VR headset could boost stroke recovery at home
NCT ID NCT07202520
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a virtual reality device called H'Ability Home can help stroke survivors improve their independence and walking speed better than a standard paper exercise booklet. Forty-four people who have had a first stroke and are about to leave rehab will use the VR headset at home for six weeks, then compare results to six weeks of paper-based exercises. The goal is to see if the VR approach makes home rehab more effective.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- H'Ability Home virtual reality device
- What this could lead to
- If it works, this could offer a more engaging and effective way for stroke survivors to do rehab exercises at home, potentially improving their independence.
- What could go wrong
- This is a small early-stage trial with only 44 participants, so results may not apply to everyone. The device requires comfort with virtual reality, which may not suit all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 44 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2025
An estimate. Start dates often move.
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Patient Inclusion Criteria: * Stroke diagnosis: first stroke, with no history of stroke, documented in the medical record * Currently in rehabilitation (in a center) (full hospitalization or day hospitalization for at least 3 days/week) for another 2 to 4 weeks. * Planned return home (home self-rehabilitation phase): Patients at the end of their rehabilitation stay and scheduled to return home where the self-rehabilitation phase can take place. * Ability to use virtual reality: Physical and cognitive ability to interact with virtual reality devices, at the discretion of therapists. * Adult: Patients aged 18 years or older. * Informed consent: Voluntary agreement to participate in the study after a full explanation of its terms and conditions. * Member of a social security scheme or eligible beneficiary * Distance between home and center included within the usual perimeter of each site. * Presence of a third-party family caregiver at home who has agreed to ensure the patient's safety during self-rehabilitation sessions with the H'Ability Home device (consent) * Availability of a Wi-Fi network and internet access at the patient's home * Presence of an adequate space at home to perform rehabilitation exercises * Person with low to reasonable sensitivity to motion sickness (MSSQ ≤ 15) Patient non inclusion Criteria: * • Visual disorders incompatible with the use of virtual reality (absence of binocular vision, blindness, conjunctivitis, etc.) at the discretion of the investigator. PS: Visual disorders corrected by wearing a vision correction device are not concerned because glasses or contact lenses can be worn when using an IVR headset. * Major cognitive impairment: Severe cognitive impairment affecting the patient's ability to understand or follow study instructions, or to operate the device independently, at the investigators' discretion. * History of epilepsy: History of epileptic seizures, particularly photosensitive seizures, which may be triggered or aggravated by the use of virtual reality. * Medical instability: presence of unstable or uncontrolled medical conditions that could interfere with active participation in rehabilitation. * Psychiatric illnesses: active psychiatric disorders (e.g., psychosis, unstabilized bipolar disorder) that could disrupt participation and continuity of rehabilitation, at the investigators' discretion. * Wearing implantable medical devices or personal medical devices that could be affected by radio waves (pacemakers, cochlear implants, etc.) * Participation in another clinical study: engagement in another clinical study likely to interfere with the study objectives or outcome assessments * Planned hospitalization during the home self-rehabilitation period * Pregnant, childbirth, or breastfeeding women * Persons deprived of their liberty by a judicial (including guardianship, curatorship, and judicial protection) or administrative decision * Persons receiving psychiatric care or admitted to a health or social care facility for purposes other than research * Persons in an emergency situation unable to express their prior consent Third-party family caregiver Inclusion Criteria: * Adult: Person aged 18 years or older * Informed consent: Voluntary agreement to participate in the study after a full explanation of its terms and conditions. * Member of a social security scheme or entitled person * Patient's family caregiver * Ability to assist the patient in using the device * Ability to ensure the patient's safety when using the device * Agreement to assist and ensure the patient's safety when using the device at home * Agreement to provide feedback on the device by completing self-administered questionnaires (UTAUT) - optional Third-party family caregiver non-inclusion Criteria: * Pregnant, childbirth, or breastfeeding women * Persons deprived of their liberty by a judicial (including guardianship, curatorship, and judicial protection) or administrative decision * Persons receiving psychiatric care or admitted to a health or social care facility for purposes other than research * Persons in an emergency situation unable to express their prior consent
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
5 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Centre Mutualiste de Rééducation et de Réadaptation Fonctionnelles (CMRRF) de KERPAPE
Ploemeur, 56270, France
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Fondation Hopale - Centre de Jacques Calvé
Berck, 62600, France
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Fondation ILDYS - Centre de Perharidy
Roscoff, 29684, France
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Hôpital Léon Bérard
Hyères, 83418, France
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Pôle Saint Hélier
Rennes, 35043, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Moving patterns may help stroke survivors read faster
- Vibrating wearables put stroke walking to the test
- Robot plus electrical stimulation aims to rebuild arm movement after stroke
- Can a checklist and heart monitor stop repeat strokes?
- Heart hole or stroke trigger? global registry tracks who gets closure and what happens next