluate effectiveness of treadmill training on walking speed and endurance in stroke survivors and to assess influence of baseline dependency and use of BWSTT.

Methods

We performed systematic review and meta‐analysis as per PRISMA 2020 guidelines. Comprehensive search was conducted using Scopus, MEDLINE, EMBASE, Chinese Biomedical Literature Database, China National Knowledge Infrastructure, Cochrane Library, Google Scholar and ScienceDirect for studies published from January 1964 to April 2024. Eligible studies were randomized controlled trials assessing treadmill training in stroke patients with outcomes as walking speed and/or endurance. Data extraction and risk of bias assessment were independently performed by two reviewers using Cochrane Risk of Bias‐2 tool. Standardized mean differences (SMDs) and 95% confidence intervals (CIs) were calculated using random effects model. Subgroup analyses were conducted based on baseline dependency and BWSTT use.

Results

Fifty‐nine studies were included. Meta‐analysis demonstrated significant improvements in walking speed (SMD = 0.255; 95%CI: 0.141–0.369) and walking endurance (SMD = 0.277; 95%CI: 0.134–0.421) among stroke survivors receiving treadmill training. Subgroup analysis revealed that independent participants experienced greater benefits in walking speed (SMD = 0.345) and endurance (SMD = 0.374) compared to dependent participants. Studies employing BWSTT reported enhanced outcomes relative to those without BWSTT. Moderate to high heterogeneity was observed, and publication bias was detected.

Conclusion

Treadmill training, particularly when combined with BWSTT, effectively enhances walking speed and endurance in stroke survivors.

Keywords: cerebral infarction, meta‐analysis, stroke, treadmill training


Summary.

  • What Is Already Known About This Topic?

  • Treadmill training, including body weight‐supported treadmill training (BWSTT), is a potential rehabilitation intervention for stroke survivors to improve walking speed and endurance.

  • Previous studies have shown mixed results regarding the effectiveness of treadmill training compared to other rehabilitation methods.

  • Key knowledge gaps include the differential impact of treadmill training based on patients' initial functional status and the specific benefits of incorporating BWSTT.

  • What This Paper Adds?

  • This meta‐analysis demonstrates significant improvements in walking speed (SMD = 0.255) and walking endurance (SMD = 0.277) in stroke survivors following treadmill training.

  • Subgroup analyses reveal that independent participants benefit more significantly in both walking speed and endurance compared to dependent participants.

  • Studies employing BWSTT show greater improvements in walking outcomes, highlighting the added value of this technique in stroke rehabilitation.

  • The Implications of This Paper

  • How do these findings influence policy?

  • These findings suggest that treadmill training, especially with BWSTT, should be considered for inclusion in standard stroke rehabilitation programs due to its effectiveness in improving mobility.

  • How can these findings be used in practice?

  • Clinicians can better tailor rehabilitation programs by incorporating treadmill training, particularly for patients who are initially independent, to maximize improvements in walking speed and endurance.

  • How do these findings impact research and education?

  • Future research should focus on standardizing treadmill training protocols, comparing different types of treadmill interventions and exploring long‐term outcomes. Educational programs should emphasize the benefits of treadmill training in stroke rehabilitation.

1. Introduction

Stroke represents a significant global health challenge, affecting millions of individuals annually and leading to a wide range of disabilities (Khaku and Tadi 2024). These disabilities can vary widely from mild impairments to severe physical and cognitive dysfunction, depending on the stroke's severity and the brain area affected (Elendu et al. 2023). Despite advances in acute stroke management, the long‐term rehabilitation of stroke survivors remains a critical area for healthcare providers and researchers, with the primary goal of enhancing functional recovery and improving quality of life (Boehme et al. 2021). Moreover, as walking is pivotal to autonomy and overall well‐being, regaining independent ambulation is widely recognized as the primary goal in stroke rehabilitation.

Treadmill training, as a form of physical therapy, has gained prominence in poststroke rehabilitation programs (Damiano and DeJong 2009). This intervention leverages the natural pattern of walking, which is often severely affected following a stroke. The rationale behind treadmill training is based on the concept of neuroplasticity—the brain's ability to reorganize itself by forming new neural connections (Harvey 2009; Xiao et al. 2012). This ability allows for the compensation of damaged areas and the restoration of lost functions to some extent. Additionally, treadmill training is believed to stimulate central pattern generators (CPGs) in the spinal cord—intrinsic neural circuits that generate rhythmic and coordinated movements—thereby supporting the recovery of automatic, independent walking patterns in stroke survivors (Sun et al. 2013).

One of the key advantages of treadmill training includes its ability to provide a controlled environment where the intensity, speed and duration of exercise can be systematically adjusted to meet the specific needs of each patient (McCain et al. 2008). This customization is crucial since stroke survivors often exhibit varied levels of motor function impairments. Moreover, modern treadmills equipped with body weight support systems can further assist those who are initially unable to support their weight or maintain balance, thereby facilitating an earlier start to walking exercises than might otherwise be possible (Yamamoto et al. 2022).

The effectiveness of treadmill training in the rehabilitation of patients with stroke has been supported by various studies highlighting improvements in gait speed, endurance and overall walking ability (Deniz et al. 2011; DePaul et al. 2015; Kelley et al. 2013; Kaźmierczak et al. 2022). These enhancements are critical, as they contribute directly to the independence and quality of life of stroke survivors. However, the degree to which treadmill training is beneficial when compared to other rehabilitation interventions remains a subject of considerable debate within the medical community.

Furthermore, the timing of intervention initiation poststroke is a pivotal factor that potentially influences the outcomes of treadmill training (Deniz et al. 2011; DePaul et al. 2015; Kaźmierczak et al. 2022; Kelley et al. 2013). Early intervention may capitalize on the heightened state of neuroplasticity immediately following a stroke, possibly leading to more significant improvements in motor skills (Laufer et al. 2001; McCain et al. 2008). Conversely, late initiation of treadmill training, while still beneficial, might not offer the same level of impact due to the reduced plasticity of the brain as time progresses (Aguiar et al. 2020; Baek et al. 2021; Brauer et al. 2022; Hornby et al. 2019; Kim and Yim 2017; Nave et al. 2019; Serra et al. 2022; Cakmak et al. 2024).

Adding to the complexity, individual characteristics of patients with stroke—such as severity of stroke, specific brain regions affected and the presence of other comorbid conditions—can significantly modify the effectiveness of any rehabilitation technique, including treadmill training. Therefore, personalized approaches to rehabilitation, which consider these individual differences, are increasingly advocated in clinical settings.

In this context, comprehensive review of available literature on treadmill training for patients with stroke can provide valuable insights. By aggregating and analysing data from multiple studies, this approach offers a robust assessment of the effectiveness of treadmill training interventions, helping to clarify their benefits and limitations. Such an analysis is crucial not only for clinicians seeking to optimize rehabilitation strategies but also for stakeholders involved in health policy and resource allocation in stroke care. Hence, this review was done to determine the effectiveness of treadmill training intervention for managing patients with stroke.

2. Materials and Methods

2.1. Eligibility Criteria

The inclusion criteria are defined as follows:

Study Design: Only individual or cluster randomized controlled trials (RCTs) with a parallel arm or cross‐over structure were included.

Publication Criteria: The review has considered only published full‐text articles. Case reports, series, conference abstracts and unpublished grey literature will be excluded.

Population: Studies targeting patients diagnosed with stroke (ischaemic or haemorrhagic), without limitations based on age, gender or the presence of comorbidities.

Interventions: Studies that evaluate the effectiveness of treadmill training interventions for stroke rehabilitation. Comparisons may include standard care practices or other rehabilitative interventions.

Outcomes: Studies must report on any of the following outcomes: walking speed and walking endurance.

2.2. Search Strategy

A comprehensive and meticulous literature search was conducted across multiple databases, including Scopus, MEDLINE, EMBASE, Chinese biomedical literature database, China National Knowledge Infrastructure, Cochrane Library and search engines like Google Scholar and ScienceDirect. We employed both medical subject headings (MeSH) and free‐text terms, using Boolean operators to refine the search. The key terms were related to stroke, treadmill training and randomized controlled trials. The search was limited to articles published from January 1964 to April 2024 and was conducted in both English and Chinese languages. Additionally, we examined the references of the retrieved studies to identify any potentially overlooked articles. The search strategy for this review is outlined in the Supporting Information Appendix.

2.3. Study Screening

During the initial phase of study selection, titles, keywords and abstracts were independently screened by two reviewers. Subsequently, they accessed and assessed the full texts of potentially relevant studies based on the pre‐established eligibility criteria. Any discrepancies during the initial screening phase were settled through discussion and consensus between the two reviewers. In the second phase, thorough examination of full texts was performed, finalizing those studies that fulfilled the inclusion criteria.

