Post-Traumatic Stress Disorder (PTSD) Clinical Trials

Find Post-Traumatic Stress Disorder (PTSD) Clinical Trials Near You

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

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

This study aims to characterize emotional dysregulation in complex post-traumatic stress disorder (cPTSD) and to determine the extent to which it can promote the distinction with borderline personality disorder (BPD) and post-traumatic stress disorder (PTSD). As emotional dysregulation is a dynamic process whose phenomenological manifestations are labile, associated with physiological modifications and modulated by cognitive processing, a multiple methodology associating measurements in a real-life ecological context with measurements performed in the hospital will be preferred. Overall, this study proposes to capture, for the first time, the clinical manifestations associated with cPTSD from the perspective of emotional dysregulation and its underlying processes

Eligibility
Participation Requirements
Sex: All
Minimum Age: 12
Maximum Age: 18
Healthy Volunteers: f
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• 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.

Locations
Other Locations
France
Hôpitaux Universitaires de Strasbourg
RECRUITING
Strasbourg
Contact Information
Primary
Carmen SCHRÖDER
carmen.schroder@chru-strasbourg.fr
0033388115248
Time Frame
Start Date: 2026-01-30
Estimated Completion Date: 2028-03-01
Participants
Target number of participants: 200
Related Therapeutic Areas
Sponsors
Leads: University Hospital, Strasbourg, France

This content was sourced from clinicaltrials.gov