Virtual reality game boosts arm recovery in chronic stroke patients
NCT ID NCT07534124
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a non-immersive virtual reality system (MindMotion GO) could help people with chronic stroke improve arm function better than standard occupational therapy. Twenty-six adults who had a stroke more than 6 months ago participated in 8 weeks of training. The results will show if this fun, engaging approach can boost recovery and quality of life.
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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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26 people
The number who actually took part.
- Started
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Sep 2022
- Finished
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Aug 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: Participants must meet all of the following criteria: * Age between 18 and 80 years. * Chronic phase of ischemic stroke affecting the dominant hemisphere in the Middle Cerebral Artery territory (more than 6 months and less than 4 years since stroke onset). * Ability to actively extend the wrist at least 20 degrees and extend the fingers at least 10 degrees. * Upper limb muscle strength of the paretic limb ≥2 in the shoulder, elbow, and wrist. * Adequate trunk control. * Adequate vision and hearing to interact with the rehabilitation platform. * Ability to collaborate and follow study procedures. * Meeting safety criteria for Electroencephalography recording. * Signed informed consent. Exclusion Criteria: Participants will be excluded if any of the following conditions are present: * Severe cognitive impairment (Montreal Cognitive Assessment score \<10). * Major depression or emotional disorders associated with severe attention or cooperation deficits that may interfere with hand function. * Severe psychiatric disease. * Severe spasticity in the affected limb (Modified Modified Ashworth Scale ≥3-4). * Aphasia preventing comprehension of verbal instructions. * Visuospatial neglect preventing interaction with the rehabilitation interface. * Participation in other upper limb rehabilitation therapies during the study period. * Severe functional dependency prior to stroke. * History of other strokes occurring after the index stroke. * Any medical condition that, in the opinion of the investigator, could interfere with study participation or data interpretation.
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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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Complutense University of Madrid
Madrid, Madrid, Spain
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Brazilian version of a behavior change intervention to support healthy lifestyle adoption after stroke - iVIDAVC: protocol for a pilot randomized study
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