Can sound and touch boost brain training for kids with cerebral palsy?

NCT ID NCT07369193

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This pilot study explores whether adding sound and touch to a standard movement-observation therapy can better activate the brain's mirror neuron system in children with cerebral palsy. Twenty kids with CP and 20 typically developing peers, aged 7-25, will watch videos of actions while their brain activity is measured with EEG. Some sessions include sounds and haptic gloves that provide tactile feedback, while others are just visual. The goal is to see if the multisensory version leads to stronger brain responses, which could eventually improve rehabilitation outcomes.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
multisensory action observation treatment (AOT) with haptic gloves and auditory stimuli
What this could lead to
If it works, this could point toward a more effective rehabilitation technique for children with cerebral palsy by enhancing brain activation through multiple senses.
What could go wrong
This is a small, early pilot study with only 40 participants, so results may not apply widely. It measures brain activity, not long-term functional improvement, so real-world benefits remain 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.

Participants

About 40 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2026

Expected to finish

Jun 2027

An estimate. End dates often move.

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.

Who is studied

For this study, 20 children, adolescents, and young adults with typical development will be recruited (community sample), toghether with 20 children and adolescents diagnosed with CP (recruit at the IRCCS Fondazione Stella Maris).

Ages

7 to 25 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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.

Study Group: Inclusion Criteria: * Confirmed diagnosis of cerebral palsy, documented by clinical history and instrumental examinations; * Age between 7 and 25 years at the time of recruitment; * At least one verbal or nonverbal intellectual functioning index \>= 70, to ensure understanding and compliance with the tasks required. Exclusion Criteria: * Severe sensory disorders that compromise the feasibility of the study; * Neuropsychiatric comorbidity that precludes participation in the study. Control group: Inclusion Criteria * Age between 7 and 25 years at the time of recruitment; * Absence of intellectual disability, assessed through age-appropriate versions of the Raven's Progressive Matrices (Coloured Progressive Matrices for children up to 11 years; Standard Progressive Matrices for participants aged 12 years and older), yielding scores within the normative range and used to estimate non-verbal fluid intelligence; * Age-appropriate academic performance with no reports of significant learning difficulties, as verified through parental interview; * Absence of known neurological or psychiatric disorders, confirmed through parental interview; * Absence of motor impairments, defined as scoring above the 25th percentile on the Movement Assessment Battery for Children, Second Edition (MABC-2).

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Action observation are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • IRCCS Fondazione Stella Maris

    RECRUITING

    Calambrone, Pisa, 56128, Italy

More trials for these conditions

Other studies related to the condition(s) this trial covers.