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Adressing PTSD Symptoms and Aggressive Behavior in Vulnerable Children in Burundi

Treating Posttraumatic Stress Disorder and Reducing Aggressive Behavior in Street Children and Vulnerable Children in Burundi Using Narrative Exposure Therapy for Forensic Offender Rehabilitation.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03498482
Enrollment
19
Registered
2018-04-13
Start date
2017-03-15
Completion date
2018-01-31
Last updated
2018-04-13

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

Conditions

Aggressive Behavior, Posttraumatic Stress Disorder

Brief 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.

Interventions

BEHAVIORALNarrative 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.

Sponsors

Vivo international e.V.
CollaboratorINDUSTRY
Psychologues sans Frontières Burundi
CollaboratorOTHER
Université Lumière de Bujumbura
CollaboratorOTHER
University of Konstanz
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 20 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* Psychotic symptoms

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
Change of number of aggressive acts measured via an adaption of the Domestic and Community Violence Checklistbaseline; 5 months follow-up; 9 months follow-up
Change of experienced shame measured via the Shame Variability Questionnairebaseline; 5 months follow-up; 9 months follow-up

Countries

Burundi

Outcome results

None listed

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