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NCT07201974Recruiting

Virtual Reality for Post-Stroke Gait Rehabilitation

iWalk in VR: Integration of Virtual Reality-based Locomotor Rehabilitation in Clinical Care

Source: ClinicalTrials.gov · Last updated 20 Mar 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
9 Sept 2025
Start date
1 Feb 2026
Primary completion date
30 Nov 2026
Lead sponsor
McGill University
Diseases
Stroke
NCT number
NCT07201974

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 1 Feb 2026 to the primary completion date, 30 Nov 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Lab values

  • Subjects without medical clearance for exercise

Other

  • Subjects with comorbidities interfering with walking
  • Subjects with comorbidities interfering with visual perception

Who the study is looking for

  • Eligible patients with stroke referred by clinicians of the inpatient and outpatient stroke rehabilitation programs at the Jewish Rehabilitation Hospital (CISSS Laval) for mobility problems over a period of 6 months will be recruited. They will:
  • be aged between 40 and 74 years;
  • have normal/corrected visual and auditory acuity present;
  • present a first-ever supratentorial unilateral stroke of 1-24 weeks duration;
  • present the ability to walk independently with/without walking aids for at least 1 min at a speed of 0.4-0.9 m/s;
  • present intact or mildly affected cognitive function (MoCA scores ≥ 22/30);
  • present intact to moderately affected visual- perceptual function (positive scores on a max. of 3/6 tasks on the Behavioural Inattention Test).

Age in the registry: 40 years to 84 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Jewish Rehabilitation Hospital
Coordinator of this site? Confirm its status
LavalCanadaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.