Cognitive Behavioral Treatment for Post-Traumatic Stress Disorder in People With Additional Serious Mental Illnesses

Sponsor
Dartmouth-Hitchcock Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT00494650
Collaborator
National Institute of Mental Health (NIMH) (NIH)
200
5
2
40

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Cognitive behavioral therapy (CBT)
  • Behavioral: Brief PTSD treatment
N/A

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

Study Design

Study Type:
Interventional
Actual Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Cognitive Behavioral Treatment of Post-Traumatic Stress Disorder in Clients With Severe Mental Illness (in New Jersey)
Study Start Date :
Apr 1, 2008
Actual Primary Completion Date :
Jul 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

Participants will receive cognitive behavioral therapy.

Behavioral: Cognitive behavioral therapy (CBT)
CBT will include 12 to 16 counseling sessions, occurring weekly 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.

Active Comparator: 2

Participants will receive brief PTSD treatment.

Behavioral: Brief PTSD treatment
Brief PTSD treatment will include three weekly meetings with a therapist. Participants will learn about PTSD, how symptoms may be affecting their lives, and a technique for reducing anxiety associated with PTSD.

Outcome Measures

Primary Outcome Measures

  1. Knowledge of PTSD and effectiveness in correcting faulty, trauma-related beliefs [Measured post-treatment and at 6- and 12-month follow-ups]

  2. Depression, anxiety, and other psychiatric symptoms [Measured post-treatment and at 6- and 12-month follow-ups]

  3. PTSD diagnoses and symptom severity [Measured post-treatment and at 6- and 12-month follow-ups]

Secondary Outcome Measures

  1. 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]

  2. Quality of life and community functioning [Measured post-treatment and at 6- and 12-month follow-ups]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 United Behavioral HealthCare (UBHC): Partial Hospital Program Monmouth Junction New Jersey United States 08852
2 University Behavioral HealthCare (UBHC) Adult Outpatient Psychiatric Services New Brunswick New Jersey United States 08901
3 University Behavioral HealthCare (UBHC) Extended Treatment New Brunswick New Jersey United States 08901
4 University Behavioral HealthCare (UBHC) Extended Treatment Division - Adult Outpatient Psychiatric Services Newark New Jersey United States 07101
5 University Behavioral HealthCare (UBHC) Extended Treatment Division - Partial Hospital Program Newark New Jersey United States 07101

Sponsors and Collaborators

  • Dartmouth-Hitchcock Medical Center
  • National Institute of Mental Health (NIMH)

Investigators

  • Principal Investigator: Kim T. Mueser, PhD, Dartmouth-Hitchcock Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dartmouth-Hitchcock Medical Center
ClinicalTrials.gov Identifier:
NCT00494650
Other Study ID Numbers:
  • R01MH064662-02
  • R01MH064662-02
  • DSIR 83-ATIT
First Posted:
Jul 2, 2007
Last Update Posted:
Aug 8, 2012
Last Verified:
Aug 1, 2012

Study Results

No Results Posted as of Aug 8, 2012