ClinicalTrials.gg
Status unknownNCT01624987Updated Jul 30, 2013

Intervention to Support the Reintegration of Former Combatants and Soldiers

A Phase 2/3 interventional study of NET for Forensic Offender Rehabilitation (FORNET): a variant of Narrative Exposure Therapy and Control group in Appetitive Aggression and Post-traumatic Stress Disorder, sponsored by University of Konstanz. Status unknown at 1 site in Congo. Open to male participants aged 16 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2013-07-30.

Sponsored by University of Konstanz · Phase 2/3, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jul 2013), so the status shown — last known as Enrolling by invitation — may be out of date.
Phase
Phase 2/3
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
16 Years to 70 Years
Sex
Male
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 28 studies in Stress Disorders, Post-Traumatic by University of Konstanz — none open to participants now, none under way, none of them phase 3. Stress Disorders, Post-Traumatic · University of Konstanz.

Planned enrollment
8th of 28
100 · median 48
Started
2012
with 2 others
Phase 2/3
Only one
of the 28
Registered
14th of 28
by date

Among the 28 studies in Stress Disorders, Post-Traumatic by University of Konstanz, this one is the 8th largest by planned enrollment, is one of 3 that started in 2012, is the only one in phase 2/3, and was the 14th registered.

By phase

28 studies; the count open now beside each. This study's row is marked.

No phase18 · 0 open
Phase 24 · 0 open
Phase 34 · 0 open
Phase 11 · 0 open
Phase 2/3this study1 · 0 open

By the year they started

First in 2003; this study’s year is marked. 3 started in 2012.

Size and results

Median enrollment 48 across the 28 interventional studies. Of the 25 that completed or were terminated, 0 (0%) have results posted.

Download CSVWith an account: the 28 studies in Stress Disorders, Post-Traumatic by University of Konstanz as a file.
02

Study 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.

Read the 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.

03

Conditions studied

  • Appetitive Aggression
  • Post-traumatic Stress Disorder

Keywords

  • Treatment of ex-combatants
  • FORNET for ex-combatants
  • Appetitive Aggression
  • Post-traumatic Stress Disorder
04

Who can participate

Ages eligible
16 Years to 70 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

05

Study design

Phase
Phase 2 / Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    NET for Forensic Offender Rehabilitation

    Narrative Exposure Therapy for Forensic Offender Rehabilitation (FORNET)

    Behavioral: NET for Forensic Offender Rehabilitation (FORNET): a variant of Narrative Exposure Therapy · Other: Control group

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.

06

What researchers measure

Primary outcomes

  1. Appetitive Aggression (Appetitive Aggression Scale)

    Time frame: 6 months

  2. Symptoms of post-traumatic stress disorder (Post-traumatic Diagnostic Scale, PDS)

    Time frame: 6 months

Secondary outcomes

  1. Symptoms of depression (Patient Health Questionnaire (PHQ-9)

    Time frame: 6 months

  2. Functionality (Work and Social Adjustment Scale)

    Time frame: 6 months

  3. Substance abuse

    Time frame: 6 months

  4. Re-integration questionnaire

    Time frame: 6 months

07

Study locations

1 site
  • Transit Camp for ex-combatants/Reintegration camp for ex-combatants (ETN)
    Goma, Congo
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 30, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01624987
Lead sponsor
University of Konstanz
Collaborators
World Bank
Responsible party
Susanne Schaal (Susanne Schaal, University of Konstanz) — Principal investigator
First posted
Jun 21, 2012
Start date
Jun 2012
Primary completion
Feb 2014 (estimated)
Completion
Feb 2014 (estimated)
Last update
Jul 30, 2013

Study contacts

Thomas Elbert, Prof. Dr.
study director · University of Konstanz

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2013. You cannot join it, but the record below documents what was studied.

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