Fact CheckerSign in

NCT04855903Completed

Executive Functions Computerized Rehabilitation Using Virtual Reality to Improve Activities of Daily Living Post-stroke

Rehabilitation of Executive Functions in the Activities of the Daily Living of Chronic Post-stroke Patients: Using Virtual Reality and Computerized Rehabilitation to Simulate Real Environment for Rehabilitation.

Source: ClinicalTrials.gov · Last updated 28 Oct 2026

Brief summary (registry, in English)

This research aims to evaluate the effects of a cognitive reeducation carried out with the COVIRTUA Cognition software using a virtual environment, on real-life execution of activities of daily living (ADL) for patients with post-stroke dysexecutive disorders. We will assess patients' performances in achieving ADLs by the Goal Attainment Scaling (GAS) throughout the follow-up (3 months), based on the goals set at the beginning of management with each patient.

Status (registry)
Completed
Study type
Interventional
Enrollment
18 (actual)
First submitted
20 Apr 2021
Start date
21 Sept 2021
Primary completion date
5 Dec 2025
Lead sponsor
University Hospital, Toulouse
Diseases
Stroke
NCT number
NCT04855903

What you commit to

  • Study type: Interventional
  • Participants enrolled: 18
  • From 21 Sept 2021 to the primary completion date, 5 Dec 2025
  • 2 sites 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

  • Neurological pathology other than stroke or psychiatric disorder
  • Unstable epilepsy

Other

  • Pregnant women (clinical examination)
  • Alcohol and/or narcotics addiction
  • Major hearing deficit
  • Major visual deficit
  • Patient undergoing rehabilitation at a liberal therapist targeting executive functions during study time
  • Patient under safeguard of justice.
  • Patient simultaneously participating in another research study

Who the study is looking for

  • Vascular brain injury (stroke), in chronic phase (6 months or more after stroke), responsible for dysexecutive syndrome authenticated by the GREFEX/GRECO battery (Executive Function Evaluation Reflection Group)
  • Men and women over the age of 18
  • Presence of a caregiver
  • Social Security affiliation
  • Signing free and informed consent following clear and detailed information
  • Sufficient understanding of the French language to participate in the study

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

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

SiteCityCountrySite status
Centre de la Tour de Gassies
Coordinator of this site? Confirm its status
BrugesFranceUnknown status
University Hospital of Toulouse
Coordinator of this site? Confirm its status
ToulouseFranceUnknown status

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