Virtual reality at home: a new hope for stroke recovery?
NCT ID NCT06392802
First seen Sep 03, 2026 · Last updated Sep 04, 2026 · Updated 1 time
Summary
This trial tests whether a home-based virtual reality rehabilitation program called Muvity can improve arm function, balance, and quality of life in people who had a stroke more than six months ago. Participants will be split into two groups: one doing the Muvity program at home and another receiving conventional rehabilitation. Researchers will measure changes in movement, balance, pain, and emotional well-being to see if the virtual reality approach is as effective or better than standard care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A home-based telerehabilitation program using the Muvity system, which provides non-immersive virtual reality exercises.
- What this could lead to
- If it works, this could offer stroke survivors a convenient, engaging way to continue rehabilitation at home, potentially improving arm function, balance, and quality of life while reducing the need for clinic visits.
- What could go wrong
- This is a small early-stage trial with only 39 participants, so results may not apply to everyone. The expected benefit is modest, and the program may not work as well as in-person therapy for some people.
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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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39 people
The number who actually took part.
- Started
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Mar 2023
- Finished
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Apr 2025
- 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 to 85 years
- 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: between 18 and 85 years old. * Stroke duration of more than six months + Discharge from post-stroke rehabilitation. * Moderate physical disability: scoring between 1-3 on the Modified Rankin Scale. * Standing: able to stand safely for 2 minutes without support (maximum score -4- on item 2 of the Berg Scale). * Vision: capable of correctly visualizing a screen at a distance of 2 meters. * Cognitive status: No cognitive impairment or mild cognitive impairment (Mini-Mental State Examination score ≥ 24). Ability to understand and follow verbal instructions in Catalan or Spanish. * Technological skills: capable of basic use of a mobile phone and computer (keyboard, mouse, screen). * Glenohumeral joint mobility: minimum of 30º flexion, abduction, horizontal abduction; and 15º internal and external rotation. * Elbow joint mobility: minimum of 45º flexion. Exclusion Criteria: * Engaging in intense physical therapies. * Severe aphasia: inability or difficulty communicating through speech. * Cognitive impairments affecting short and mid-term memory. * Vision: having visual deficits in either eye that may impair screen visualization. * Vision: experiencing hemispatial neglect, meaning difficulty processing stimuli on the side opposite to the injury.
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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.
Contacts and locations
Locations
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Associació Disminuïts Físics d'Osona
Vic, Barcelona, 08500, Spain
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Universitat Politècnica de Catalunya
Barcelona, Barcelona, 08019, Spain
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