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Clinical Trial Summary

The purpose of this study is to assess the efficacy of KIDNET versus a Meditation/Relaxation protocol in treating traumatized children when applied by locally trained teacher counsellors as well as the effectiveness and adequacy of such a treatment in a south-asian war affected stayee child community.


Clinical Trial Description

Outcome measures include PTSD symptom score, Depression score, Suicidal ideation and related functioning measures (including school grades) ;


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00564317
Study type Interventional
Source University of Konstanz
Contact
Status Completed
Phase Phase 3
Start date September 2004
Completion date January 2006

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