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Video game rehab at home: a new way to heal the brain after injury?

NCT ID NCT07733336

Disease control Sponsor: Fondazione Don Carlo Gnocchi ETS Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 29, 2026 · Last updated Aug 12, 2026 · Updated 3 times

Summary

This pilot trial compares a home-based cognitive-motor telerehabilitation program using exergames to standard outpatient rehabilitation for people recovering from traumatic brain injury. Participants will complete 20 sessions over 7 weeks, and researchers will measure changes in functional independence, thinking skills, mobility, and quality of life. The goal is to see whether a home-based approach can match or outperform traditional clinic-based rehab.

What this could mean

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

Active substance
home-based cognitive-motor telerehabilitation (exergame) program
What this could lead to
If effective, this approach could offer a convenient, home-based alternative to standard outpatient rehab for people recovering from traumatic brain injury.
What could go wrong
This is a small pilot study with only 30 participants, so results may not apply broadly. The home-based program may be less effective than in-person therapy for some individuals.

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

About 30 people

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

Expected to start

Nov 2026

An estimate. Start dates often move.

Expected to finish

Mar 2029

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.

Ages

18 to 75 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.

TBI patients Inclusion Criteria * Discharge from intensive inpatient post-acute rehabilitation following a first traumatic brain injury (TBI). * Level of Cognitive Functioning Scale (LCF) score ≥ 6, indicating appropriate and goal-directed cognitive responses. * Ability to walk at least 30 meters, with or without an assistive device. * Ability to maintain an unsupported standing position for at least 3 minutes. * Provision of written informed consent. TBI patients Exclusion Criteria * Diagnosis or suspected diagnosis of a neurodegenerative disorder. * Previous history of traumatic brain injury. * History of major psychiatric disorders (e.g., schizophrenia or bipolar disorder), primary sleep disorders, or epilepsy. * Severe visual or auditory impairment that could interfere with study assessments or participation in the rehabilitation program. * Severe expressive and/or receptive aphasia. * Language barriers preventing reliable cognitive assessment or informed consent procedures. * Current pregnancy. Healthy Subjects - Exclusion Criteria * Presence of any neurological, sensrory, cognitive, psychiatric, cardiopulmonary, or musculoskeletal condition that may affect study participation or outcome measures * Language barriers preventing reliable cognitive assessment or informed consent procedures. * Current pregnancy.

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Conditions

The condition(s) this trial relates to.

Brain Injuries, Traumatic traumatic brain injury

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Traumatic brain injury

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. 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 Don Carlo Gnocchi ETS

    Milan, Italy, 20148, Italy

  • Istituto Auxologico Italiano IRCCS

    Milan, Italy, 20122, Italy

More trials for these conditions

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