2.4. Data Extraction

After identifying the studies suitable for inclusion, the two reviewers engaged in data collection using a specially designed semistructured data extraction form, which was developed during the planning phase of the review. This form facilitated the systematic collection of critical information such as the authors' names, title of the study, publication year, study duration, research design, location and setting of the study, number of participants, tools used for outcome assessment, average age of participants and detailed descriptions of the interventions and control conditions. Data entry was conducted by the first reviewer and subsequently checked for precision by the second reviewer.

2.5. Risk of Bias Assessment

The primary and secondary researchers undertook the responsibility of evaluating the risk of bias in the studies that were included. They employed the Cochrane Risk of Bias tool for Randomized Controlled Trials (RoB 2) to scrutinize five distinct areas: bias stemming from the randomization process, deviations from the planned intervention, incomplete outcome data, the accuracy of outcome measurement and bias in the reporting of results (Sterne et al. 2019). Following these evaluations, each study was classified as exhibiting low, high or moderate concerns related to bias, which in turn helped to ascertain the quality of the evidence provided.

2.6. Statistical Analysis

Meta‐analysis was performed using STATA software, version 17. Since both the outcomes were continuous, standardized mean difference (SMD) was computed along with 95% confidence intervals (Cis), using means, standard deviations and sample sizes from each group. Random effects model was utilized, applying the inverse variance method for the weighting of studies. Forest plots were created to illustrate both individual study results and combined estimates (Cumpston et al. 2019).

Heterogeneity among the studies was evaluated using chi‐square test and I 2 statistics. Subgroup analyses were carried out focusing on variables such as the independence of participants at the time of recruitment and the use of body weight‐supported treadmill training (BWSTT) techniques. For the purposes of this review, ‘dependent group’ is defined as stroke survivors who, at baseline, required physical assistance or relied on assistive devices for ambulation, as determined by standardized functional assessments (e.g., the Functional Ambulation Categories). Importantly, the use of BWSTT is considered an intervention modality and does not, in itself, classify a patient as dependent; rather, dependency is solely based on baseline ambulation ability. Publication bias was examined using Egger's test and visualized through funnel plots. An asymmetrical funnel plot or an Egger's test p‐value less than 0.05 was indicative of potential publication bias (Cumpston et al. 2019).

3. Results

3.1. PRISMA Flow Diagram

Review process commenced with identification of 3193 records through various databases. After removing 432 duplicates, 2761 records were screened, leading to 238 full‐text articles being assessed for eligibility (Figure 1). Ultimately, 59 studies met the inclusion criteria and were incorporated into the review (Ada et al. 2003, 2013; Aguiar et al. 2020; Baek et al. 2021; Bonnyaud et al. 2013a, 2013b; Brauer et al. 2022; Combs‐Miller et al. 2014; Da Cunha Filho et al. 2002; Deniz et al. 2011; DePaul et al. 2015; Duncan et al. 2011; Eich et al. 2004; Franceschini et al. 2009; Gama et al. 2017; Globas et al. 2011; Hornby et al. 2008, 2019; Hoyer et al. 2012; Jaffe et al. 2004; Kang et al. 2012; Kaźmierczak et al. 2022; Kelley et al. 2013; Kim et al. 2011, 2016; Kim and Yim 2017; Kosak and Reding 2000; Kuys et al. 2011; Langhammer and Stanghelle 2010; Laufer et al. 2001; Liston et al. 2000; Luft et al. 2008; Mackay‐Lyons et al. 2013; Macko et al. 2005; Mao et al. 2015; Middleton et al. 2014; Moore et al. 2010; Nave et al. 2019; Nilsson et al. 2001; Olawale et al. 2009; Park et al. 2013, 2015; Pohl et al. 2002; Ribeiro et al. 2013; Richards et al. 1993, 2004; Serra et al. 2022; Srivastava et al. 2016; Sullivan et al. 2007; Suputtitada et al. 2004; Takami and Wakayama 2010; Cakmak et al. 2024; Toledano‐Zarhi et al. 2011; Weng et al. 2004, 2006; Werner et al. 2002; Yen et al. 2008; Zhu et al. 2004).

FIGURE 1.

FIGURE 1

PRISMA flowchart.

3.2. Included Study Characteristics

Characteristics of the included studies are provided in Table 1.

TABLE 1.

Characteristics of the included studies (N = 59).

Author and year of publication Study country Study design Participant details Intervention details Control details Duration of follow‐up Sample size (I) Sample size (C) Mean age (in years) (I) Mean age (in years) (C) Risk of bias
Ada et al. (2003) Australia Parallel arm RCT Patients within 28 days of their first stroke, between 50 and 85 years of age. Involved walking on a treadmill supported in a harness Assisted overground walking 6 months 64 62 NR NR Low
Ada et al. (2013) Australia Three‐arm parallel RCT People with chronic stroke ambulatory at study onset

Group A undertook 30 min of treadmill and overground walking three times per week for 4 months

Group B undertook treadmill training for 2 months

No intervention 12 months 34 34

A‐63

B‐64

70 Low
Aguiar et al. (2020) NR Parallel arm RCT People with chronic stroke Treadmill Training (40 min, three times/w, 12 weeks Total 1440 min) Physiotherapy Interventions (40 min, three times/w, 12 w, total 1440 min) 4 months 11 11 52 48 Low
Baek et al. (2021) South Korea Single‐blind, two‐arm parallel RCT People with chronic stroke Each intervention comprised allocated treadmill training for 30 min and simple exercise for 30 min in the supine and sitting positions. Simple exercise included only passive stretching in the upper extremity, hip, and knee areas. Standard care 6 weeks 17 17 56.94 56.13 Low
Bonnyaud et al. (2013a) France Four arm Parallel RCT People with chronic stroke

GO: overground without a mass once for 20 min at comfortable speed

GOM: overground with a mass once for 20 min at comfortable speed

GT: treadmill without a mass once for 20 min at comfortable speed GTM: treadmill with a mass once for 20 min at comfortable speed

Standard care 20 min 60 NR 50 50 High
Bonnyaud et al. (2013b) France Parallel arm RCT People with chronic stroke and aged greater than 18 years, hemiparesis caused by a single hemispheric stroke, ability to walk 20 min without a break and without an assistive device GO: single overground gait‐training for 20 min in a corridor at comfortable speed Gait‐training for 20 min at comfortable speed 20 min 26 NR 50 50 High
Brauer et al. (2022) NR Parallel arm RCT People with Subacute stroke

Treadmill Training

9 TT: 30 min, three times/w, 8 weeks Conv GT: 30 min, two times/w, 8 weeks Total 1200 min)

Physiotherapy Interventions (30 min, five times/w, 8 w, total 1200 min) 26 weeks 60 59 62 64 Low
Cakmak et al. (2024) Turkey Parallel arm RCT People with chronic stroke Treadmill training for 3 consecutive weeks, 5 days a week, for 30 min each day and additional 30 min of BWSTT per session Control for 3 consecutive weeks, 5 days a week, for 30 min each day 3 weeks 14 16 55 57 High
Combs‐Miller et al. (2014) USA Parallel arm RCT Minimum of six months postischaemic or haemorrhagic stroke; age between 21 and 80 years BWSTT group undertook 30 min of treadmill training with systematically less body weight support (start at 30%), five times per week for 2 weeks OWT group B undertook overground walking training at fast speed, five times per week for 2 week 2 weeks 10 10 56 66 Low
Da Cunha Filho et al. (2002) NR Parallel arm RCT People with chronic stroke BWSTT: participants walked on a treadmill with up to 30% of their body weight supported using a harness Regular gait‐training (CTL): strengthening, functional and mobility activities 3 weeks 7 8 NR NR Low
DePaul et al. (2015) Canada Parallel arm RCT People with chronic stroke ambulatory at study onset MLWP group undertook a Motor Learning Walking Program and practiced various overground walking tasks for 40 min, 15 sessions over 5 weeks BWSTT group undertook a Body weight‐supported treadmill Training for 30 min, 15 sessions over 5 weeks 5 weeks 35 35 66 69 Low
Deniz et al. (2011) Turkey Parallel arm RCT People with chronic stroke ambulatory at study onset BWSTT, five times per week for 4 weeks (300 min a week) General physiotherapy, five times per week for 4 weeks (300 min a week) 1 month 10 10 62 62 Low
Duncan et al. (2011) USA Parallel arm RCT People age of 18 years or older, a stroke within 45 days before study entry Group 1 received training on a treadmill with the use of BWS 2 months after the stroke had occurred (early locomotor training) Group 2 received this training 6 months after the stroke had occurred (late locomotor training) Controls participated in an exercise program at home managed by a physical therapist 2 months after the stroke (home exercise program) 12 months 408 NR NR NR Low
Eich et al. (2004) NR Parallel arm RCT Patients first time supratentorial stroke; less than 6 weeks post‐stroke; aged 50–75 years Participants walked on a treadmill with up to 15% of their body weight supported using a harness; the slope and speed of the treadmill were adjusted to achieve a training heart rate Regular gait‐training: tone‐inhibiting and gait preparatory manoeuvres and walking practice on floor and stairs based on Bobath 3 months 25 25 NR NR Low
Franceschini et al. (2009) Italy Parallel arm RCT People with chronic stroke not ambulatory at study onset Conventional rehabilitative treatment plus gait‐training with BWSTT Conventional treatment with overground gait‐training only 1 month 52 50 66 71 Low
Gama et al. (2017) Brazil Parallel arm RCT Chronic hemiparetic gait after an ischaemic or hemorrhagic stroke, > 6 months from the stroke event Walking on a treadmill supported in a harness with BWSTT Assisted overground walking with BWS 1 and half months 16 16 NR NR Some concerns
Globas et al. (2011) Switzerland and Germany Parallel arm RCT Hemiparetic gait as evaluated by a neurologist with at least 1 clinical sign for paresis, spasticity or circumduction of the affected leg while walking and ambulatory at study onset 3 months (three times per week) progressive graded, high‐intensity aerobic treadmill exercise Conventional care physiotherapy 3 months 20 18 69 69 Some concerns
Hornby et al. (2008) USA Parallel arm RCT People with chronic stroke Locomotor training (LT) using a treadmill Conventional rehabilitation 6 months 24 24 57 57 Low
Hornby et al. (2019) NR Parallel arm RCT People with chronic stroke, able to walk ind ± aids at comf gait speed < 1.0 m/s over 10 m First group: 33 min, mean 3.375 times/w, 8 weeks Total 891 min Second group: 34 min, mean 3.375 times/w, 8 weeks Total 918 min

