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Intervention to Support the Reintegration of Former Combatants and Soldiers

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01624987
Enrollment
100
Registered
2012-06-21
Start date
2012-06-30
Completion date
2014-02-28
Last updated
2013-07-30

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

Conditions

Appetitive Aggression, Post-traumatic Stress Disorder

Keywords

Treatment of ex-combatants, FORNET for ex-combatants, Appetitive Aggression, Post-traumatic Stress Disorder

Brief summary

The project aims to investigate if trauma-related disorders and appetitive aggression can be reduced in former ex-combatants in DR Congo when a specific intervention (Narrative Exposure Therapy for Forensic Offender Rehabilitation, FORNET) is delivered by trained local personnel (phase 1). In a second step, the project aims to investigates the treatment success if this specific therapy is carried out by local personnel who have been trained by other local personnel (train the trainer, phase 2) under the supervision of experts of the University of Konstanz.

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. The project consists of four steps: 1. Training of selected DDRRR personnel(first generation)in FORNET (a variant of Narrative Exposure Therapy to treat trauma-related disorders and to reduce appetitive aggression)by experts from the University of Konstanz. 2. Treatment phase 1: Intervention will be carried out by therapists of the first generation. The trained therapists of the first generation will be supervised from the experts of the University of Konstanz. 3. Training of a second generation of DDRRR personnel in FORNET by the therapists of the first generation. 4. Treatment phase 2: Intervention will be carried out by therapists of the second generation. The trained therapists of the second generation will be supervised from the therapists of the first generation. The study is conceived as a randomized controlled study. In phase 1 and in phase 2, study participants will be randomized allocated to the intervention group (FORNET) and the control group (no intervention). The treatment effect will be measured by pre-post and 6-months follow-up evaluations.

Interventions

BEHAVIORALNET for Forensic Offender Rehabilitation (FORNET): 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 trained 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.

OTHERControl group

The control group receives no intervention.

Sponsors

World Bank
CollaboratorOTHER
University of Konstanz
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
16 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Ex-combatants who live in a transit camp in Goma, Congo.

Design outcomes

Primary

MeasureTime frame
Appetitive Aggression (Appetitive Aggression Scale)6 months
Symptoms of post-traumatic stress disorder (Post-traumatic Diagnostic Scale, PDS)6 months

Secondary

MeasureTime frame
Symptoms of depression (Patient Health Questionnaire (PHQ-9)6 months
Functionality (Work and Social Adjustment Scale)6 months
Substance abuse6 months
Re-integration questionnaire6 months

Countries

Republic of the Congo

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026