Can video games help injured Babies' arms? new study tests VR therapy
NCT ID NCT07291310
First seen Jun 25, 2026 · Last updated Aug 05, 2026 · Updated 3 times
Summary
This study compares two rehabilitation approaches—virtual reality exercises and motor-cognitive dual-task training—in 14 children aged 7-14 with brachial plexus birth injury, a condition where arm nerves are damaged during birth. Each child will do their assigned program for 12 weeks, followed by a 9-month home program. Researchers will use brain scans (fMRI) and movement tests to see which approach better improves arm function and brain adaptation.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- virtual reality exercises and motor-cognitive dual-task exercises
- What this could lead to
- If successful, this could point toward better rehabilitation strategies that improve arm movement and brain adaptation in children with brachial plexus birth injury.
- What could go wrong
- This is a very small early study with only 14 children, so results may not apply to everyone. It compares two active treatments without a placebo, and long-term benefits are uncertain.
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
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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 14 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Jan 2029
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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7 to 14 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Children aged 7-14 years * Diagnosed with unilateral DBPP * C5-C6 or C5-C7 involvement (Narakas I, IIa, IIb) * Modified Pediatric Mini-Mental Scale score ≥26 * Child and parent willing to participate in the study Exclusion Criteria: * Previous nerve surgery for DBPP * Surgery within the past year or Botulinum Toxin injection within the past 3 months * Any neurological condition other than DBPP * Vision or hearing impairments affecting participation * Contraindications for fMRI * Fixed contractures in shoulder, elbow, wrist, or finger joints * Participation in regular physiotherapy or other rehabilitation programs within the past 3 months
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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
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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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Biruni University
Istanbul, Cevizlibağ, 34015, Turkey (Türkiye)
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