Actively Recruiting

Phase Not Applicable
Age: 40Years - 84Years
All Genders
NCT07201974

Virtual Reality for Post-Stroke Gait Rehabilitation

Led by McGill University · Updated on 2026-03-20

40

Participants Needed

1

Research Sites

95 weeks

Total Duration

On this page

Sponsors

M

McGill University

Lead Sponsor

J

Jewish Rehabilitation Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to: (1) implement and test the feasibility of a new VR-ODT intervention offered as part of usual therapy time of patients with a sub-acute stoke; (2) explore the acceptability of the intervention from the perspective of clinicians and patients and; (3) implement measures to optimize the uptake and sustainability of the intervention within the clinical setting. Participants will engage in a personalized VR-ODT training for 4 weeks (2X 1hr/week) targeting six well-established community walking demands related to (1) walking speed and (2) distance; (3) postural transitions; (4) obstacle avoidance; (5) dual-task walking and; (6) a combination of demands 1-5. For each demand, patients will progress through levels of increasing difficulty according to personalized goals and success criteria.

CONDITIONS

Official Title

Virtual Reality for Post-Stroke Gait Rehabilitation

Who Can Participate

Age: 40Years - 84Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients referred by clinicians from inpatient and outpatient stroke rehabilitation programs at the Jewish Rehabilitation Hospital for mobility problems within 6 months
  • Aged between 40 and 74 years
  • Normal or corrected visual and auditory acuity
  • First-ever supratentorial unilateral stroke of 1 to 24 weeks duration
  • Ability to walk independently with or without walking aids for at least 1 minute at a speed of 0.4 to 0.9 meters per second
  • Intact or mildly affected cognitive function with MoCA scores 22 or higher out of 30
  • Intact to moderately affected visual-perceptual function with positive scores on up to 3 of 6 tasks on the Behavioural Inattention Test
Not Eligible

You will not qualify if you...

  • Comorbidities that interfere with walking
  • Comorbidities that interfere with visual perception
  • Lack of medical clearance for exercise

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Jewish Rehabilitation Hospital

Laval, Quebec, Canada, H7V1R2

Actively Recruiting

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Research Team

A

Anouk Lamontagne, PhD

CONTACT

M

Myriamn Villeneuve, Mec

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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