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Community-Based Cognitive Therapy for Suicide Attempters

Phase 3
Completed
Conditions
Suicide, Attempted
Interventions
Behavioral: CBT
Behavioral: Standard care alone
Registration Number
NCT00081367
Lead Sponsor
University of Pennsylvania
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
140
Inclusion Criteria
  • Suicide attempt within 48 hours prior to being evaluated at the hospital
  • English speaking
  • Able to provide 2 verifiable contacts
Read More
Exclusion Criteria
  • Acute, unstable, or severe Axis III disorder or a severe Axis I disorder that may prevent safe participation in outpatient psychotherapy
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Cognitive behavioral therapy (CBT) + standard careStandard care aloneParticipants will receive ten weekly sessions of treatment plus standard care for suicide prevention.
Cognitive behavioral therapy (CBT) + standard careCBTParticipants will receive ten weekly sessions of treatment plus standard care for suicide prevention.
Standard care aloneStandard care aloneParticipants will receive standard care for suicide prevention.
Primary Outcome Measures
NameTimeMethod
Repeat suicide attemptsMeasured during treatment and 1, 3, 6, 12, 18, and 24 months after study completion
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Pennsylvania

🇺🇸

Philadelphia, Pennsylvania, United States

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