Stepping activities in variable contexts (37 min per session, three to five times/w, for 8 weeks Total 999 min)

3 months 30 32 60 56 Some concerns
Hoyer et al. (2012) Norway Parallel arm RCT People with chronic stroke Treadmill therapy Traditional gait‐training 3 months 30 30 52 52 Low
Jaffe et al. (2004) NR Parallel arm RCT Post‐stroke patients. Hemiplegia secondary to documented lesion; able to walk independently or with stand‐by supervision Treated as outpatients for 6 x 1‐h sessions per week for 2 weeks Stepping over real objects while walking overground 2 weeks 11 12 NR NR Some concerns
Kang et al. (2012) South Korea Parallel arm RCT People with chronic stroke 3 arms: 1. Wore a head‐mounted display to receive speed modulated optic flow during treadmill training for 30 min 2. Treadmill training 3. Regular therapy for the same time, three times per week for 4 weeks 1 month 11 111 10 56 56 Low
Kaźmierczak et al. (2022) Poland Parallel arm RCT People with chronic stroke aged 63 ± 12 years, with post‐ischemic subacute (within six months onset) stroke hemiparesis

Specific rehabilitation program plus additional treadmill training

Specific rehabilitation program 1 month 62 30 63 63 Low
Kelley et al. (2013) USA Parallel arm RCT People with chronic stroke Robotic‐assisted body weight supported treadmill training using the Lokomat® Ground gait training 2 months 11 9 67 64 High
Kim et al. (2011) South Korea

Parallel arm RCT

Stroke, able to maintain standing independently for 30 s and to walk independently more than 30 m and able to understand and follow instructions Treadmill training Lower extremity muscle strength training 1 and half month 20 24 NR NR

Some concerns

Kim et al. (2016) South Korea

Parallel arm RCT

Hemiplegia participants over six months after stroke, gait speed of less than 0.8 m/s,

VRCA group undertook a virtual reality treadmill training‐based community ambulation for 30 min, 12 sessions, 3 sessions per week

CA group undertook a community ambulation training, 30 min per session, three times per week for 4 weeks

General exercise program, 10 x 30‐min sessions per week for 4 weeks

1 month 10 in VRCA, 10 in CA group 10

VRCA‐63

CA‐64

70 Low
Kim and Yim 2017 South Korea Parallel arm RCT People with chronic stroke, able to independently walk Treadmill training + handgrip strengthening + conventional rehabilitation

Conventional rehabilitation

8 months 14 15 51 52 Low
Kosak and Reding 2000 NR Parallel arm RCT People with chronic stroke Participants walked on a treadmill and were provided with manual guidance for weight shifting, leg advancement, and foot placement Participants walked with the assistance of knee–ankle combination bracing and a hemibar (nontask‐oriented ‐ ‘orthopaedic’)

3 months

22 34 NR NR Low
Kuys et al. (2011) Australia Parallel arm RCT Diagnosis of first stroke confirmed by CT scan and scored 2 or more on the walking item of Motor Assessment Scale Walked on the treadmill for 30 min (excluding rests), three times a week for 6 weeks, at an intensity of 40% to 60% heart rate reserve or a Borg Rating of Perceived Exertion of 11 to 14

Usual physiotherapy intervention only

4 and half months 15 15 72 63 Low
Langhammer and Stanghelle 2010 Norway Parallel arm RCT People with chronic stroke Treadmill training (with handrails to hold on but no body weight or other safety support) Walking outdoors 17 days 21 18 75 74 Low
Laufer et al. (2001) NR Parallel arm RCT Participants with onset of stroke no more than 90 days prior to recruitment and ability to walk on treadmill. Participants walked on a treadmill at a comfortable speed with a therapist assisting leg movements and were permitted to use a handrail for external support if required; Participants walked on a floor surface using gait aids, assistance, and rest periods as needed 3 weeks 15 14 NR NR High
Liston et al. (2000) NR Cross‐over RCT People with higher level gait disorder and discharged from all rehabilitation services. Participants walked on a treadmill for as long as they felt comfortable, rest breaks were allowed and no body weight support was provided using a harness Schedule of 31 interventions in 3 treatment modules: gait ignition or failure, postural alignment and other 1 and half months 10 8

NR

NR

Low
Luft et al. (2008) USA Parallel arm RCT People older than 45 years of age with first clinical ischaemic stroke and chronic hemiparetic gait 6 or more months after completion of conventional subacute rehabilitation Treadmill training sessions. Duration and intensity started low and increased approximately by 5 min and 5% heart rate reserve every 2 weeks Standard Care 6 months 57 56 64 63 Low
Mackay‐Lyons et al. (2013) Canada Parallel arm RCT People older than 18 years, within 1 month of a first ischaemic stroke able to walk 5 m with or without assistance All individuals participated in 60‐min physiotherapy sessions five times weekly as inpatients for 6 weeks and three times weekly as outpatients for another 6 weeks for a total of 48 sessions. Standard Care 6 and 12 months 24 26 62 59 Low
Macko et al. (2005) NR Parallel arm RCT People with Chronic ischaemic stroke (less than 6 months) Participants walked on a treadmill to achieve a target aerobic intensity of 60% to 70% heart rate reserve (progressive aerobic training); no body weight support was provided using a harness Participants completed a supervised stretching and low‐intensity walking program 6 months 32 29 NR

NR

Low
Mao et al. (2015) China Parallel arm RCT People with first stroke, unilateral hemiparesis for no more than 3 months resulting and abnormal 10 m walk time Received body weight‐supported treadmill training 20 to 40 min five times per week for 3 weeks Underwent conventional overground walking for same amount of time NR 15 14 60

NR

Some concerns
Middleton et al. (2014) USA Parallel arm RCT People with age ≥ 18 years and presence of unilateral hemiplegia Undertook gait‐training on a treadmill with comfortable speed for 60 min and 120 min training for balance, strength, coordination and range of motion for 10 consecutive weekdays Received an overground gait‐training including training for balance, strength, coordination and range of motion, 3 h for 10 consecutive weekdays (total of 30 h) 3 and half months 27 23 61 61 High
Moore et al. (2010) USA Cross‐over RCT People who are ≤ 3 months after stroke, ability to stand or walk 5 m 20/30 participants with chronic stroke completed a repeated baseline measure with clinical physiotherapy; afterwards participants were randomized in a cross‐over trial and received 4 weeks of intensive locomotor training (A) or 4 weeks of no intervention (B) before cross over Standard Care NR 15 15 67 57

Some concerns

Nave et al. (2019) Germany Parallel arm RCT People who are aged more than 18 years, were in the subacute phase of ischaemic or haemorrhagic stroke Participants received either aerobic, bodyweight supported, treadmill based physical fitness training or relaxation sessions, each for 25 min, five times weekly for 4 weeks Relaxation sessions, that is, participants were instructed to contract the muscles for five to 10 s 6 months 105 95 69 70

Some concerns

Nilsson et al. (2001) (a) NR Parallel arm RCT First stroke with residual hemiparesis and aged less than 70 years Participants walked on a treadmill with up to two therapists assisting leg movements, they were permitted to use a handrail for external support, if required Participants practiced walking on a floor surface based on Motor Relearning Program guidelines 10 months 26 28

