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Clinical Trials in Turkey / NCT07550270
Recruiting Not applicable

Body Weight-Supported and Virtual Reality Gait Training in Stroke Patients

NCT07550270 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-03-26
Last updated
2026-04-24

Condition(s) studied

StrokeWalking ImpairmentBalanceGait Training

Investigational drug(s) / intervention(s)

Virtual Reality-Assisted Gait TrainingBackward Gait TrainingForward Gait Training

Virtual Reality-Assisted Gait Training: Body weight-supported virtual reality-assisted forward gait training with 30% body weight support, applied five days per week for six weeks.

Backward Gait Training: Body weight-supported backward gait training with 30% body weight support, applied five days per week for six weeks.

Forward Gait Training: Body weight-supported forward gait training with 30% body weight support, applied five days per week for six weeks.

Study summary

The aim of this study is to compare the effects of body weight-supported gait training that includes virtual reality-assisted dual-task applications with body weight-supported forward and backward gait training on functional capacity, gait parameters (such as step length, gait speed, and balance), cognitive functions and psychological status in patients with stroke. The findings of this study are expected to contribute to the development of more effective rehabilitation strategies for improving mobility in patients with stroke

Eligibility

Sex
ALL
Min age
45 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Patients experiencing their first-ever stroke * Patients with a post-stroke duration of more than 2 weeks * Patients with plantar flexor muscle spasticity of the lower extremity less than grade 3 according to the Modified Ashworth Scale (MAS) * Patients with a Brunnstrom stage of the lower extremity greater than 2 * Patients who are able to stand independently or under supervision for at least 2 minutes for standing assessments * Patients who are able to walk at least 10 meters independently or under supervision, with or without an assistive device, for walking assessments * Patients with sufficient cognitive function to understand study instructions (Mini-Mental State Examination \[MMSE\] score \> 23) * Patients with stable medical and psychological conditions * Patients who are willing to participate in the study Exclusion Criteria: * Patients with bilateral hemispheric lesions * Patients with severe cardiovascular or musculoskeletal conditions that prevent walking (e.g., fixed ankle contracture) * Patients using a permanent urinary catheter, or those with pressure ulcers or urinary and/or fecal incontinence * Patients with unilateral neglect * Patients with neurological conditions other than stroke that may affect balance performance (e.g., Parkinson's disease, epilepsy, meningitis, cerebellar disorders, vertigo, dizziness, polyneuropathy) or musculoskeletal disorders (e.g., severe low back pain, knee disorders) * Patients with severe visual, hearing, or speech impairments

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ankara, Çankaya, Türkiye (Türkiye), 06800 Gaziler Physical Medicine and Rehabilitation Training And Research Hospital Ankara Çankaya Recruiting

More Gaziler Physical Medicine and Rehabilitation Education and Research Hospital trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07550270 on ClinicalTrials.gov ↗ ← All trials in Turkey