The Efficacy of KIDNET in the Treatment of Traumatized Refugee Children in Germany

Phase 3

Completed

• Conditions: PTSD

• Registration Number: NCT00559000
• Lead Sponsor: University of Konstanz

Brief Summary

The purpose of the study is to assess the effectiveness of KIDNET in treating traumatized refugee children in Germany

Detailed Description

Not available

Study Timeline

• Study Start: 2003-12
• Study Completion: 2006-04
• Status Verified: 2007-11
• Study First Submitted: 2007-11-15
• Study First Submitted QC: 2007-11-15
• Last Update Submitted: 2007-11-15
• Study First Posted: 2007-11-16
• Last Update Posted: 2007-11-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

• refugee children
• age range: 7-16
• PTSD-Diagnosis

Exclusion Criteria

• none

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
PTSD-Symptoms according to the UCLA Child PTSD INDEX	1-month, 6-months, 12-months

Secondary Outcome Measures

Name	Time	Method
Cognitive Performance according to SPM, CPM, Rey-Figure-Test, d2; Other mental health disorders according to M.I.N.I.-KID	6-months, 12-months

Trial Locations

Locations (1)

University of Konstanz, Research and Outpatient Clinic for Refugees; 🇩🇪 Reichenau-Lindenbühl, Germany

University of Konstanz, Research and Outpatient Clinic for Refugees

🇩🇪Reichenau-Lindenbühl, Germany