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Completed

NCT Number: NCT00559000

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

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

Completed

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Key information

Conditions

PTSD Mental Disorders Stress Disorders, Post-Traumatic Stress Disorders, Traumatic Trauma and Stressor Related Disorders

Age range

7 year–16 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

University of Konstanz, Research and Outpatient Clinic for Refugees

Reichenau-Lindenbühl, D-78479, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • none

Treatment and study plan

KIDNET

Behavioral

Narrative Exposure Therapy for Children

Primary outcomes

  1. PTSD-Symptoms according to the UCLA Child PTSD INDEX

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

Secondary outcomes

  1. 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

Sponsors and collaborators

Lead sponsor

University of Konstanz

Other

Collaborators

  • European Refugee Fund
  • German Research Foundation

Registry information

Important dates

Study start
2003
Study completion
2006
First posted
Nov 16, 2007
Registry last updated
Nov 16, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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