NR

NR

Low
Nilsson et al. (2001) (b) NR Parallel arm RCT First stroke with residual hemiparesis and aged less than 70 years Participants walked on a treadmill with up to 2 therapists assisting leg movements, they were permitted to use a handrail for external support, if required Participants practiced walking on a floor surface based on Motor Relearning Program guidelines 10 months 10 9

NR

NR

Low
Olawale et al. (2009) Nigeria Three‐arm parallel RCT People who had stroke > 3 months but < 24 months and can walk independently Treadmill training for, three times a week for 12 weeks (3 h a week) Control group 1 used standard physiotherapy, three times a week for 12 weeks (3 h a week) 2. CTL Control group 2 used standard physiotherapy including overground walking exercises for the same time and frequency 3 months 20 40 57 57 Some concerns
Park et al. (2013) South Korea Two arm parallel RCT Participants with onset of stroke 6 months or more prior to the study and can walk for 10 m or more without any aid

1. OGT group undertook overground gait‐training for 30 mins twice a day for 5 days

2. TGT group received treadmill gait‐training with increased speed for same amount of time

Not reported NR 20 20 53 53 Some Concerns

Park et al. (2015)

South Korea RCT People > 6 months and < 2 years after the onset of stroke can walk for 10 min or longer on a treadmill and also absence of neurotic diseases. Group undertook treadmill walking training with rhythmic auditory stimulation 30 min, five times per week for 3 weeks Group received overground walking training with rhythmic auditory stimulation for the same amount of time NR 9 10 53 53 High

Pohl et al. (2002)

NR Parallel arm RCT People with hemiparesis are caused by ischaemic stroke and are able to walk without assistance. Participants walked on a treadmill without therapist assistance, speed was progressed using an aggressive protocol Limited progressive treadmill training with body weight support. Conventional gait therapy NR 44 25 NR NR Some concerns
Ribeiro et al. (2013) Brazil Parallel arm RCT People of age 40 to 70 years with chronic stroke

Group underwent treadmill gait‐training base—30 min three times per week for 4 weeks

Training with comfortable speed for same amount of time NR 12 13 57 57 High

Richards et al. (1993)

NR Parallel arm RCT People aged 40 to 80 years and less than 7 days after onset of first stroke. Treatment started as early as possible after the stroke and included treadmill training, tilt table exercises and resisted exercises using isokinetic equipment.

Control group 1: Traditional physiotherapy based on neurophysiological techniques.

Control group 2: Less intense traditional physiotherapy based on neurophysiological techniques

3 to 6 months 10 17 NR NR Some concerns

Richards et al. (2004)

Canada RCT People aged between 30 and 89 years, with the first or second episode of ischaemic stroke with residual deficit. Received treadmill training without body weight support, reciprocal stepping and limb loading for the same time and frequency Received physiotherapy in an eclectic approach, five times per week for 8 weeks (5 h per week) 3 months 32 31 63 Years 61 Years Low

Serra et al. (2022)

USA Parallel arm RCT

People with > 50 years chronic (> 6 months) stroke survivors with hemiparetic gait

Were recruited

Participants completed three times /week aerobic treadmill rehabilitation Six months of two times/week stretching/balance 6 months 19 20 68 63 Some concerns
Srivastava et al. (2016) India

Three‐arm parallel RCT

People aged 16 to 65 years with duration of hemiparesis > 3 months and impaired ability to walk independently or with support

One group received gait‐training on a treadmill without bodyweight support.

Another group received gait‐training on a treadmill with partial body weight support (40% unweighting of body weight) all groups trained 30 mins per day, 5 day per week for 4 weeks

Overground task‐oriented gait‐training. 3 months 45 15 46 46 Low

Sullivan 2007

USA Four arm parallel RCT People aged 18 and above, ischaemic or haemorrhagic stroke

Group 1 received combined body weight‐supported treadmill training and upper extremity ergometry for the same time and frequency.

Group 2 received combined body weight‐supported treadmill training and resistive leg cycling for the same time and frequency.

Group 3 received combined body weight‐supported treadmill training and lower extremity progressive‐resistive exercise for the same time and frequency

Combined resistive leg cycling and upper‐extremity ergometry, four times per week for 6 weeks (4 h per week) 6 months 60 20 60 63 Low

Suputtitada et al. (2004)

Thailand Parallel arm RCT People who have stroke > 6 months prior to enrolment, are able to sit independently. BWSTT for seven times per week for 4 weeks (2.9 h per week) Overground walking, seven times per week for 4 weeks (2.9 h per week) NR 24 24 61 65 Some concerns

Takami and Wakayama 2010

Japan

Three‐arm parallel RCT

People who receive physical therapy, being able to walk 10 m unassisted

Group 1 received a control treatment six times a week for 3 weeks (3 h total) and also had treadmill training six times a week for 3 weeks (1 h total)

Group 2 received control intervention six times per week for 3 weeks (3 h per week) and additional body weight‐supported treadmill training in backward direction six times per week for 3 weeks (1 h per week)

CTL group received conventional physiotherapy including overground walking, six times per week for 3 weeks (4 h per week) plus ADL training five times per week for 3 weeks (3.3 h) 3 weeks 24 12 71 67

Some concerns

Toledano‐Zarhi et al. (2011) Israel Parallel arm RCT People with ischaemic stroke within 1 to 3 weeks before the trial Supervised exercise program including treadmill training twice per week for 6 weeks (180 min per week exercise training, including 70 to 110 min per week treadmill training) additionally to the control intervention Home exercise booklet with included instructions for flexibility and muscle strength exercises NR 14 14 65 65 Some concerns

Weng et al. (2004)

China Parallel arm RCT Comply with the Fourth National Stroke diagnostic criteria and able to walk more than 10 m Received five daily sessions of 20 min of body weight‐supported treadmill training for 4 weeks Received five daily sessions of 20 min conventional training for 4 weeks 4 weeks 25 25 55 55 High

Weng et al. (2006)

China Parallel arm RCT Comply with the Fourth National Stroke diagnostic criteria and able to walk more than 10 m Received five daily sessions of 30 min conventional training and 30 min of additional backward walking with body weight support on a treadmill for 3 weeks Received five daily sessions of 60 min conventional training for 3 week 3 weeks 13 13 51 50 Low

Werner et al. (2002)

Not mentioned Cross‐over RCT People whose age less than 75 years with first stroke and able to stand for at least 10 s Participants walked on a treadmill with partial body weight support provided by a harness Participants walked on a Gait Trainer with partial body weight support provided by a harness 6 weeks 15 15 NR NR Low

Yen et al. (2008)

Taiwan Parallel arm RCT Participants with unilateral stroke with unilateral hemiparesis, ≥ 6 months poststroke Group additionally to the control intervention, received 12 additional sessions of BWSTT, three times per week for 4 weeks (90 min per week) Group used general physiotherapy, two to five times per week for 4 weeks (100 to 250 min per week) 4 weeks 7 7 57 56 Low

Zhu et al. (2004)

China Parallel arm RCT People aged 30 to 80 years with ischaemic or haemorrhagic stroke are not able to walk. Participants walked on the Pneu‐weight system 5 sessions per week for 4 weeks (duration of sessions not stated), therapy (duration, body weight support) was tailored to the participants individual capabilities Conventional functional gait‐training 5 sessions per week for 4 weeks (duration of sessions not stated) 4 weeks 10 10 57 58 Some Concerns

Abbreviations: BWSTT, body weight‐supported treadmill training; C, control; I, intervention; m, metres; NR, not reported; RCT, randomized controlled trial; USA, United States of America.

3.3. Walking Speed

In the meta‐analysis, 57 studies involving 2895 participants were included, assessing the effects of treadmill training on walking speed in stroke survivors. The pooled SMD for overall effect was 0.255 (95% CI: 0.141 to 0.369), indicating a significant improvement in walking speed (z = 4.382, p < 0.001) when compared to control group (Figure 2). Heterogeneity was moderate with an I 2 of 49.3%, suggesting variability in study outcomes that could influence the interpretation of the effects.

FIGURE 2.

FIGURE 2

Forest plot showing the effectiveness of treadmill training in improving walking speed among patients with stroke.

Subgroup analysis based on the dependence of the participants at the time of recruitment revealed no significant effect in the dependent group (SMD = −0.004, 95% CI: −0.132 to 0.125), while significant improvement was noted in the independent group (SMD = 0.345, 95% CI: 0.207 to 0.484) (Figure 3). There was moderate heterogeneity in the independent group (I 2 = 51.3%) and minimal heterogeneity in the dependent group (I 2 = 0.0%). Subgroup analysis based on BWSTT combination revealed that the BWSTT subgroup (SMD = 0.316, 95% CI: 0.141 to 0.491) showed significant improvements in walking speed, contrasting the non‐BWSTT subgroup which exhibited minimal effect (SMD = 0.184, 95% CI: 0.051 to 0.318) (Figure 4). Publication bias assessment revealed asymmetrical funnel plot with significant Egger's test (p = 0.040) (Figure S1).

