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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00893750
Other study ID # NE1390/2.1_UKon
Secondary ID
Status Completed
Phase N/A
First received May 4, 2009
Last updated June 30, 2010
Start date May 2009

Study information

Verified date June 2010
Source University of Konstanz
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

More than 300,000 children are fighting in armed conflicts all over the world. In Uganda an estimated number of 25,000 children have been abducted and forced to fight or work as porters and sex slaves on the side of the rebels during the conflict between the Lord's Resistance Army (LRA) and the Ugandan government. Each year, thousands of former child soldiers have returned to their communities after they had fled or were freed from the rebels. It is well known that a high percentage of these youths are suffering from mental health problems. This could be one of the possible reasons why they are facing difficulties to reintegrate into their communities.

The main aim of the proposed project is two-fold. On the one hand, the investigators want to systematically explore the relationship between mental health and important variables for reintegration into the communities like aggression, hostility, feelings of revenge, compromises and conflict behaviour and readiness for reconciliation in formerly abducted and other vulnerable youth (orphans, child mothers and handicapped youths) in Northern Uganda. On the other hand, the investigators want to probe the efficacy of existing and newly developed interventions for formerly abducted and other vulnerable youths that are supposed to foster their mental well-being as well as their reintegration into the society and therewith are part of the long-term prevention of new conflicts in Northern Uganda.


Recruitment information / eligibility

Status Completed
Enrollment 600
Est. completion date
Est. primary completion date June 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 12 Years to 30 Years
Eligibility Inclusion Criteria:

- for individual NET Treatment: PTSD diagnosis

- for group interventions: all youths in the selected vocational training centres will be included

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
NET Truth Education
Individual Narrative Exposure and Truth Education in Groups
Conflict Resolution and Social Competence Skills
Conflict Resolution and Social Competence Skills in Groups
Traditional Ways of Coping
Methods Collected by Local Teachers to Help Vulnerable Children and Youths in Northern Uganda

Locations

Country Name City State
Uganda Vivo Gulu & Kitgum

Sponsors (1)

Lead Sponsor Collaborator
University of Konstanz

Country where clinical trial is conducted

Uganda, 

Outcome

Type Measure Description Time frame Safety issue
Primary PTSD Symptoms and Functional Level 6-months and 12-months follow-up No
Secondary Aggression Reconciliation Re-Integration Conflict and Compromise Behaviour 6-months and 12-months follow-up No
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