Virtual reality game boosts arm recovery in chronic stroke patients

NCT ID NCT07534124

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By invitation only
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Running, but no longer taking on new participants.
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Cancelled before anyone took part.

Expanded access (not trials)

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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.

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

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

26 people

The number who actually took part.

Started

Sep 2022

Finished

Aug 2025

Lead sponsor

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

18 to 85 years

Sex

Anyone

Healthy volunteers

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

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

  • Complutense University of Madrid

    Madrid, Madrid, Spain

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