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Clinical Trials/NCT02259530
NCT02259530
Completed
Not Applicable

Sustainable and Adapted Treatment Strategies to Restore Psychological Functioning and Mental Health Among Displaced Somalis: Preparation of a Multicenter Treatment Study (P114/02/2014): Pilot Study 3.

University of Konstanz1 site in 1 country20 target enrollmentJanuary 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Posttraumatic Stress Disorder
Sponsor
University of Konstanz
Enrollment
20
Locations
1
Primary Endpoint
Posttraumatic Stress Diagnostic Scale (PDS)
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The research project will offer psychotherapeutic treatment to Somali refugees with PTSD and comorbid khat dependence. In this case series, evidence-based techniques will be applied and adapted to the cultural background of Somali refugees in Kenya.

Detailed Description

More than 500.000 Somali refugees live in Kenya. This group is especially burdened by high rates of exposure to traumatic events, high prevalence of PTSD and a high comorbidity with substance use disorders, mainly related to khat (catha edulis). There's a shortage of literature on psychotherapeutic methods that are applicable in this group. The aim of this case series is to develop modifications of standard therapeutic techniques to the Somali culture and to the needs of this group. Twenty successive cases will be recruited from a community clinic where refugees often seek for treatment because of psychiatric problems. Senior level psychotherapists will apply and adapt techniques and approaches like Community Reinforcement Approach (CRA), Relapse Prevention (RP), and Narrative Exposure Therapy (NET); all sessions will be video recorded. Regular supervision with external experts and group discussions will be held to evaluate and adapt the single procedures and techniques. The aim of this study is the development of a standardized approach that can be used in a Randomized Controlled Trial which will be conduced in the future.

Registry
clinicaltrials.gov
Start Date
January 2015
End Date
December 2015
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Sponsor
University of Konstanz
Responsible Party
Principal Investigator
Principal Investigator

Michael Odenwald

Researcher

University of Konstanz

Eligibility Criteria

Inclusion Criteria

  • PTSD (DSM-IV) Khat Dependence (DSM-IV)

Exclusion Criteria

  • Severe Psychotic Disorder Suicidality Mental Disability

Outcomes

Primary Outcomes

Posttraumatic Stress Diagnostic Scale (PDS)

Time Frame: 3 months

Pre-post change of self-reported PTSD-symptom severity

Time-Line Follow Back(TLFB)

Time Frame: 3 months

Pre-post change of self-reported days with khat use

Secondary Outcomes

  • Hopkins Symptom Checklist (HSCL)(3 months)

Study Sites (1)

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