NCT06053619Recruiting
Tolerance Study of Robotic-Assisted Virtual Reality Walking Rehabilitation for Non-Walking Stroke Patients
Source: ClinicalTrials.gov · Last updated 25 Jun 2026
Brief summary (registry, in English)
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 usability of the rehabilitation device created. Finally, we will report the actual walking time and number of steps stroke patients take in VR sessions and conventional sessions.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 30 (estimated)
- First submitted
- 19 Sept 2023
- Start date
- 20 Nov 2023
- Primary completion date
- 11 Mar 2027
- Lead sponsor
- University Hospital, Limoges
- Diseases
- Stroke
- NCT number
- NCT06053619
What you commit to
- Study type: Interventional
- Planned participants: 30
- From 20 Nov 2023 to the primary completion date, 11 Mar 2027
- 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.
Other illness
- Have neurological and psychiatric conditions, other than stroke;
- Conditions contraindicating the use of virtual reality (e.g., epileptic disorders, major cerebellar syndrome).
- Patient with acute cardiovascular and respiratory disorders;
- Person with high VR experience during the 5 years before stroke
Other
- Inability to evolve in a virtual environment (MSSQ-Short \> 26)
- Patient who is subject to a legal protection measure or who is unable to give consent;
- Person deprived of liberty
- pregnant woman, breastfeeding woman
Who the study is looking for
- 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-assisted walking rehabilitation in the readaptation and physical medecin department of the Limoges University Hospital;
- Having the cognitive abilities to understand and follow simple verbal instructions (MMSE \< 24 or BDAE \< 2)
- Be able to give informed consent to participate in this study.
Age in the registry: 35 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU de Limoges Coordinator of this site? Confirm its status | Limoges | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.