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Clinical Trials/DRKS00034621
DRKS00034621
Not Yet Recruiting
N/A

Transdiagnostic study of Adverse Childhood Experiences in people with mental health problems - TrACE

MU Klinikum, Klinik für Psychiatrie und Psychotherapie0 sites550 target enrollmentJuly 10, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
DSM-5: 300.4 Persistent depressive disordersICD-11: 6B41 Complex post-traumatic stress disorder
Sponsor
MU Klinikum, Klinik für Psychiatrie und Psychotherapie
Enrollment
550
Status
Not Yet Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 10, 2024
End Date
TBD
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
MU Klinikum, Klinik für Psychiatrie und Psychotherapie

Eligibility Criteria

Inclusion Criteria

  • We will include participants with sufficient German language skills to perform all questionnaires, interviews and introductions of the behavioral paradigm. Patients have to meet diagnostic criteria of one of the following main diagnoses according to the DSM\-5: Diagnosis of a BPD (301\.83\), PDD (300\.4, 296\.2x, 296\.3x, 296\.3x), cPTSD (309\.9\), ED (296\.xx) or SSD (300\.82\). Healthy controls have to not fulfill a psychiatric disorder assessed within a screening.

Exclusion Criteria

  • Clinical participants will be excluded if fulfilling DSM\-5 criteria of an active substance\-dependency (abstinence shorter than 6 months), a psychotic disorder or a bipolar I or II disorder or acute suicidality (as main or comorbid diagnosis). Participants will be screened and diagnosed by a trained clinician based on the DSM\-5 criteria (SCID\-5\-CV and SCID\-5\-PD interview). All Individuals will be excluded if having a current or past somatic or neurological disorders with effects on the brain or if currently pregnant. Non\-clinical participants will be excluded when having a history of a psychiatric disorder or a psychotherapeutic/psychopharmacological intervention within the last 10 years (reviewed by telephone screening and psychometric assessments). Participants with a regular (daily) current intake of benzodiazepines will be excluded due to confounding aspects for the experimental cyberball paradigm and the psychometric questionnaires.

Outcomes

Primary Outcomes

Not specified

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