FIGURE 3.

FIGURE 3

Subgroup analysis based on dependency of the patients at the time of recruitment showing the effectiveness of treadmill training in improving walking speed among patients with stroke.

FIGURE 4.

FIGURE 4

Subgroup analysis based on body weight supported treadmill training showing the effectiveness of treadmill training in improving walking speed among patients withs stroke.

3.4. Walking Endurance

The meta‐analysis evaluated 38 studies with 2291 participants to assess the impact of treadmill training on walking endurance in stroke survivors. Pooled SMD was 0.277 (95% CI: 0.134 to 0.421), indicating a significant improvement in walking endurance (z = 3.780, p < 0.001) (Figure 5). However, there was moderate to high heterogeneity among the studies (I 2 = 58.9%), suggesting variation in the effects across different settings and populations.

FIGURE 5.

FIGURE 5

Forest plot showing the effectiveness of treadmill training in improving walking endurance among patients with stroke.

Subgroup analysis based on the dependence of the participants at the time of recruitment revealed that the independent subgroup (SMD = 0.374, 95% CI: 0.199 to 0.549) had significant improvements in walking endurance, contrasting with the dependent subgroup which demonstrated no significant effect (n = 38, SMD = −0.027, 95% CI: −0.166 to 0.111). High heterogeneity was observed in the independent group (I 2 = 58.4%) and minimal heterogeneity in the dependent group (I 2 = 0.0%). (Figure 6). Subgroup analysis based on BWSTT combination revealed that studies without BWSTT (SMD = 0.301, 95% CI: 0.086 to 0.516) and those with BWSTT (SMD = 0.259, 95% CI: 0.063 to 0.455) both demonstrated significant improvements in walking endurance, though the effect sizes were moderate. Moderate heterogeneity was observed within both subgroups (no BWSTT I 2 = 56.2%, yes BWSTT I 2 = 61.0%). (Figure 7). Publication bias assessment revealed asymmetrical funnel plot with significant Egger's test (p = 0.006) (Figure S2).

FIGURE 6.

FIGURE 6

Subgroup analysis based on dependency of the patients at the time of recruitment showing the effectiveness of treadmill training in improving walking endurance among patients with stroke.

FIGURE 7.

FIGURE 7

Subgroup analysis based on body weight supported treadmill training showing the effectiveness of treadmill training in improving walking endurance among patients with stroke.

4. Discussion

This comprehensive meta‐analysis encompassing 59 studies focused on the impact of treadmill training on walking speed and walking endurance among stroke survivors, yielding several significant insights. The overall pooled SMD for walking speed was 0.255 (95% CI: 0.141 to 0.369), indicating a substantial improvement. Similarly, for walking endurance, the pooled SMD was 0.277 (95% CI: 0.134 to 0.421), demonstrating notable gains. These findings affirm the efficacy of treadmill training in enhancing functional mobility poststroke.

Subgroup analyses added depth to these findings. For walking speed, participants who were independent at the start of treatment showed a significant improvement (SMD = 0.345, 95% CI: 0.207 to 0.484), while those who were dependent did not exhibit significant changes. This pattern was echoed in the walking endurance outcomes, where the independent subgroup showed substantial improvements (SMD = 0.374, 95% CI: 0.199 to 0.549) but the dependent group did not.

The analysis also highlighted the role of BWSTT, where both walking speed and endurance in groups that utilized BWSTT showed significant improvements compared to those that did not use this method. This suggests that BWSTT could be particularly beneficial in rehabilitation settings.

Publication bias was noted with significant Egger's test results (p = 0.040 for walking speed and p = 0.006 for walking endurance), indicating potential asymmetry in study reporting, which might influence the perceived effectiveness of treadmill training interventions.

The findings of this meta‐analysis are largely consistent with prior research, which has also identified treadmill training as a beneficial intervention for improving gait and endurance in stroke survivors. Studies such as those by Gelaw et al. 2019 and Bishnoi et al. 2022 have similarly reported improvements in walking speed and endurance following structured treadmill programs. However, the distinction between dependent and independent participants in relation to their response to the intervention provides new insights, suggesting that initial functional status is an important determinant of outcome success.

Previous literature has shown mixed results on the efficacy of BWSTT (Mehrholz et al. 2014; Mehrholz et al. 2017). While some studies report significant benefits, others find minimal differences when compared to conventional therapy (Bishnoi et al. 2022; Gelaw et al. 2019; Mehrholz et al. 2014; Mehrholz et al. 2017). Our findings support the notion that BWSTT adds value to the rehabilitation process, likely due to the enhanced safety and ability to initiate training earlier, which is crucial for capitalizing on the window of neuroplasticity soon after the stroke (Mehrholz et al. 2014; Mehrholz et al. 2017).

The significant improvements noted in independent participants align with the principle of “use it or lose it,” which is well‐documented in neurorehabilitation literature (Fasoli and Adans‐Dester 2019). Patients who are more active and retain some degree of functional independence prior to intervention typically experience greater gains due to their ability to engage more fully in therapeutic activities.

The mechanisms underlying the observed benefits of treadmill training in stroke rehabilitation can be attributed to several neurophysiological factors. Treadmill training promotes repetitive, rhythmic limb movements, which are thought to facilitate motor learning and neuroplasticity through the activation of CPGs in the spinal cord. This enhances the efficiency of neural pathways involved in walking, which is crucial for the recovery of functional mobility (Sun et al. 2013).

For BWSTT, the additional support allows patients, even those with severe impairments, to begin walking exercises sooner than they might otherwise. This early mobilization is critical as it helps to mitigate the effects of immobility and capitalizes on the early poststroke period when neuroplasticity is at its peak (Mehrholz et al. 2014; Mehrholz et al. 2017). In addition to facilitating earlier initiation of gait training and reducing fall risk, BWSTT provides a controlled environment that allows for prolonged, repetitive practice of proper gait cycles, which may enhance neuromuscular coordination and motor learning—factors that can directly contribute to improvements in gait speed and endurance (Mehrholz et al. 2014; Mehrholz et al. 2017). Furthermore, beyond the safety benefits, BWSTT enables precise adjustments of training parameters such as treadmill speed, duration and the level of body weight support, allowing therapists to tailor interventions that reinforce efficient gait patterns. This task‐specific, repetitive training environment is posited to promote both faster and more enduring improvements in walking performance, as supported by recent evidence (Mehrholz et al. 2014; Mehrholz et al. 2017). For patients with relatively preserved ambulatory function, treadmill training without BWSTT offers a beneficial challenge that promotes greater neuromuscular engagement and strength development, while BWSTT is primarily designed for those with severe impairments who require additional support for safe gait initiation.

The differential outcomes observed between dependent and independent groups may be explained by the varying degrees of motor and neural integrity within these populations. Independent individuals likely retain greater neural reserves and motor capabilities, enabling them to benefit more from the physical and neuroplastic challenges presented by treadmill training. Conversely, individuals who are more dependent may require more tailored interventions that address the specific deficits hindering their mobility (Zeller et al. 2024).

The strengths of this review lie in its comprehensive scope, including a large number of studies and participants, which provides a robust dataset for evaluating the effectiveness of treadmill training. The use of subgroup analyses to explore how different characteristics like initial dependency status and the use of BWSTT influence outcomes adds depth to the findings, offering practical insights for clinical practice.

However, the review is not without limitations. The significant heterogeneity observed across studies suggests variability in study design, participant characteristics, intervention protocols and outcome measures, which could affect the generalizability of the findings. The presence of publication bias also indicates that the results might be skewed towards studies showing positive outcomes, potentially overstating the effectiveness of treadmill training.

The evidence supports the incorporation of treadmill training, particularly BWSTT, into stroke rehabilitation programs, especially for patients who are not severely disabled. Rehabilitation professionals should consider the initial functional status of stroke survivors when designing and implementing treadmill training programs to maximize recovery outcomes. The findings also underscore the importance of early intervention to exploit the window of heightened neuroplasticity poststroke.

Further analysis of our results suggests that the differential outcomes observed between independent and dependent patients may reflect underlying variations in neuromuscular capacity and the ability to engage in repetitive gait training. Independent stroke survivors, who generally have higher residual motor function at baseline, appear better positioned to benefit from the repetitive, rhythmic nature of treadmill training. This may lead to enhanced motor learning and neuroplastic adaptations, thereby facilitating more substantial improvements in walking speed and endurance.

The use of BWSTT further accentuates these effects by enabling safe early mobilization, particularly in patients who may be at risk of falls. BWSTT appears to provide the necessary support that allows patients, especially those with moderate impairments, to practice gait training more intensively and with reduced fear of injury. However, our findings indicate that while BWSTT can enhance walking outcomes, its benefits are more pronounced in individuals with some baseline degree of independence. In contrast, patients classified as dependent—those requiring significant physical assistance or reliance on assistive devices—showed minimal improvement. This suggests that for these patients, additional or alternative rehabilitation strategies (e.g., robotics, targeted strength and balance interventions) may be required to address more severe deficits.

