Can virtual piano lessons rewire the brain after stroke?
NCT ID NCT06366360
First seen Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time
Summary
After a stroke, some people develop unilateral spatial neglect, where they ignore one side of their body or surroundings. Researchers are testing whether an immersive virtual reality program that involves playing a virtual piano can improve this condition. Adults with stroke and spatial neglect join the study and are randomly assigned to either standard rehabilitation alone or standard rehabilitation plus the virtual reality music program for two weeks. The study measures changes in attention and daily activities before and after the program.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- an immersive virtual reality music practice program using the Piano Vision application
- What this could lead to
- If it works, this could offer stroke survivors with spatial neglect a more engaging rehabilitation option that uses sound and virtual space to retrain attention.
- What could go wrong
- The trial is small and early, so results may not hold up in larger groups. Virtual reality can cause dizziness or discomfort, and some patients may not tolerate or benefit from it.
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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 80 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2024
- Expected to finish
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Sep 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: * Men and women over 18 years * Free and informed written consent * Enrolled in the French social security system * Cerebral lesion of vascular origin * Unilateral spatial neglect syndrome Exclusion Criteria: * Epilepsy or migraine * Major vision problems * Major hearing impairment * Pre-existing cognitive impairment (MMSE \< 20) * Major disorders of verbal comprehension preventing the protocol * Refusal to sign consent form
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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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Hôpitaux de Saint-Maurice
RECRUITINGSaint-Maurice, 94410, France
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