Actively Recruiting
Effect of Upper Extremity Support on Spatiotemporal Parameters of Gait in Individuals With Stroke
Led by Ankara Yildirim Beyazıt University · Updated on 2026-03-27
34
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Purpose: The primary goal of this study is to investigate how different levels of upper extremity (arm) support affect walking patterns in individuals who have experienced a stroke. Specifically, the research aims to determine how restricting or facilitating arm swing during walking modulates spatiotemporal gait parameters (such as speed, step length, and rhythm). Background: Arm swing plays a crucial role in maintaining balance, stability, and energy efficiency during normal walking. Following a stroke, many patients use walking aids (like canes or walkers) or clinical supports (like parallel bars) that restrict natural arm movement. This study examines whether these restrictions significantly alter gait mechanics in the stroke population. Methodology: Participants will participate in a cross-over experimental trial. Each participant will walk on a specialized treadmill system (C-Mill VR+) under three randomized conditions: 1. Unsupported walking (no arm support), 2. Single-arm support (using the non-paretic side), 3. Dual-arm support (using both arms). Researchers will record gait speed, step length, cadence, and duration of stance/swing phases for each condition. Expected Outcome: The findings will provide scientific evidence on how different support strategies modulate walking performance. This information will help physical therapists design more effective, individualized rehabilitation programs to improve mobility and quality of life for stroke survivors.
CONDITIONS
Official Title
Effect of Upper Extremity Support on Spatiotemporal Parameters of Gait in Individuals With Stroke
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of hemiplegia with ICD-10 code G.81
- Presence of unilateral hemiplegia
- No medical contraindications for the use of assistive devices such as cane or tripod
- Aged 18 years or older
- Ability to walk for at least 2 consecutive minutes
You will not qualify if you...
- Presence of aphasia
- Recurrent stroke
- Montreal Cognitive Assessment (MoCA) score below 10 points
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ankara Bilkent City Hospital
Ankara, Turkey (Türkiye), 06800
Actively Recruiting
Research Team
M
Murat AKINCI
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
BASIC_SCIENCE
Number of Arms
3
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