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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00559000
First Posted: November 16, 2007
Last Update Posted: November 16, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborators:
European Refugee Fund
German Research Foundation
Information provided by:
University of Konstanz
  Purpose
The purpose of the study is to assess the effectiveness of KIDNET in treating traumatized refugee children in Germany

Condition Intervention Phase
PTSD Behavioral: KIDNET Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Investigator)
Primary Purpose: Treatment
Official Title: The Efficacy of KIDNET in the Treatment of Traumatized Refugee Children in Germany

Further study details as provided by University of Konstanz:

Primary Outcome Measures:
  • PTSD-Symptoms according to the UCLA Child PTSD INDEX [ Time Frame: 1-month, 6-months, 12-months ]

Secondary Outcome Measures:
  • Cognitive Performance according to SPM, CPM, Rey-Figure-Test, d2; Other mental health disorders according to M.I.N.I.-KID [ Time Frame: 6-months, 12-months ]

Enrollment: 25
Study Start Date: December 2003
Study Completion Date: April 2006
Arms Assigned Interventions
No Intervention: Waitinglist Control
Experimental: KIDNET Behavioral: KIDNET
Narrative Exposure Therapy for Children

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   7 Years to 16 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

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

Exclusion Criteria:

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00559000


Locations
Germany
University of Konstanz, Research and Outpatient Clinic for Refugees
Reichenau-Lindenbühl, Germany, D-78479
Sponsors and Collaborators
University of Konstanz
European Refugee Fund
German Research Foundation
Investigators
Principal Investigator: Thomas Elbert, Prof. Dr. University of Konstanz
Principal Investigator: Martina Ruf, Dipl.-Psych. University of Konstanz
  More Information

Additional Information:
ClinicalTrials.gov Identifier: NCT00559000     History of Changes
Other Study ID Numbers: mb
First Submitted: November 15, 2007
First Posted: November 16, 2007
Last Update Posted: November 16, 2007
Last Verified: November 2007

Keywords provided by University of Konstanz:
PTSD
Children
trauma-focused Treatment
KIDNET
Narrative Exposure Therapy for Children