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Cognitive-behavioral treatment for female patients with PTSD and SUD

Cognitive-behavioral treatment for female patients with PTSD and SUD - CANSAS 2.A

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00004288
Enrollment
342
Registered
2012-09-18
Start date
2012-10-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

substance abuse F43.1

Interventions

Group 1: "Seeking safety"-branch: psychological intervention programm comprising 14 group sessions (90 minutes each) for approx. 8 participants and an additional individual introduction and closing se

Sponsors

Klinik für Psychiatrie und Psychotherapie, Universitätsklinikum Hamburg-Eppendorf
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: diagnosis of substance abuse disorder (according to DSM-IV), at least partial PTSD (according to DSM-IV), sufficient knowledge of the German language

Exclusion criteria

Exclusion criteria: intravenous drug use, acute psychosis, organic mental disorder, severe cognitive impairment, suicidal tendency, characteristics interfereing with therapy (e.g. impending incarceration, life-threatening, instable medical illness)

Design outcomes

Primary

MeasureTime frame
PTSD symptoms Method: interview: SCID-I, PSS-I, self-report questionnaire: PDS, time points: T0: before therapy, T1: after therapy (16 weeks later), T2: 3 months after the end of therapy, T3: 6 months after the end of theray

Secondary

MeasureTime frame
substance use mehtod: interview: ASI-Lite, SCID-I), emotion regulation method: self-report questionnaire: H-FERST, DERS time points: T0: before therapy, T1: after therapy (16 weeks later), T2: 3 months after the end of therapy, T3: 6 months after the end of theray

Countries

Germany

Contacts

Public ContactIngo Schäfer

Kklinik für Psychiatrie und Psychotherapie, Universitätsklinikum Hamburg-Eppendorf

ischaefer@uke.de040-7410 59290

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026