Virtual reality rehab at home could transform stroke recovery
NCT ID NCT07240948
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a home-based virtual reality system (MUVITY) to help people who had a stroke 3-12 months ago improve their movement and quality of life. 322 participants will either use the VR system with remote therapist guidance or receive standard exercise instructions. The goal is to see if VR rehab boosts motor function, adherence, and well-being better than usual care.
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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 322 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Nov 2025
An estimate. Start dates often move.
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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.
Inclusion Criteria: * Age \>18 years-old * Ischemic or hemorrhagic stroke within 3 to 12 months before inclusion * Inclusion modified Rankin scale 1 to 3 * Motor rehabilitation requirements defined by the stroke neurologist/physiatrist in the out-patient clinic * Bipedal standing: capable of keeping on two feet for two minutes without using hand supports. Exclusion Criteria: * Technological abilities: patient and caregiver do not manage smartphone and computer * Severe aphasia/ language barrier with patient/caregiver that impairs communication * Severe cognitive impairment (dementia) that affects short- and medium-term memory. * End-of-life- or life-threatening pathology with an estimated survival \<1 year. * Receiving intense physical therapy (rehabilitation with at least one face-to-face physical treatment/week).
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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
1 site. 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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Hospital Universitari Vall d'Hebron
Barcelona, 08035, Spain
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Other studies related to the condition(s) this trial covers.
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