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Clinical Trials/NCT01729325
NCT01729325
Completed
Phase 2

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

University of Konstanz1 site in 1 country118 target enrollmentNovember 2012

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Post-traumatic Stress Disorder (PTSD)
Sponsor
University of Konstanz
Enrollment
118
Locations
1
Primary Endpoint
Severity of traumatic symptoms measured via the Post-traumatic Stress Disorder Scale-Interview (PSS-I)
Status
Completed
Last Updated
10 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
November 2012
End Date
April 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Sponsor
University of Konstanz
Responsible Party
Principal Investigator
Principal Investigator

Anselm Crombach

Dipl.-Psych.

University of Konstanz

Eligibility Criteria

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

Outcomes

Primary Outcomes

Severity of traumatic symptoms measured via the Post-traumatic Stress Disorder Scale-Interview (PSS-I)

Time Frame: 15 months

Extend of appetitive aggression via the Appetitive Aggressions Scale (AAS)

Time Frame: 15 months

Secondary Outcomes

  • Physical health complains(15 months)
  • Severity of depressive symptoms measured via the Patient Health Questionnaire-9 (PHQ-9)(15 months)
  • Strength of suicidal ideation measured via the MINI(15 months)

Study Sites (1)

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