Inference from these observations underscores the importance of tailoring treadmill training interventions based on baseline functional status. Clinicians should consider incorporating BWSTT to maximize early functional gains in patients who are moderately impaired while exploring complementary approaches for those with greater dependency. Future research should aim to refine standardized protocols that adapt treadmill training modalities according to patient‐specific needs, ultimately optimizing the potential for functional recovery poststroke.

5. Conclusion

This meta‐analysis underscores the efficacy of treadmill training in improving walking speed and endurance among stroke survivors, with notable benefits particularly for those who are independent during study recruitment. The incorporation of BWSTT appears to enhance these benefits, making it a valuable component of comprehensive stroke rehabilitation programs. Despite the challenges posed by heterogeneity and publication bias, the evidence strongly supports the role of treadmill training in enhancing poststroke recovery, meriting its inclusion in clinical practice and further exploration in research.

Author Contributions

All the authors were involved in conception and design of the study, screening, data collection and analysis, writing the first draft, critical appraisal of the article and approval of the final version of the manuscript.

Ethics Statement

The authors have nothing to report.

Conflicts of Interest

The authors declare no conflicts of interest.

Supporting information

Appendix S1 Supporting Information.

IJN-31-e70020-s001.pdf (95.2KB, pdf)

Figure S1 Funnel plot for walking speed.

IJN-31-e70020-s002.jpg (478.5KB, jpg)

Figure S2 Funnel plot for walking endurance.

IJN-31-e70020-s003.jpg (457.9KB, jpg)

Acknowledgements

The authors have nothing to report.

Funding: The authors received no specific funding for this work.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

