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Brief Integrative Therapy for Post-Traumatic Stress Disorder

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00047684
First Posted: October 16, 2002
Last Update Posted: September 10, 2013
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.
Collaborator:
National Institute of Mental Health (NIMH)
Information provided by:
Dartmouth-Hitchcock Medical Center
  Purpose
The purpose of this study is to refine Brief Integrative Therapy (BIT) and to evaluate its effectiveness in treating women with Post-Traumatic Stress Disorder (PTSD) following childhood sexual abuse. This study will also promote the development of skills that are necessary for increasing quality of life and improving self-esteem.

Condition Intervention
Stress Disorders, Post-Traumatic Behavioral: Brief Integrative Therapy

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Development and Initial Evaluation of Brief Integrative Therapy for PTSD

Resource links provided by NLM:


Further study details as provided by Dartmouth-Hitchcock Medical Center:

Estimated Enrollment: 20
Study Start Date: November 2001
Estimated Study Completion Date: November 2002
Detailed Description:

BIT integrates interpersonal, problem solving, affect regulation, and psychoeducational components. In this study, BIT is used to encourage women to focus on current issues and problems. The BIT therapist will help patients identify the impact of PTSD on their functioning, help them identify effective coping strategies for dealing with trauma-related distress, and encourage them to establish and maintain a certain degree of independence from the therapist.

Patients receive 15 weekly sessions of BIT. Assessments occur pre-treatment, post-treatment, and at a 3-month follow-up, and include self-report measures, clinician administered PTSD scale questions, interviews, and evaluations of lifetime stressors.

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Post-Traumatic Stress Disorder (PTSD) diagnosis
  • Childhood sexual abuse, defined as any sexual contact before the age of 16 with someone 5 or more years older
  • At least 1 clear, detailed memory of sexual abuse

Exclusion criteria:

  • Substance abuse or dependence
  • Psychotic disorder, bipolar disorder, or dissociative disorder
  • 2 or more suicidal or parasuicidal acts in the past year
  • Domestic violence involvement
  • Pregnancy or attempting to become pregnant
  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): NCT00047684


Locations
United States, Vermont
National Center for PTSD
White River Junction, Vermont, United States, 05001
Sponsors and Collaborators
Dartmouth-Hitchcock Medical Center
National Institute of Mental Health (NIMH)
  More Information

ClinicalTrials.gov Identifier: NCT00047684     History of Changes
Other Study ID Numbers: R21MH061319 ( U.S. NIH Grant/Contract )
DSIR AT-AS
First Submitted: October 11, 2002
First Posted: October 16, 2002
Last Update Posted: September 10, 2013
Last Verified: September 2008

Keywords provided by Dartmouth-Hitchcock Medical Center:
Child Abuse, Sexual

Additional relevant MeSH terms:
Stress Disorders, Traumatic
Stress Disorders, Post-Traumatic
Trauma and Stressor Related Disorders
Mental Disorders