RecruitingNot ApplicableNCT07496853

Effect of Upper Extremity Support on Spatiotemporal Parameters of Gait in Individuals With Stroke

The Effect of Upper Extremity Support Usage on Spatiotemporal Gait Parameters in Individuals With Stroke: A Prospective Cross-over Experimental Study


Sponsor

Ankara Yildirim Beyazıt University

Enrollment

34 participants

Start Date

Apr 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Inclusion Criteria5

  • Diagnosis of hemiplegia with ICD-10 code G.81.
  • Presence of unilateral hemiplegia.
  • No medical contraindications for the use of assistive devices (e.g., cane, tripod).
  • Aged 18 years or older.
  • Ability to walk for at least 2 consecutive minutes.

Exclusion Criteria3

  • Presence of aphasia.
  • Recurrent stroke.
  • Montreal Cognitive Assessment (MoCA) score below 10 points.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DEVICEC-Mill VR+ (Force-plate integrated treadmill)

Description: A treadmill system equipped with integrated force plates and augmented reality (VR) capabilities. It records spatiotemporal gait data at a 500 Hz sampling frequency. In this study, the device is used to measure gait parameters under different upper extremity support conditions.

BEHAVIORALNo Support Protocol

The standardized protocol of walking under no support: Natural walking with free arm swing. Each trial lasts 2 minutes with mandatory rest periods to prevent fatigue.

BEHAVIORALUnilateral Support Protocol

The standardized protocol of walking under unilateral support: Holding the handrail with the non-paretic hand. Each trial lasts 2 minutes with mandatory rest periods to prevent fatigue.

BEHAVIORALBilateral Support Protocol

The standardized protocol of walking under bilateral support: Holding the handrails with both hands. Each trial lasts 2 minutes with mandatory rest periods to prevent fatigue.


Locations(1)

Ankara Bilkent City Hospital

Ankara, Turkey (Türkiye)

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07496853


Related Trials