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A Randomized Controlled Clinical Trial With Orphans and Widows Who Experienced the Rwandan Genocide

Phase 1:Epidemiological Study of PTSD and Comorbid Disorders in Widows and Orphans Who Experienced the Rwandan Genocide Phase 2: A Randomized Controlled Clinical Trial With Orphans and Widows Who Experienced the Genocide Carried Out by Trained Local Psychologists -NET/IPT Versus Waiting List-

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00553956
Enrollment
150
Registered
2007-11-06
Start date
2007-08-31
Completion date
2009-02-28
Last updated
2007-11-06

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

Conditions

Depression, Posttraumatic Stress Disorder, Prolonged Grief Disorder

Brief summary

In the framework of the epidemiological study, local psychologists are trained in Butare in carrying out diagnostic interviews with orphans and widows who experienced the Rwandan genocide. With the aid of standardized questionnaires they will assess trauma related symptoms as well as Prolonged Grief Disorder. Under the supervision of clinical experts from the University of Konstanz the local psychologists will carry out a randomized house to house survey (Phase 1). As a second step, a controlled randomized clinical trial will be carried out. Local psychologists will be trained in applying Narrative Exposure Therapy and Interpersonal Psychotherapy. Genocide survivors that will be identified with a PTSD diagnosis will randomly be assigned to either the treatment condition or a waiting list. The treatment group will receive 5 individual sessions of NET in addition to 3 individual IPT sessions. Subsequent 3-months and 6-months post-tests will serve to evaluate the efficacy of this treatment module in alleviating trauma related symptoms and symptoms of prolonged grief. We expect a significant symptom reduction in the experimental group and no significant symptom reduction in the waiting list. After the 6-months post-test, the trained psychologists will train other psychologists in applying this treatment module under the supervision of clinical experts from the University of Konstanz. Afterwards, they will apply therapy to the victims from the waiting list. A 12-months follow-up will serve to evaluate the long-term effect of the NET/IPT combination.

Interventions

BEHAVIORALNarrative Exposure Therapy/Interpersonal Psychotherapy

The experimental group will receive 5 weekly individual sessions of NET in addition to 3 weekly individual sessions of IPT.

Sponsors

German Research Foundation
CollaboratorOTHER
University of Konstanz
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
17 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* widows and orphans * confrontation of the Rwandan genocide * clinical diagnosis of PTSD

Exclusion criteria

* mental retardation * psychotic symptoms * current drug or alcohol

Design outcomes

Primary

MeasureTime frame
Symptoms of PTSD, depression, prolonged grief disorder12 months

Countries

Rwanda

Contacts

Primary ContactSusanne Schaal, Dr.
Susanne.Schaal@gmx.de0049-(0)7531-880

Outcome results

None listed

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