Cognitive training and enhanced treatment for youth at high risk of psychosis in Tunisia
Official title: Cognitive Training vs. Treatment as Usual to Improve Functioning and Reduce Transition Rates in Tunisian CHR Youth: A Feasibility Study
Run by University of California, Los Angeles · NCT06582901 · Data updated 2026-11-12
This study is testing two different treatment approaches to see if they can help young people at high risk for psychosis improve their daily functioning over 12 weeks.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 14 Years to 28 Years |
| Sex | All |
| Enrollment | 54 (estimated) |
| Sponsor | University of California, Los Angeles Academic / other |
| Locations | 1 site (Tunis) |
| Status | Recruiting |
| Started | September 1, 2023 |
| Main results expected | August 31, 2025 |
| Study ends | August 31, 2026 |
| Registry record updated | November 25, 2025 |
| Trial ID | NCT06582901 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are youth who meet the criteria for Clinical High Risk for Psychosis and have sufficient fluency in Arabic, French, or English.
✕Probably not a fit
Patients with known neurological disorders or significant substance use issues may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to improve daily functioning in youth identified as clinically high risk for psychosis through two treatment approaches: a Cognitive Training (CT) program and an Enhanced Treatment as Usual (E-TAU) group. Participants will be randomly assigned to one of the two groups, with treatments lasting 12 weeks and involving both in-clinic and home sessions. The CT program includes engaging cognitive exercises designed to enhance thinking skills, while E-TAU provides standard care with additional group activities. Assessments of clinical symptoms and cognitive functioning will be conducted at baseline, mid-point, and conclusion of the treatment.
Why it matters
Potential benefit: If successful, this study could lead to improved cognitive functioning and daily life skills for youth at high risk of developing psychosis.
How similar studies have gone: Other studies have shown promise in using cognitive training approaches for at-risk populations, suggesting potential for success in this novel application.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Meets Comprehensive Assessment for At Risk Mental States (CAARMS) criteria for Clinical High Risk * If under the age of 18, the subject has a parent or guardian who can sign consent forms * Premorbid Intelligence Quotient not less than 70 * Sufficient fluency in Arabic, French, or English to avoid invalidating research measures * Residence likely within commuting distance of Razi University Hospital Exclusion Criteria: * Evidence of known neurological disorder, e.g. epilepsy or significant head injury that could account for the CHR symptoms * Evidence of significant and habitual alcohol or substance use in the 6 months prior to study entry * Evidence that the clinical high-risk symptoms were substance-induced
Where it's running
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Razi University Hospital
Tunis, Tunisia Recruiting
Study contacts
- Principal investigator: Joseph Ventura, Ph.D. — UCLA Department of Psychiatry & Biobehavioral Sciences
- Study coordinator: Joseph Ventura, Ph.D.
- Email: jventura@mednet.ucla.edu
- Phone: 310-245-2811
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Accelerated Brain Stimulation for Young People at Risk of Psychosis
This study tests a five-day accelerated brain-stimulation treatment to see if it is safe and tolerable for young people at risk for psychosis and to explore biomarkers that might show whether it works.
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Recovery-oriented suicide prevention for young people at clinical high risk for psychosis
This program tests a peer-supported, clinician-led suicide prevention group for young people at clinical high risk for psychosis to see if it helps reduce suicidal thoughts and support recovery.
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Mindfulness group experiences for young people at high risk for or early in psychosis
This project tries to understand how group mindfulness sessions feel for French-speaking young people aged 15–30 who are at ultra‑high risk for psychosis or have had a first episode.
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Biomarker changes after MT1988 dosing in young people at high risk for psychosis
This will test whether two doses of MT1988 taken twice daily for 8 weeks change biomarker tests in 17–30-year-olds at high risk for psychosis compared with placebo.
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Digital DBT for Youth at Risk of Psychosis
This study tests a self-guided digital DBT program to help young people aged 14–35 who are at clinical high risk for psychosis, comparing it to usual care over eight weeks.
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French version of the Schizophrenia Proneness Instrument for children and adolescents (SPI-CY)
This project will test the French SPI-CY to see if it reliably identifies French-speaking adolescents (ages 12–17) who are at high risk for developing psychosis.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.