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Clinical Trials/NCT00559000
NCT00559000
Completed
Phase 3

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

University of Konstanz1 site in 1 country25 target enrollmentDecember 2003
ConditionsPTSD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
PTSD
Sponsor
University of Konstanz
Enrollment
25
Locations
1
Primary Endpoint
PTSD-Symptoms according to the UCLA Child PTSD INDEX
Status
Completed
Last Updated
18 years ago

Overview

Brief Summary

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

Registry
clinicaltrials.gov
Start Date
December 2003
End Date
April 2006
Last Updated
18 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Konstanz

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

PTSD-Symptoms according to the UCLA Child PTSD INDEX

Time Frame: 1-month, 6-months, 12-months

Secondary Outcomes

  • 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)

Study Sites (1)

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