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Brief Integrative Therapy for Post-Traumatic Stress Disorder

Dartmouth Health logo

Dartmouth Health

Status

Completed

Conditions

Stress Disorders, Post-Traumatic

Treatments

Behavioral: Brief Integrative Therapy

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00047684
R21MH061319 (U.S. NIH Grant/Contract)
DSIR AT-AS

Details and patient eligibility

About

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.

Full 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.

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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