New Identity-Based therapy aims to beat standard CBT for young adults
NCT ID NCT06384196
First seen Jun 26, 2026 · Last updated Sep 17, 2026 · Updated 5 times
Summary
This study tests a new type of talk therapy called Identity-Based Transdiagnostic Therapy (IBTT) for young adults with anxiety or depression. It compares IBTT to a well-known therapy called the Unified Protocol (CBT-based). The goal is to see if IBTT is more engaging and effective at reducing symptoms. The trial will involve 138 participants and uses online tools to explore personal identity.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Identity-Based Transdiagnostic Therapy (IBTT) - a type of talk therapy
- What this could lead to
- If it works, this could offer a more engaging and effective therapy option for young adults struggling with anxiety or depression.
- What could go wrong
- This is a relatively small, early-stage trial (138 participants) comparing a new therapy to an established one. The new therapy may not prove more effective, and results may not apply to everyone.
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 138 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2025
- Expected to finish
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Nov 2027
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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16 to 29 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.
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: • Participants with symptoms of depression and/or anxiety as their primary complaint. Exclusion Criteria: * Participants with post-traumatic stress, bipolar and substance use disorders, psychotic symptoms, organic brain dysfunction, marked suicidal ideation and/or intellectual disability. * Participants receiving psychological treatment, unless it is suspended at the time of inclusion in the study itself in agreement with their therapist. * Participants for whom the use of virtual reality may pose a risk, even a minor risk (epilepsia, acute otorhinolaryngological processes or recent interventions, severe cardiovascular disease, unstable hypertension, and pregnancy). * Participants with substantial visual, hearing, and cognitive deficits. * Participants who do not have enough competence to communicate in Spanish or Catalan.
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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
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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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Associació Centre Higiene Mental Nou Barris
RECRUITINGBarcelona, 08042, Spain
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Badalona Serveis Assistencials
RECRUITINGBadalona, 08911, Spain
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- Can a group program teach teens to cope before therapy starts?