Clinical trial Recruiting at 1 site Interventional Ages 15 to 18

Trauma-Focused Therapy for Refugee Minors with PTSD in Greece

Official title: Implementation, Cultural Adaptation, and Efficacy Evaluation of Trauma-Focused Cognitive Behavioral Therapy (TF-CBT) for Unaccompanied Refugee Minors in Greece

Run by Panteion University · NCT06975280 · Data updated 2026-11-12

This study is testing if a special therapy for trauma can help unaccompanied refugee teens in Greece with PTSD feel better compared to the usual treatment they receive.

Quick facts

Study typeInterventional
Ages15 Years to 18 Years
SexAll
Enrollment60 (estimated)
SponsorPanteion University
Academic / other
Locations1 site (Athens)
StatusRecruiting
StartedApril 13, 2023
Main results expectedDecember 2025
Study endsFebruary 2026
Registry record updatedMay 16, 2025
Trial IDNCT06975280 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are unaccompanied minors aged 15-18 residing in accommodation centers or Supported Independent Living programs in Greece with a diagnosis of PTSD.

Probably not a fit

Patients with intellectual disabilities, acute suicidality, or significant comorbid psychiatric disorders 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 randomized controlled trial evaluates the effectiveness of Trauma-Focused Cognitive Behavioral Therapy (TF-CBT) compared to Treatment-as-Usual (TAU) for unaccompanied refugee minors aged 15-18 in Greece who are experiencing PTSD. Participants will be randomly assigned to either the TF-CBT intervention group or the TAU control group, with assessments conducted at baseline, post-intervention, and three months later using standardized psychometric tools. The study aims to adapt TF-CBT to the Greek cultural context and provide guidelines for its implementation, addressing the urgent need for effective mental health interventions for this vulnerable population.

Why it matters

Potential benefit: If successful, this study could significantly reduce PTSD symptoms and improve overall mental health for unaccompanied refugee minors.

How similar studies have gone: While TF-CBT has been effective in other populations, this is the first randomized controlled trial assessing its efficacy specifically for unaccompanied refugee minors in Greece.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Be unaccompanied upon arrival in Greece and aged between 15-18 years old.
* Being diagnosed with PTSD based on DSM-5 criteria. Young refugees with post-traumatic stress symptoms (PTSS), as delineated by high or moderate trauma-related distress in the Child and Adolescent Trauma Screen (CATS), will also be eligible to participate in the study.
* Reside in an accommodation center or SIL program for UAMs in Greece.
* Have a stable living arrangement for at least 2-3 weeks prior to the intervention.
* Not be expected to relocate within the 2-3 months following the start of the intervention.

Exclusion Criteria:

* a diagnosed intellectual disability (IQ \< 70) or another developmental disorder
* acute suicidality or life-threatening self-harm behavior
* significant risk of harm to others
* comorbidity with bipolar disorder or a psychotic disorder
* substance abuse.

Where it's running

  • General Secretariat for Vulnerable Persons and Institutional Protection, Ministry of Migration and Asylum
    Athens, Greece
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.