Tolerance Study of Robotic-Assisted Virtual Reality Walking Rehabilitation for Non-Walking Stroke Patients

Recruiting N/A Interventional Study
Stroke Central Nervous System Diseases
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
35 – 75
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
30 (estimated)
Sponsor
University Hospital, Limoges · Other
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About This Trial
The primary objective of this study is to evaluate the tolerance of the use of immersive virtual reality (VR) during robotic walking rehabilitation sessions by Gait Trainer (GT) in post-stroke patients. Secondary objectives aim to evaluate the motivation to participate in VR sessions compared to conventional sessions, the participants' sense of presence within the virtual environment, and the usa…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Hemiparesis following a first ischemic or hemorrhagic stroke; * subacute phase (15 days to 6 months); * Aged 35 to 75 years; * Non-walking subject (unable to walk 3 x 10 meters without human assistance or Functional Ambulation Classification ≤ 2); * Benefiting from robot-assis…
Contacts

Maxence COMPAGNAT, MD

555056518

maxence.compagnat@chu-limoges.fr

CONTACT

Charles MORIZIO

charles.morizio@chu-limoges.fr

CONTACT