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Clinical Trials/NCT00494650
NCT00494650
Completed
Not Applicable

Cognitive Behavioral Treatment of Post-Traumatic Stress Disorder in Clients With Severe Mental Illness (in New Jersey)

Dartmouth-Hitchcock Medical Center5 sites in 1 country200 target enrollmentApril 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Post-Traumatic Stress Disorder
Sponsor
Dartmouth-Hitchcock Medical Center
Enrollment
200
Locations
5
Primary Endpoint
Knowledge of PTSD and effectiveness in correcting faulty, trauma-related beliefs
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

This study will evaluate the effectiveness of tailored cognitive behavioral therapy in treating post-traumatic stress disorder in people with additional mental illnesses.

Detailed Description

Post-traumatic stress disorder (PTSD) is an anxiety disorder that can develop after experiencing a terrifying event or ordeal in which grave physical harm occurred or was threatened. People with PTSD have persistent frightening thoughts and memories about the traumatic event and may experience sleep problems, feel detached or numb, or be easily startled. Studies have shown that PTSD occurs at high rates among people with serious mental illnesses (SMI), such as bipolar disorder, schizophrenia, and major depression. Research has also proven that cognitive behavioral therapy (CBT) is an effective PTSD treatment for caucasians living in rural areas when it is administered by a PhD-level clinician. It is not clear, however, how successful this treatment will be when it is delivered to a minority population by frontline mental health clinicians in an urban setting. This study will evaluate the effectiveness of tailored CBT in treating PTSD in people with additional mental illnesses who live in urban areas of New Jersey. Participants in this 4- to 5-month open-label study will be randomly assigned to receive either brief PTSD treatment or CBT. Participants assigned to brief PTSD treatment will have three meetings with a therapist per week. Participants will learn about PTSD, how symptoms may be affecting their lives, and a technique for reducing anxiety associated with PTSD. Participants assigned to CBT will attend 12 to 16 counseling sessions per week or every other week. Participants will learn about PTSD and ways to decrease anxiety associated with PTSD by completing homework assignments and practicing skills learned in counseling sessions. Outcomes will be assessed for all participants through interviews that will occur immediately post-treatment, 6 months post-treatment, and 1 year post-treatment. For information on a related study, please follow this link: http://clinicaltrials.gov/show/NCT00053690

Registry
clinicaltrials.gov
Start Date
April 2008
End Date
July 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Meets New Jersey definition of severe mental illness (SMI), which includes a DSM-IV diagnosis of an SMI; within the 3 to 6 months prior to study entry, functional limitations in major life activities that would be appropriate for the client's developmental stage; and within 2 years prior to study entry, two or more treatment episodes of greater intensity than outpatient services (such as inpatient, emergency, or partial hospitalization care, or a single episode lasting 3 months or more) OR a normal living situation disrupted to the point that supportive services were required to maintain the patient in their home or residence, or law enforcement officials were required to intervene
  • DSM-IV Axis I diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder, or major depression (as determined by Structured Clinical Interview)
  • Diagnosis of current severe PTSD at baseline assessment (as determined by a score greater than 65 on a Clinician Administered PTSD Scale)
  • Speaks English

Exclusion Criteria

  • Current diagnosis of alcohol or drug dependence
  • Hospitalization or suicide attempt in the past 2 months

Outcomes

Primary Outcomes

Knowledge of PTSD and effectiveness in correcting faulty, trauma-related beliefs

Time Frame: Measured post-treatment and at 6- and 12-month follow-ups

PTSD diagnoses and symptom severity

Time Frame: Measured post-treatment and at 6- and 12-month follow-ups

Depression, anxiety, and other psychiatric symptoms

Time Frame: Measured post-treatment and at 6- and 12-month follow-ups

Secondary Outcomes

  • Total cost for mental health and substance abuse treatment services utilization within the University Behavioral Health Care system(Measured post-treatment and at 6- and 12-month follow-ups)
  • Quality of life and community functioning(Measured post-treatment and at 6- and 12-month follow-ups)

Study Sites (5)

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