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Prevention of Post-Traumatic Stress Disorder in Soldiers

Prevention of Post-Traumatic Stress Disorder in Relation to Appetitive Aggression in Burundian Soldiers Deployed in a Peace-keeping Mission in Somalia

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01729325
Enrollment
118
Registered
2012-11-20
Start date
2012-11-30
Completion date
2015-04-30
Last updated
2015-06-04

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

Conditions

Aggressive Behavior, Post-traumatic Stress Disorder (PTSD)

Keywords

Post-traumatic Stress disorder (PTSD), Aggressive Behavior, Appetitive Aggression, Resilience, Preventive Narrative Exposure Therapy

Brief summary

Soldiers in conflict or former conflict regions deployed in peace-keeping missions were and are often exposed to multiple traumatic events and situations in which they are forced to engage in violent behavior. The Preventive Narrative Exposure Therapy (Pre-NET) aims to reinforce resilience thereby reducing the risk of developing or aggravating PTSD or other mental disorders as a result of traumatic experiences. The effective prevention of mental disorders as a result of war deployment is expected to facilitate reintegration in civil life after deployment and reduce uncontrolled violence.

Interventions

BEHAVIORALPreventive Narrative Exposure Therapy

During Pre-NET the client, with the assistance of the therapist, constructs a chronological narrative of his whole life with a focus on exposure to traumatic stress. Empathic understanding, active listening, congruency and unconditional positive regard are key components of the therapist's behavior who asks in detail for emotions, cognitions, sensory information, and physiological reactions, linking them to an autobiographical context. During two sessions a chronological overview of the whole life with a focus on traumatic events is developed and the most important traumatic experiences are processed.

Sponsors

The Volkswagen Foundation
CollaboratorOTHER
University of Konstanz
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
MALE
Age
20 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Exposure to traumatic experiences derived from expert interviews with scores of the Traumatic Life Event List for War and Torture * Soldiers are part of the Burundian army and of the joint African Union and United Nations peacekeeping mission in Somalia (AMISOM)

Exclusion criteria

* Current use of mind altering drugs * Psychotic symptoms

Design outcomes

Primary

MeasureTime frame
Severity of traumatic symptoms measured via the Post-traumatic Stress Disorder Scale-Interview (PSS-I)15 months
Extend of appetitive aggression via the Appetitive Aggressions Scale (AAS)15 months

Secondary

MeasureTime frame
Severity of depressive symptoms measured via the Patient Health Questionnaire-9 (PHQ-9)15 months
Strength of suicidal ideation measured via the MINI15 months
Physical health complains15 months

Countries

Burundi

Outcome results

None listed

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