Prevention of Post-Traumatic Stress Disorder in Soldiers

Sponsor
University of Konstanz (Other)
Overall Status
Completed
CT.gov ID
NCT01729325
Collaborator
The Volkswagen Foundation (Other)
118
1
2
28.9
4.1

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Preventive Narrative Exposure Therapy
Phase 2

Study Design

Study Type:
Interventional
Actual Enrollment :
118 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Prevention of Post-Traumatic Stress Disorder in Relation to Appetitive Aggression in Burundian Soldiers Deployed in a Peace-keeping Mission in Somalia
Study Start Date :
Nov 1, 2012
Actual Primary Completion Date :
Jan 1, 2013
Actual Study Completion Date :
Apr 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Preventive Narrative Exposure Therapy

Treatment with Pre-NET before deployment in peace-keeping mission

Behavioral: Preventive 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.

No Intervention: No treatment control

Outcome Measures

Primary Outcome Measures

  1. Severity of traumatic symptoms measured via the Post-traumatic Stress Disorder Scale-Interview (PSS-I) [15 months]

  2. Extend of appetitive aggression via the Appetitive Aggressions Scale (AAS) [15 months]

Secondary Outcome Measures

  1. Severity of depressive symptoms measured via the Patient Health Questionnaire-9 (PHQ-9) [15 months]

  2. Strength of suicidal ideation measured via the MINI [15 months]

  3. Physical health complains [15 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 60 Years
Sexes Eligible for Study:
Male
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Burundian Army (FDN) Bujumbura Burundi

Sponsors and Collaborators

  • University of Konstanz
  • The Volkswagen Foundation

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Anselm Crombach, Dipl.-Psych., University of Konstanz
ClinicalTrials.gov Identifier:
NCT01729325
Other Study ID Numbers:
  • UKULBUSO2012
First Posted:
Nov 20, 2012
Last Update Posted:
Jun 4, 2015
Last Verified:
Jun 1, 2015

Study Results

No Results Posted as of Jun 4, 2015