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Treatment of Formerly Abducted Children (FAC) in Uganda

A Randomized Controlled Clinical Trial (RCCT) to Test the Effectiveness of Narrative Exposure Therapy (NET) Versus an Attention Control Condition (AC) in Reducing Trauma Related Symptoms in Formerly Abducted Children and Former Child Soldiers Suffering From Posttraumatic Stress Disorder (PTSD)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00552006
Enrollment
85
Registered
2007-11-01
Start date
2007-11-30
Completion date
2009-11-30
Last updated
2011-03-08

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

Conditions

Stress Disorders, Post-Traumatic

Keywords

PTSD, Treatment, Randomized Controlled Clinical Trial, Combat, Child Soldiers, Dissemination, Narrative Exposure Therapy, Africa

Brief summary

In the aftermath of traumatic experiences like natural disasters or man-caused traumatic events, such as war experiences, a substantial part of the affected individuals develop a number of psychological symptoms. The characteristic symptom pattern occurring in the aftermath of traumatic events is called posttraumatic stress disorder (PTSD) and includes functional impairment of the affected individuals. The investigators want to test whether Narrative Exposure Therapy (NET) is an effective tool in reducing trauma related symptoms in formerly abducted children and youths and former child soldiers, when applied by lay personnel.

Interventions

BEHAVIORALNarrative Exposure Therapy

Narrative Exposure Therapy (NET) is based on Testimony Therapy in combination with cognitive behavioural exposure techniques and elements of client-centered counselling. In cooperation with the therapist the clients can restore their autobiographic memories about their traumatic experiences. In this way fragmentary memories are transformed into a coherent narrative structure. This practice enables the processing of painful emotions and the construction of clear contingencies of dangerous and safe conditions, generally leading to significant emotional recovery. Therapeutic aims are the reduction of PTSD-Symptomload via activation of fear-network and habituation of fear and the placement of traumatic experiences in a reconstructed, detailed and consistent autobiography. NET will be applied in eight sessions (90-120min/session) in a standardized, manualized manner.

BEHAVIORALAcademic Counseling

Missing time in educational life is one major issue for formerly abducted people. The Academic Counseling (AC) intervention is an active Control condition and improves English skills and works at the same time on concentration, learning and memory abilities. The clients will gain some of the abilities and skills they might have lost or developed weaknesses in due to their abduction. AC will be applied in eight sessions (90-120min/session) in a standardized, manualized manner.

Sponsors

German Research Foundation
CollaboratorOTHER
University of Konstanz
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
12 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* clinical diagnosis of PTSD (Post-Traumatic Stress Disorder) derived from expert interviews * member of the group of formerly abducted people or former child soldiers

Exclusion criteria

* current substance dependence * mental retardation * psychotic disorder

Design outcomes

Primary

MeasureTime frame
Load of traumatic symptoms measured via the CAPS (Clinician-administered PTSD scale)3 months, 6 months and 1 year after completion of treatment

Secondary

MeasureTime frame
Load of depressive symptoms measured via the MINI, strength of suicidal ideation measured via the MINI, functionality measured via the CAPS, feelings of guilt measured via the CAPS, stigmatization measured via an adapted version of the PSQ3 months, 6 months and 1 year after completion of treatment

Countries

Uganda

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026