Mental Health and Aggression in Congolese Ex-combatants
This study is ongoing, but not recruiting participants.
Sponsor:
University of Konstanz
Collaborator:
German Research Foundation
Information provided by (Responsible Party):
Susanne Schaal, University of Konstanz
ClinicalTrials.gov Identifier:
NCT01625117
First received: January 16, 2012
Last updated: June 20, 2012
Last verified: June 2012
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Purpose
The purpose of this study is examine, whether a treatment approach, which is specifically tailored for perpetrators who have participated in violence (a variant of Narrative Exposure Therapy) is effective in the reduction of instrumental aggression and symptoms of posttraumatic stress disorder.
| Condition | Intervention | Phase |
|---|---|---|
|
Appetitive Aggression Posttraumatic Stress Disorder |
Behavioral: A variant of Narrative Exposure Therapy |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Treatment |
Resource links provided by NLM:
Further study details as provided by University of Konstanz:
Primary Outcome Measures:
- Appetitive aggression (Appetitive Aggression Scale) [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- Symptoms of posttraumatic stress disorder (Posttraumatic Diagnostic Scale, PDS) [ Time Frame: 6 months ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Symptoms of depression (Mini-International Neuropsychiatric Interview) [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- Functionality (Work and Social Adjustment Scale) [ Time Frame: 6 months ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 41 |
| Study Start Date: | May 2011 |
| Estimated Study Completion Date: | September 2012 |
| Primary Completion Date: | May 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| No Intervention: Control Group | |
| Experimental: A variant of Narrative exposure therapy |
Behavioral: A variant of Narrative Exposure Therapy
During the proposed therapy, the client constructs a chronological narrative of his or her whole life which includes all traumatic experiences and perpetrated violent acts. All emotions, cognitions, sensory information, and physiological reactions are activated and linked to the autobiographical context.In five sessions the therapist and the client try to go through all important traumatic experiences and perpetrated violent acts. The sixth session is a group session with four to five clients. The group session is oriented on Interpersonal Psychotherapy and focuses on the role change from soldier to civilian.
|
Detailed Description:
The reintegration of former child soldiers and ex-combatants is a big challenge in war-torn countries. Former child soldiers and ex-combatants often suffer from mental health problems and show enhanced levels of aggression. The present study focuses on the reduction of appetitive aggression and the improvement of mental health in former child soldiers and ex-combatants in DR Congo.
Eligibility| Ages Eligible for Study: | 16 Years to 35 Years |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Ex-combatants in Congo who live in a re-integration camp
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Susanne Schaal, University of Konstanz |
| ClinicalTrials.gov Identifier: | NCT01625117 History of Changes |
| Other Study ID Numbers: | DFG_2011 |
| Study First Received: | January 16, 2012 |
| Last Updated: | June 20, 2012 |
| Health Authority: | Germany: Ethics Commission |
Keywords provided by University of Konstanz:
|
Treatment of ex-combatants Narrative Exposure Therapy for ex-combatants Appetitive Aggression Posttraumatic Stress Disorder |
Additional relevant MeSH terms:
|
Aggression Stress Disorders, Post-Traumatic Stress Disorders, Traumatic |
Behavioral Symptoms Anxiety Disorders Mental Disorders |
ClinicalTrials.gov processed this record on May 19, 2013