References

  1. Ada, L. , Dean C., and Lindley R.. 2013. “Randomized Trial of Treadmill Training to Improve Walking in Community‐Dwelling People After Stroke: The Ambulate Trial.” International Journal of Stroke 8, no. 6: 436–444. [DOI] [PubMed] [Google Scholar]
  2. Ada, L. , Dean C. M., Hall J. M., Bampton J., and Crompton S.. 2003. “A Treadmill and Overground Walking Program Improves Walking in Persons Residing in the Community After Stroke: A Placebo‐Controlled, Randomized Trial.” Archives of Physical Medicine and Rehabilitation 84, no. 10: 1486–1491. [DOI] [PubMed] [Google Scholar]
  3. Aguiar, L. T. , Nadeau S., Britto R. R., et al. 2020. “Effects of Aerobic Training on Physical Activity in People With Stroke: A Randomized Controlled Trial.” NeuroRehabilitation 46: 391–401. [DOI] [PubMed] [Google Scholar]
  4. Baek, C. Y. , Chang W. N., Park B. Y., Lee K. B., Kang K. Y., and Choi M. R.. 2021. “Effects of Dual‐Task Gait Treadmill Training on Gait Ability, Dual‐Task Interference, and Fall Efficacy in People With Stroke: A Randomized Controlled Trial.” Physical Therapy 101, no. 6: pzab067. [DOI] [PubMed] [Google Scholar]
  5. Bishnoi, A. , Lee R., Hu Y., Mahoney J. R., and Hernandez M. E.. 2022. “Effect of Treadmill Training Interventions on Spatiotemporal Gait Parameters in Older Adults With Neurological Disorders: Systematic Review and Meta‐Analysis of Randomized Controlled Trials.” International Journal of Environmental Research and Public Health 19, no. 5: 2824. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Boehme, C. , Toell T., Lang W., and Knoflach M.. 2021. “Longer Term Patient Management Following Stroke: A Systematic Review.” International Journal of Stroke 16, no. 8: 917–926. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Bonnyaud, C. , Pradon D., Zory R., Bensmail D., Vuillerme N., and Roche N.. 2013a. “Does a Single Gait Training Session Performed Either Overground or on a Treadmill Induce Specific Short‐Term Effects on Gait Parameters in Patients With Hemiparesis? A Randomized Controlled Study.” Topics in Stroke Rehabilitation 20: 509–518. [DOI] [PubMed] [Google Scholar]
  8. Bonnyaud, C. , Pradon D., Zory R., Bussel B., Bensmail D., and Vuillerme N.. 2013b. “Effects of a Gait Training Session Combined With a Mass on the Non‐Paretic Lower Limb on Locomotion of Hemiparetic Patients: A Randomized Controlled Clinical Trial.” Gait & Posture 37: 627–630. [DOI] [PubMed] [Google Scholar]
  9. Brauer, S. G. , Kuys S. S., Ada L., and Paratz J. D.. 2022. “Improving Physical Activity After Stroke via Treadmill Training (IMPACT) and Self‐Management: A Randomized Trial.” International Journal of Stroke 17: 1137–1144. [DOI] [PubMed] [Google Scholar]
  10. Cakmak, E. T. , Yaliman A., Torna G., and Sen E. I.. 2024. “The Effectiveness of Bodyweight‐Supported Treadmill Training in Stroke Patients: Randomized Controlled Trial.” Neurological Sciences 45: 3277–3285. 10.1007/s10072-024-07385-z. [DOI] [PubMed] [Google Scholar]
  11. Combs‐Miller, S. A. , Kalpathi P. A., Colburn D., et al. 2014. “Body Weight‐Supported Treadmill Training vs. Overground Walking Training for Persons With Chronic Stroke: A Pilot Randomized Controlled Trial.” Clinical Rehabilitation 28: 873–884. [DOI] [PubMed] [Google Scholar]
  12. Cumpston, M. , Li T., Page M. J., et al. 2019. “Updated Guidance for Trusted Systematic Reviews: A New Edition of the Cochrane Handbook for Systematic Reviews of Interventions.” Cochrane Database of Systematic Reviews 2019, no. 10: 1–2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Da Cunha Filho, I. T. , Lim P. A., Qureshy H., Henson H., Monga T., and Protas E. J.. 2002. “Gait Outcomes After Acute Stroke Rehabilitation With Supported Treadmill Ambulation Training: A Randomized Controlled Pilot Study.” Archives of Physical Medicine and Rehabilitation 83, no. 9: 1258–1265. [DOI] [PubMed] [Google Scholar]
  14. Damiano, D. L. , and DeJong S. L.. 2009. “A Systematic Review of the Effectiveness of Treadmill Training and Body Weight Support in Pediatric Rehabilitation.” Journal of Neurologic Physical Therapy 33, no. 1: 27–44. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Deniz, L. , Armagan O., Ozgen M., and Oner S.. 2011. “Effectiveness of Gait Training With Partial Body‐Weight Support in Subacute Stroke Patients.” Turkish Journal of Cerebrovascular Diseases 17, no. 1: 13–19. [Google Scholar]
  16. DePaul, V. G. , Wishart L. R., Richardson J., Thabane L., Ma J., and Lee T. D.. 2015. “Varied Overground Walking Training Versus Body‐Weight‐Supported Treadmill Training in Adults Within 1 Year of Stroke: A Randomized Controlled Trial.” Neurorehabilitation and Neural Repair 29: 329–340. [DOI] [PubMed] [Google Scholar]
  17. Duncan, P. W. , Sullivan K. J., Behrman A. L., et al. 2011. “Body‐Weight‐Supported Treadmill Rehabilitation After Stroke.” New England Journal of Medicine 364, no. 21: 2026–2036. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Eich, H. J. , Mach H., Werner C., and Hesse S.. 2004. “Aerobic Treadmill Plus Bobath Walking Training Improves Walking in Subacute Stroke: A Randomised Controlled Trial.” Clinical Rehabilitation 18: 640–651. [DOI] [PubMed] [Google Scholar]
  19. Elendu, C. , Amaechi D. C., Elendu T. C., et al. 2023. “Stroke and Cognitive Impairment: Understanding the Connection and Managing Symptoms.” Annals of Medicine and Surgery 85, no. 12: 6057–6066. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Fasoli, S. E. , and Adans‐Dester C. P.. 2019. “A Paradigm Shift: Rehabilitation Robotics, Cognitive Skills Training, and Function After Stroke.” Frontiers in Neurology 10: 1088. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Franceschini, M. , Carda S., Agosti M., Antenucci R., Malgrati D., and Cisari C.. 2009. “Walking After Stroke: What Does Treadmill Training With Body Weight Support Add to Overground Gait Training in Patients Early After Stroke? A Single‐Blind, Randomized, Controlled Trial.” Stroke 40, no. 9: 3079–3085. [DOI] [PubMed] [Google Scholar]
  22. Gama, G. L. , Celestino M. L., Barela J. A., Forrester L., Whittal J., and Barela A. M.. 2017. “Effects of Gait Training With Body Weight Support on a Treadmill Versus Overground in Individuals With Stroke.” Archives of Physical Medicine and Rehabilitation 98, no. 4: 738–745. [DOI] [PubMed] [Google Scholar]
  23. Gelaw, A. Y. , Janakiraman B., Teshome A., and Ravichandran H.. 2019. “Effectiveness of Treadmill Assisted Gait Training in Stroke Survivors: A Systematic Review and Meta‐Analysis.” Global Epidemiology 1: 100012. [Google Scholar]
  24. Globas, C. , Becker C., Cerny J., et al. 2011. “Chronic Stroke Survivors Benefit From High‐Intensity Aerobic Treadmill Exercise: A Randomized Controlled Trial.” Neurorehabilitation and Neural Repair 26, no. 1: 85–95. [DOI] [PubMed] [Google Scholar]
  25. Harvey, R. L. 2009. “Improving Poststroke Recovery: Neuroplasticity and Task‐Oriented Training.” Current Treatment Options in Cardiovascular Medicine 11, no. 3: 251–259. [DOI] [PubMed] [Google Scholar]
  26. Hornby, T. G. , Campbell D. D., Kahn J. H., Demott T., Moore J. L., and Roth H. R.. 2008. “Enhanced Gait‐Related Improvements After Therapist‐ Versus Robotic‐Assisted Locomotor Training in Subjects With Chronic Stroke: A Randomized Controlled Study.” Stroke 39, no. 6: 1786–1792. [DOI] [PubMed] [Google Scholar]
  27. Hornby, T. G. , Henderson C. E., Plawecki A., et al. 2019. “Contributions of Stepping Intensity and Variability to Mobility in Individuals Poststroke.” Stroke 50: 2492–2499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Hoyer, E. , Jahnsen R., Stanghelle J. K., and Strand L. I.. 2012. “Body Weight Supported Treadmill Training Versus Traditional Training in Patients Dependent on Walking Assistance After Stroke: A Randomized Controlled Trial.” Disability and Rehabilitation 34, no. 3: 210–219. [DOI] [PubMed] [Google Scholar]
  29. Jaffe, D. L. , Brown D. A., Pierson‐Carey C. D., Buckley E. L., and Lew H. L.. 2004. “Stepping Over Obstacles to Improve Walking in Individuals With Poststroke Hemiplegia.” Journal of Rehabilitation Research and Development 41, no. 3A: 283–292. [DOI] [PubMed] [Google Scholar]
  30. Kang, H.‐K. , Kim Y., Chung Y., and Hwang S.. 2012. “Effects of Treadmill Training With Optic Flow on Balance and Gait in Individuals Following Stroke: Randomized Controlled Trials.” Clinical Rehabilitation 26, no. 3: 246–255. [DOI] [PubMed] [Google Scholar]
  31. Kaźmierczak, K. , Wareńczak‐Pawlicka A., Miedzyblocki M., and Lisiński P.. 2022. “Effect of Treadmill Training With Visual Biofeedback on Selected Gait Parameters in Subacute Hemiparetic Stroke Patients.” International Journal of Environmental Research and Public Health 19, no. 24: 16925. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Kelley, C. P. , Childress J., Boake C., and Noser E. A.. 2013. “Over‐Ground and Robotic‐Assisted Locomotor Training in Adults With Chronic Stroke: A Blinded Randomized Clinical Trial.” Disability and Rehabilitation. Assistive Technology 8, no. 2: 161–168. 10.3109/17483107.2012.720242. [DOI] [PubMed] [Google Scholar]
  33. Khaku, A. S. , and Tadi P.. 20232024. “Cerebrovascular Disease.” In StatPearls [Internet]. StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK430927/. [PubMed] [Google Scholar]
  34. Kim, C. , Gong W., and Kim S.. 2011. “The Effects of Lower Extremity Muscle Strengthening Exercise and Treadmill Walking Exercise on the Gait and Balance of Stroke Patients.” Journal of Physical Therapy Science 23, no. 3: 405–408. [Google Scholar]
  35. Kim, J. , and Yim J.. 2017. “Effects of an Exercise Protocol for Improving Handgrip Strength and Walking Speed on Cognitive Function in Patients With Chronic Stroke.” Medical Science Monitor 23: 5402–5409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Kim, N. , Lee B. H., Kim Y., and Min W.. 2016. “Effects of Virtual Reality Treadmill Training on Community Balance Confidence and Gait in People Post‐Stroke: A Randomized Controlled Trial.” Journal of Experimental Stroke and Translational Medicine 9: 1–7. [Google Scholar]
  37. Kosak, M. C. , and Reding M. J.. 2000. “Comparison of Partial Body Weight‐Supported Treadmill Gait Training Versus Aggressive Bracing Assisted Walking Post Stroke.” Neurorehabilitation and Neural Repair 14, no. 1: 13–19. [DOI] [PubMed] [Google Scholar]
  38. Kuys, S. S. , Brauer S. G., and Ada L.. 2011. “Higher‐Intensity Treadmill Walking During Rehabilitation After Stroke Is Feasible and Not Detrimental to Walking Pattern or Quality: A Pilot Randomized Trial.” Clinical Rehabilitation 25, no. 4: 316–326. [DOI] [PubMed] [Google Scholar]
