Skip to content

Treatment of Posttraumatic Stress Disorder and Aggressive Behavior in Soldiers and Ex-combatants

Formation, Orientation and Rehabilitation by Means of Narrative Exposure Therapy (FORNET) for Returning Soldiers of the African Union Mission to Somalia, Male and Female Ex-combatants in Burundi

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02242136
Enrollment
56
Registered
2014-09-16
Start date
2014-09-30
Completion date
2015-10-31
Last updated
2017-11-29

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

Conditions

Aggressive Behavior, Appetitive Aggression, Posttraumatic Stress Disorder

Keywords

Posttraumatic Stress Disorder, Aggressive Behavior, Appetitive Aggression, Treatment, FORNET

Brief summary

Soldiers deployed in peace-keeping missions as well as ex-combatants in conflict or former conflict regions were and are often exposed to multiple traumatic events and situations in which they are forced to engage in violent behavior. The treatment program Formation, Orientation and Rehabilitation by means of Narrative Exposure Therapy (FORNET) is a short-term, culturally sensitive treatment approach that aims to reduce Posttraumatic Stress Disorder (PTSD) symptoms as well as the risk to engage in uncontrolled violent behavior. Addressing trauma-related mental disorders as well as emotions related to aggression by means of FORNET is expected to facilitate reintegration in civil life and reduce uncontrolled violence. The investigators want to provide evidence, that FORNET is an effective and efficient module to assist soldiers after deployment in Somalia and/or male and female ex-combatants who fought in the civil war in Burundi. In addition the investigators aim to explore how traumatic incidences and maltreatment during childhood may influence treatment outcomes.

Interventions

BEHAVIORALFORNET

Sponsors

Université Lumière de Bujumbura
CollaboratorOTHER
The Volkswagen Foundation
CollaboratorOTHER
University of Konstanz
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* High degree of symptoms of posttraumatic stress disorder according to the Posttraumatic Symptom Scale, * High degree of appetitive aggression, * Violent behavior during the past three months

Exclusion criteria

* Current use of mind altering drugs, * Psychotic symptoms

Design outcomes

Primary

MeasureTime frame
Change in Diagnosis and load of PTSD symptoms assessed via the Posttraumatic Symptom Scale - Interview (PSS-I)baseline, two follow-up assessments are planned within the period of 3 to 12 months post-treatment. Exact time of follow-up will be varied systematically within this period.
Change from baseline in the extend of appetitive aggression assessed via the Appetitive Aggression Scale (AAS)baseline, two follow-up assessments are planned within the period of 3 to 12 months post-treatment. Exact time of follow-up will be varied systematically within this period.
Change in number of committed violent acts during the past three months assessed via the Domestic and Community Violence Checklist (DCVC)baseline, two follow-up assessments are planned within the period of 3 to 12 months post-treatment. Exact time of follow-up will be varied systematically within this period.

Secondary

MeasureTime frame
Change from baseline in load of depressive symptoms assessed via the Patient Health Questionnaire-9 (PHQ-9)baseline, two follow-up assessments are planned within the period of 3 to 12 months post-treatment. Exact time of follow-up will be varied systematically within this period.
Change in strength of suicidal ideation measured via the Mini International Neuropsychiatric Interview (M.I.N.I.)baseline, two follow-up assessments are planned within the period of 3 to 12 months post-treatment. Exact time of follow-up will be varied systematically within this period.
Change in physical health complainsbaseline, two follow-up assessments are planned within the period of 3 to 12 months post-treatment. Exact time of follow-up will be varied systematically within this period.

Countries

Burundi

Outcome results

None listed

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