PTSD Clinical Trial
Official title:
The Efficacy of KIDNET in the Treatment of Traumatized Refugee Children in Germany
| Verified date | November 2007 |
| Source | University of Konstanz |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Germany: Ethics Commission |
| Study type | Interventional |
The purpose of the study is to assess the effectiveness of KIDNET in treating traumatized refugee children in Germany
| Status | Completed |
| Enrollment | 25 |
| Est. completion date | April 2006 |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 7 Years to 16 Years |
| Eligibility |
Inclusion Criteria: - refugee children - age range: 7-16 - PTSD-Diagnosis Exclusion Criteria: |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Germany | University of Konstanz, Research and Outpatient Clinic for Refugees | Reichenau-Lindenbühl |
| Lead Sponsor | Collaborator |
|---|---|
| University of Konstanz | European Refugee Fund, German Research Foundation |
Germany,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | PTSD-Symptoms according to the UCLA Child PTSD INDEX | 1-month, 6-months, 12-months | ||
| Secondary | 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 |
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