Clinical trial Recruiting at 1 site Observational Ages 12 to 18

Emotional dysregulation in adolescents with complex trauma traits

Official title: Evaluation of Post-traumatic and Neurodevelopmental Symptoms in Adolescents Placed in Child Welfare

Run by University Hospital, Strasbourg, France · NCT07794332 · Data updated 2026-11-12

Researchers will observe teens to see how emotional dysregulation shows up in CPTSD and how it differs from BPD and PTSD.

Quick facts

Study typeObservational
Ages12 Years to 18 Years
SexAll
Enrollment200 (estimated)
SponsorUniversity Hospital, Strasbourg, France
Academic / other
Locations1 site (Strasbourg, Grand Est)
StatusRecruiting
StartedJanuary 30, 2026
Main results expectedSeptember 1, 2027
Study endsMarch 1, 2028
Registry record updatedAugust 31, 2026
Trial IDNCT07794332 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adolescents aged 12–17 who are under ASE Bas-Rhin supervision, fluent in French, affiliated with a social health insurance plan, and whose legal guardian consents to participate.

Probably not a fit

Participants who do not exhibit distinct patterns of emotional dysregulation or who do not meet the specific cPTSD profile may gain limited or no direct benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study will characterize how emotional dysregulation manifests in adolescents aged 12 to 17 with complex post-traumatic presentations. It uses a mixed-methods approach, combining real-life monitoring with in-hospital assessments to understand dynamic emotional processes. The goal is to identify distinguishing features of cPTSD-related dysregulation compared with BPD and PTSD, through measurements taken in daily life and clinical settings. The study is conducted at Strasbourg University Hospital with participants enrolled through ASE Bas-Rhin and is led by the Strasbourg site.

Why it matters

Potential benefit: If successful, the findings could improve understanding of how emotional dysregulation presents in teens with complex trauma and help differentiate cPTSD from BPD and PTSD in clinical assessments.

How similar studies have gone: Prior work in related trauma and emotion regulation research has demonstrated meaningful findings using ecological and clinical assessments, but this exact combination in adolescent cPTSD/BPD/PTSD differentiation is novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adolescent aged 12 to 17
* Entrusted to ASE Bas-Rhin.
* Fluent in French
* Affiliated with a social health insurance scheme
* Agreeing to take part in the study
* Legal representative of the minor or his/her guardian, or his/her representative from the ASE agreeing to take part in the study.

Exclusion Criteria:

* Adolescent refusing to participate in the study
* Legal representative of the minor or his/her guardian, or his/her ASE representative refusing to participate in the study
* Adolescent with severe developmental delay
* Adolescent participating in another research study
* Adolescent deprived of liberty by judicial or administrative decision

Where it's running

  • Hôpitaux Universitaires de Strasbourg
    Strasbourg, Grand Est, France
    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.