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Clinical Trials/NCT00081367
NCT00081367
Completed
Phase 3

Community-Based Cognitive Therapy for Suicide Attempters

University of Pennsylvania1 site in 1 country140 target enrollmentFebruary 2004

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Suicide, Attempted
Sponsor
University of Pennsylvania
Enrollment
140
Locations
1
Primary Endpoint
Repeat suicide attempts
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

This study will determine the effectiveness of cognitive behavioral therapy (CBT) in preventing future suicide attempts in repeat suicide attempters.

Detailed Description

Rates of mental health and substance use disorders are high among economically disadvantaged, ethnic minority populations. Studies have shown that CBT designed for this high-risk population is successful at reducing suicide attempts in people with suicidal thoughts or attempts. This study will implement a CBT intervention into the community and will focus on increasing compliance with psychiatric, substance abuse, and medical treatment. Participants in this study will be randomly assigned to receive either CBT plus standard care or standard care alone. Participants who receive CBT will have ten weekly sessions of treatment. Suicidal thoughts or attempts, hopelessness, depression, health care utilization, and overall psychological and social adaptation will be assessed. Assessments will be made 1, 3, 6, 12, 18, and 24 months after study completion.

Registry
clinicaltrials.gov
Start Date
February 2004
End Date
November 2009
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Gregory Brown

Research Associate Professor of Clinical Psychology in Psychiatry

University of Pennsylvania

Eligibility Criteria

Inclusion Criteria

  • Suicide attempt within 48 hours prior to being evaluated at the hospital
  • English speaking
  • Able to provide 2 verifiable contacts

Exclusion Criteria

  • Acute, unstable, or severe Axis III disorder or a severe Axis I disorder that may prevent safe participation in outpatient psychotherapy

Outcomes

Primary Outcomes

Repeat suicide attempts

Time Frame: Measured during treatment and 1, 3, 6, 12, 18, and 24 months after study completion

Study Sites (1)

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