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Clinical Trials in Turkey / NCT07471919
Recruiting Not applicable

Robot-Assisted Gait Training vs Visual Feedback Balance Training in Stroke

NCT07471919 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-03-15
Last updated
2026-08-19

Condition(s) studied

StrokeGait ImpairmentBalance Impairment

Investigational drug(s) / intervention(s)

Robot-Assisted Gait TrainingVisual Feedback Balance Training

Robot-Assisted Gait Training: Robot-Assisted Gait Training (RoboGait®) Robot-assisted gait training will be delivered using the RoboGait® device (Bama Technology, METU Technokent, Ankara, Türkiye). The system provides repetitive, task-specific gait training with controlled movement patterns to improve dynamic balance, gait symmetry, and motor relearning. Sessions will be performed twice weekly for 4 weeks, each lasting 30 minutes. Body weight support and gait parameters will be adjusted according to the patient's clinical status and tolerance. Other: Conventional Rehabilitation Program All participants will receive conventional rehabilitation for 40 minutes per session, 5 days per week for 4 weeks. The program includes static and dynamic balance exercises, lower extremity and trunk strengthening, weight shifting, sit-to-stand training, turning activities, and gait-related balance exercises under therapist supervision. Exercise progression will be individualized based on functional capacity and safety.

Visual Feedback Balance Training: Visual Feedback Balance Training Visual feedback balance training will be performed using the ProKin 252 system (TecnoBody S.R.L., Bergamo, Italy). The system provides real-time visual feedback to improve postural stability, weight shifting, and dynamic balance control. Sessions will be conducted twice weekly for 4 weeks, each lasting 30 minutes. Training difficulty will be progressively adjusted according to patient performance and safety. Other: Conventional Rehabilitation Program All participants will receive conventional rehabilitation for 40 minutes per session, 5 days per week for 4 weeks. The program includes static and dynamic balance exercises, lower extremity and trunk strengthening, weight shifting, sit-to-stand training, turning activities, and gait-related balance exercises under therapist supervision. Exercise progression will be individualized based on functional capacity and safety.

Study summary

Stroke frequently leads to balance impairment and gait dysfunction, increasing fall risk and limiting functional independence. Technology-assisted rehabilitation approaches such as robot-assisted gait training and visual feedback balance training have been shown to improve balance and mobility in stroke patients.

This randomized, assessor-blinded clinical trial aims to compare the effects of robot-assisted gait training and visual feedback balance training on balance and gait outcomes in patients with subacute and chronic stroke. Both interventions are part of routine clinical rehabilitation practice. Participants will be evaluated at baseline and after 4 weeks of intervention using clinical balance, gait, and functional assessments.

Eligibility

Sex
ALL
Min age
21 Years
Max age
85 Years
Healthy volunteers
No
Inclusion Criteria: * Age 21-85 years * Diagnosis of ischemic or hemorrhagic stroke confirmed by clinical and radiological findings * Functional Ambulation Category (FAC) ≥ 3 * Modified Ashworth Scale ≤ 2 (lower extremity) * Ability to understand and follow simple verbal instructions * Mini-Mental State Examination (MMSE) score ≥ 23 Exclusion Criteria: * Unstable cardiopulmonary conditions * Severe musculoskeletal disorders affecting standing or walking * Severe aphasia preventing participation in assessments * Severe visual impairment interfering with balance testing

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
AIBU Izzet Baysak Physical Treatment and Rehabilitation Hospital Bolu Turkey (Türkiye) Recruiting

More Abant Izzet Baysal University trials in Turkey

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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 NCT07471919 on ClinicalTrials.gov ↗ ← All trials in Turkey