AI reads Kids' body signals to improve rehab sessions
NCT ID NCT06993389
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether an AI model could predict how children with movement problems engage with rehabilitation. Researchers collected heart activity, sweat response, and movement data from 31 children during therapy sessions. The goal is to help therapists adjust treatments in real-time for better, more personalized care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help therapists personalize rehabilitation sessions in real-time for children with movement difficulties.
- What could go wrong
- This is a small, completed observational study with only 31 participants. The AI model needs further testing in larger trials before it can be used in clinics.
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.
- Participants
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31 people
The number who actually took part.
- Started
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Jun 2025
- Finished
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Dec 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.
Who is studied
Potentially eligible participants will be selected from clinical databases of IRCCS Medea.
- Ages
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5 to 17 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Subjects aged between 5 and 17 with typical development. * Subjects aged between 5 and 17 years with neuromotor impairments who are undergoing rehabilitation therapy using the Lokomat and GRAIL devices, according to the existing clinical plan. Exclusion Criteria: * Uncooperative subjects.
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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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Scientific Institute IRCCS E.Medea
Bosisio Parini, LC, 23842, Italy
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