  39. Langhammer, B. , and Stanghelle J. K.. 2010. “Exercise on a Treadmill or Walking Outdoors? A Randomized Controlled Trial Comparing Effectiveness of Two Walking Exercise Programmes Late After Stroke.” Clinical Rehabilitation 24, no. 1: 46–54. [DOI] [PubMed] [Google Scholar]
  40. Laufer, Y. , Dickstein R., Chefez Y., and Marcovitz E.. 2001. “The Effect of Treadmill Training on the Ambulation of Stroke Survivors in the Early Stages of Rehabilitation: A Randomized Study.” Journal of Rehabilitation Research and Development 38, no. 1: 69–78. [PubMed] [Google Scholar]
  41. Liston, R. , Mickelborough J., Harris B., Hann A. W., and Tallis R. C.. 2000. “Conventional Physiotherapy and Treadmill Re‐Training for Higher‐Level Gait Disorders in Cerebrovascular Disease.” Age and Ageing 29, no. 4: 311–318. [DOI] [PubMed] [Google Scholar]
  42. Luft, A. R. , Macko R. F., Forrester L. W., et al. 2008. “Treadmill Exercise Activates Subcortical Neural Networks and Improves Walking After Stroke: A Randomized Controlled Trial.” Stroke 39, no. 12: 3341–3350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Mackay‐Lyons, M. , McDonald A., Matheson J., Eskes G., and Klus M. A.. 2013. “Dual Effects of Body‐Weight Supported Treadmill Training on Cardiovascular Fitness and Walking Ability Early After Stroke: A Randomized Controlled Trial.” Neurorehabilitation and Neural Repair 27, no. 7: 644–653. [DOI] [PubMed] [Google Scholar]
  44. Macko, R. F. , Ivey F. M., Forrester L. W., et al. 2005. “Treadmill Exercise Rehabilitation Improves Ambulatory Function and Cardiovascular Fitness in Patients With Chronic Stroke: A Randomized, Controlled Trial.” Stroke 36, no. 10: 2206–2211. [DOI] [PubMed] [Google Scholar]
  45. Mao, Y. R. , Lo W. L., Lin Q., et al. 2015. “The Effect of Body Weight Support Treadmill Training on Gait Recovery, Proximal Lower Limb Motor Pattern, and Balance in Patients With Subacute Stroke.” BioMed Research International 2015: 175719. 10.1155/2015/175719. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. McCain, K. J. , Pollo F. E., Baum B. S., et al. 2008. “Locomotor Treadmill Training With Partial Body‐Weight Support Before Overground Gait in Adults With Acute Stroke: A Pilot Study.” Archives of Physical Medicine and Rehabilitation 89, no. 4: 684–691. [DOI] [PubMed] [Google Scholar]
  47. Mehrholz, J. , Pohl M., and Elsner B.. 2014. “Treadmill Training and Body Weight Support for Walking After Stroke.” Cochrane Database of Systematic Reviews 2014, no. 1: CD002840. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Mehrholz, J. , Thomas S., and Elsner B.. 2017. “Treadmill Training and Body Weight Support for Walking After Stroke.” Cochrane Database of Systematic Reviews 2017, no. 8: CD002840. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Middleton, A. , Merlo‐Rains A., Peters D. M., et al. 2014. “Body Weight‐Supported Treadmill Training Is No Better Than Overground Training for Individuals With Chronic Stroke: A Randomized Controlled Trial.” Topics in Stroke Rehabilitation 21: 462–476. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Moore, J. L. , Roth E. J., Killian C., and Hornby T. G.. 2010. “Locomotor Training Improves Daily Stepping Activity and Gait Efficiency in Individuals Poststroke Who Have Reached a "Plateau" in Recovery.” Stroke 41, no. 1: 129–135. [DOI] [PubMed] [Google Scholar]
  51. Nave, A. H. , Rackoll T., Grittner U., et al. 2019. “Physical Fitness Training in Patients With Subacute Stroke (PHYS‐STROKE): Multicentre, Randomised Controlled, Endpoint Blinded Trial.” BMJ 366: l5101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Nilsson, L. , Carlsson J., Danielsson A., et al. 2001. “Walking Training of Patients With Hemiparesis at an Early Stage After Stroke: A Comparison of Walking Training on a Treadmill With Body Weight Support and Walking Training on the Ground.” Clinical Rehabilitation 15, no. 5: 515–527. [DOI] [PubMed] [Google Scholar]
  53. Olawale, O. A. , Jaja S. I., Anigbogu C. N., et al. 2009. “Effects of Two Exercise Training Techniques on Walking Function in Adult Patients With Stroke.” Nigerian Quarterly Journal of Hospital Medicine 19, no. 2: 88–94. [PubMed] [Google Scholar]
  54. Park, I. M. , Lee Y. S., Moon B. M., and Sim S. M.. 2013. “A Comparison of the Effects of Overground Gait Training and Treadmill Gait Training According to Stroke Patients' Gait Velocity.” Journal of Physical Therapy Science 25: 379–382. [Google Scholar]
  55. Park, J. , Park S.‐Y., Kim Y.‐W., and Woo Y.. 2015. “Comparison Between Treadmill Training With Rhythmic Auditory Stimulation and Ground Walking With Rhythmic Auditory Stimulation on Gait Ability in Chronic Stroke Patients: A Pilot Study.” NeuroRehabilitation 37: 193–202. [DOI] [PubMed] [Google Scholar]
  56. Pohl, M. , Mehrholz J., Ritschel C., and Ruckriem S.. 2002. “Speed‐Dependent Treadmill Training in Ambulatory Hemiparetic Stroke Patients: A Randomized Controlled Trial.” Stroke 33: 553–558. [DOI] [PubMed] [Google Scholar]
  57. Ribeiro, T. , Britto H., Oliveira D., Silva E., Galvao E., and Lindquist A.. 2013. “Effects of Treadmill Training With Partial Body Weight Support and the Proprioceptive Neuromuscular Facilitation Method on Hemiparetic Gait: A Randomized Controlled Study.” European Journal of Physical and Rehabilitation Medicine 49: 451–461. [PubMed] [Google Scholar]
  58. Richards, C. L. , Malouin F., Bravo G., Dumas F., and Wood‐Dauphinee S.. 2004. “The Role of Technology in Task‐Oriented Training in Persons With Subacute Stroke: A Randomized Controlled Trial.” Neurorehabilitation and Neural Repair 18, no. 4: 199–211. [DOI] [PubMed] [Google Scholar]
  59. Richards, C. L. , Malouin F., Wood‐Dauphinee S., Williams J. I., Bouchard J. P., and Brunet D.. 1993. “Task‐Specific Physical Therapy for Optimization of Gait Recovery in Acute Stroke Patients.” Archives of Physical Medicine and Rehabilitation 74, no. 6: 612–620. [DOI] [PubMed] [Google Scholar]
  60. Serra, M. C. , Hafer‐Macko C. E., Robbins R., O'Connor J. C., and Ryan A. S.. 2022. “Randomization to Treadmill Training Improves Physical and Metabolic Health in Association With Declines in Oxidative Stress in Stroke.” Archives of Physical Medicine and Rehabilitation 103, no. 11: 2077–2084. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Srivastava, A. , Taly A. B., Gupta A., Kumar S., and Murali T.. 2016. “Body‐Weight‐Supported Treadmill Training for Retraining Gait Among Chronic Stroke Survivors: A Randomized Controlled Study.” Annals of Physical and Rehabilitation Medicine 59: 235–241. [DOI] [PubMed] [Google Scholar]
  62. Sterne, J. A. , Savović J., Page M. J., et al. 2019. “RoB 2: A Revised Tool for Assessing Risk of Bias in Randomised Trials.” BMJ 366: l4898. [DOI] [PubMed] [Google Scholar]
  63. Sullivan, K. J. , Brown D. A., Klassen T., et al. 2007. “Effects of Task‐Specific Locomotor and Strength Training in Adults who Were Ambulatory After Stroke: Results of the Steps Randomized Clinical Trial.” Physical Therapy 87, no. 12: 1580–1602. 10.2522/ptj.20060310. [DOI] [PubMed] [Google Scholar]
  64. Sun, T. , Ye C., Wu J., Zhang Z., Cai Y., and Yue F.. 2013. “Treadmill Step Training Promotes Spinal Cord Neural Plasticity After Incomplete Spinal Cord Injury.” Neural Regeneration Research 8, no. 27: 2540–2547. 10.3969/j.issn.1673-5374.2013.27.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. Suputtitada, A. , Yooktanan P., and Rarerng‐Ying T.. 2004. “Effect of Partial Body Weight Support Treadmill Training in Chronic Stroke Patients.” Chotmaihet Thangphaet 87, no. Suppl 2: S107–S111. [PubMed] [Google Scholar]
  66. Takami, A. , and Wakayama S.. 2010. “Effects of Partial Body Weight Support While Training Acute Stroke Patients to Walk Backwards on a Treadmill ‐ A Controlled Clinical Trial Using Randomized Allocation.” Journal of Physical Therapy Science 22, no. 2: 177–187. [Google Scholar]
  67. Toledano‐Zarhi, A. , Tanne D., Carmeli E., and Katz‐Leurer M.. 2011. “Feasibility, Safety and Efficacy of an Early Aerobic Rehabilitation Program for Patients After Minor Ischemic Stroke: A Pilot Randomized Controlled Trial.” NeuroRehabilitation 28, no. 2: 85–90. [DOI] [PubMed] [Google Scholar]
  68. Weng, C. S. , Bi S., Tian Z., Yu Z. Z., Xu J., and Bi S. Q.. 2004. “Application of Structured Speed‐Dependent Treadmill Training in Hemiplegic Patients After Stroke.” Zhongguo Linchuang Kangfu 8, no. 34: 7617–7619. [Google Scholar]
  69. Weng, C. S. , Wang J., Pan X. Y., et al. 2006. “Effectiveness of Backward Walking Treadmill Training in Lower Extremity Function After Stroke.” Zhonghua Yi Xue Za Zhi 86, no. 37: 2635–2638. [PubMed] [Google Scholar]
  70. Werner, C. , Von Frankenberg S., Treig T., Konrad M., and Hesse S.. 2002. “Treadmill Training With Partial Body Weight Support and an Electromechanical Gait Trainer for Restoration of Gait in Subacute Stroke Patients: A Randomized Crossover Study.” Stroke 33: 2895–2901. [DOI] [PubMed] [Google Scholar]
  71. Xiao, X. , Huang D., and O'Young B.. 2012. “Gait Improvement After Treadmill Training in Ischemic Stroke Survivors: A Critical Review of Functional MRI Studies.” Neural Regeneration Research 7, no. 31: 2457–2464. [DOI] [PMC free article] [PubMed] [Google Scholar]
  72. Yamamoto, R. , Sasaki S., Kuwahara W., and Hada T.. 2022. “Effect of Exoskeleton‐Assisted Body Weight‐Supported Treadmill Training on Gait Function for Patients With Chronic Stroke: A Scoping Review.” Journal of Neuroengineering and Rehabilitation 19: 143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  73. Yen, C. L. , Wang R. Y., Liao K. K., Huang C. C., and Yang Y. R.. 2008. “Gait Training Induced Change in Corticomotor Excitability in Patients With Chronic Stroke.” Neurorehabilitation and Neural Repair 22, no. 1: 22–30. [DOI] [PubMed] [Google Scholar]
  74. Zeller, D. , Hiew S., Odorfer T., and Nguemeni C.. 2024. “Considering the Response in Addition to the Challenge ‐ A Narrative Review in Appraisal of a Motor Reserve Framework.” Aging 16, no. 6: 5772–5791. [DOI] [PMC free article] [PubMed] [Google Scholar]
  75. Zhu, H. X. , Dou Z. L., Li K., Lan Y., and Hu X. Q.. 2004. “A Preliminary Investigation on the Correlation of Partial Body Weight Support Training With Hemiplegic Gait and Ambulation Function After Brain Injury.” Zhongguo Linchuang Kangfu 8, no. 25: 5205–5207. [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Appendix S1 Supporting Information.

IJN-31-e70020-s001.pdf (95.2KB, pdf)

Figure S1 Funnel plot for walking speed.

IJN-31-e70020-s002.jpg (478.5KB, jpg)

Figure S2 Funnel plot for walking endurance.

IJN-31-e70020-s003.jpg (457.9KB, jpg)

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.


Articles from International Journal of Nursing Practice are provided here courtesy of Wiley

RESOURCES