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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03498482
Other study ID # UKCR17
Secondary ID
Status Completed
Phase N/A
First received December 22, 2017
Last updated April 12, 2018
Start date March 15, 2017
Est. completion date January 31, 2018

Study information

Verified date April 2018
Source University of Konstanz
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Children either living in the streets of Bujumbara or that are similarly affected by extreme poverty or violence are regularly exposed to traumatic events. Additionally, they often find themselves in situations where engaging in violent behavior appears to be useful or even necessary for survival. The Narrative Exposure Therapy for violent offenders (FORNET) aims to reduce both PTSD symptoms and aggressive behavior. It helps the children to anchor fearful experiences and potential positive emotions linked to violent behaviour in the past. Additionally, visions for the future are developed in order to enable reintegration into the family.

The investigators want to provide evidence, that FORNET effectively reduces PTSD symptoms and ongoing aggressive behavior which in change facilitates reintegration into society.


Recruitment information / eligibility

Status Completed
Enrollment 19
Est. completion date January 31, 2018
Est. primary completion date January 31, 2018
Accepts healthy volunteers No
Gender All
Age group 8 Years to 20 Years
Eligibility Inclusion Criteria:

- High degree of symptoms of posttraumatic stress disorder according to UCLA PTSD Reaction Index

Exclusion Criteria:

- Psychotic symptoms

Study Design


Intervention

Behavioral:
Narrative Exposure Therapy for Forensic Offender Rehabilitation (FORNET)
FORNET aims to reduce trauma-related symptoms and aggressive behavior via narrative exposure of traumatic and violent life events.

Locations

Country Name City State
Burundi vivo international & Psychologues sans Frontières mental health center Bujumbura Bujumbura Mairie

Sponsors (4)

Lead Sponsor Collaborator
University of Konstanz Psychologues sans Frontières Burundi, Université Lumière de Bujumbura, Vivo international e.V.

Country where clinical trial is conducted

Burundi, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of load of traumatic symptoms measured via the UCLA Adolescent PTSD Index (PTSD scale administered by Clinicians) baseline; 5 months follow-up; 9 months follow-up
Secondary Change of number of aggressive acts measured via an adaption of the Domestic and Community Violence Checklist baseline; 5 months follow-up; 9 months follow-up
Secondary Change of experienced shame measured via the Shame Variability Questionnaire baseline; 5 months follow-up; 9 months follow-up
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