Efficacy of Narrative Exposure Therapy (NET) in Treating Women After Human Trafficking or Forced Prostitution

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Martina Ruf, University of Konstanz
ClinicalTrials.gov Identifier:
NCT00717548
First received: July 15, 2008
Last updated: November 2, 2012
Last verified: November 2012
  Purpose

The purpose of this study is to perform an evaluation of a trauma-focused short-term intervention (Narrative Exposure Therapy; Schauer, M., Neuner, F. & Elbert, T.) on a variety of clinical outcome measures (PTSD, Depression, Somatic Complaints, Dissociation) in women after sexual exploitation and women trafficking.


Condition Intervention
Posttraumatic Stress Disorder
Depression
Dissociation
Behavioral: Narrative Exposure Therapy

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: The Effectiveness of Narrative Exposure Therapy in Treating Women After Trafficking and Forced Prostitution

Resource links provided by NLM:


Further study details as provided by University of Konstanz:

Primary Outcome Measures:
  • PTSD, Depression, Somatic Complaints, Dissociation [ Time Frame: Pre-Test, 4-weeks-Post-Test, 6-months-follow-up ] [ Designated as safety issue: No ]

Enrollment: 10
Study Start Date: June 2008
Study Completion Date: July 2011
Primary Completion Date: January 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: A Behavioral: Narrative Exposure Therapy
Trauma-Focused short term intervention (8-12 sessions)

  Eligibility

Ages Eligible for Study:   18 Years to 70 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Sexual Exploitation or Women Trafficked or Forced Prostitution
  • Symptoms of Post Traumatic Stress Disorder

Exclusion Criteria:

  • Current Psychotic Symptoms
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00717548

Locations
Germany
Research and Psychological Outpatient Clinic, University of Konstanz, Center for Psychiatry, House 22
Konstanz, Germany, 78479
Sponsors and Collaborators
University of Konstanz
  More Information

Additional Information:
No publications provided

Responsible Party: Martina Ruf, PhD, University of Konstanz
ClinicalTrials.gov Identifier: NCT00717548     History of Changes
Other Study ID Numbers: FH05.06.2008
Study First Received: July 15, 2008
Last Updated: November 2, 2012
Health Authority: Germany: Ethics Commission

Keywords provided by University of Konstanz:
Somatic Complaints

Additional relevant MeSH terms:
Depression
Depressive Disorder
Stress Disorders, Post-Traumatic
Stress Disorders, Traumatic
Dissociative Disorders
Behavioral Symptoms
Mood Disorders
Mental Disorders
Anxiety Disorders

ClinicalTrials.gov processed this record on August 20, 2014