Clinical Trial

Hybrid Assistive Limb Application in Multiple Sclerosis Patients

Completed
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Summary
The Hybrid Assistive Limb (HAL) exoskeleton detects bioelectrical signals from the muscles, responds to the intention of voluntary movement, and provides biological feedback. In this study, the effects of HAL application on walking performance and balance in patients with multiple sclerosis will be examined in a single-center, controlled design. Participants will undergo walking rehabilitation with HAL for 1 hour per day, 5 days a week, for a total of 2 months. Walking and balance performance will be assessed before and after the intervention using the 10-Minute Walk Test (10MWT) to measure maximum walking speed, the 6-Minute Walk Test (6MWT) to evaluate walking endurance and cardiorespiratory performance, and the Timed Up and Go Test (TUG) to assess functional mobility and dynamic balance. Additionally, walking parameters and static balance will be measured using Tecnobody systems. Appropriate statistical tests will be applied, and a significance level of p\<0.05 will be considered.
Protocol Amendment History 2 changes
critical Trial status changed: Enrolling by Invitation → Completed 2026-07-08
notable Enrollment increased: 8 -> 13 participants 2026-07-08
Trial Details
NCT Number NCT07326852
Lead Sponsor Ege University
Conditions Multiple Sclerosis
Enrollment 13 participants
Start Date 2025-10-08
Primary Completion 2025-12-09 (estimated)
Study Completion 2026-02-09 (estimated)
Updated on ClinicalTrials.gov 2026-07-07