New therapy aims to heal emotional scars after childhood brain injury
NCT ID NCT07303075
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a family-centred talking therapy (ACT) for young people aged 11-18 with acquired brain injury and their parents. Up to 6 families will receive 12 online therapy sessions. The goal is to see if the therapy is feasible and can improve emotional wellbeing, psychological flexibility, and participation in daily life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Acceptance and Commitment Therapy (ACT) - a type of talk therapy that helps people cope with difficult thoughts and feelings
- What this could lead to
- If this therapy works, it could offer a new way to help young brain injury survivors and their families manage emotional challenges and improve quality of life.
- What could go wrong
- This is a very small, early feasibility study with only 6 families, so results may not apply to everyone. The therapy is delivered online, which may not suit all families.
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 6 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2025
An estimate. Start dates often move.
- Expected to finish
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Jun 2026
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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11 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 Both the CYP-ABI and parent participants must meet the inclusion criteria to be recruited to the study. CYP-ABI participant inclusion criteria include: * Aged 11 to 18 years at time of recruitment. * Living at home with parent/guardian. * Received treatment for an ABI. * Have sufficient cognitive ability to engage with therapy sessions. * Has capacity to provide verbal or written informed consent (aged 16 and above) or assent (aged 15 and younger). * Has the ability to speak sufficient English to understand and engage with the therapeutic and research materials * Consents for parent/guardian participant involvement in study. Parent participant inclusion criteria include: * Aged \> 18 at time of recruitment. There is no upper age limit. * Has the ability to speak sufficient English to understand and engage with the therapeutic and research materials * Has capacity to provide verbal or written informed consent for self and CYP participant. Exclusion Criteria: CYP-ABI and parent participant exclusion criteria include: • CYP or parent participants are currently accessing or have accessed structured psychological intervention within 6 months of study recruitment.
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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 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.
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Other studies related to the condition(s) this trial covers.
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