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| Sponsor: | National Institute of Mental Health (NIMH) |
|---|---|
| Information provided by: | National Institute of Mental Health (NIMH) |
| ClinicalTrials.gov Identifier: | NCT00081367 |
Purpose
This study will determine the effectiveness of cognitive behavioral therapy (CBT) in preventing future suicide attempts in repeat suicide attempters.
| Condition | Intervention | Phase |
|---|---|---|
|
Suicide, Attempted |
Behavioral: CBT Behavioral: Standard care alone |
Phase III |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Community-Based Cognitive Therapy for Suicide Attempters |
| Estimated Enrollment: | 120 |
| Estimated Study Completion Date: | September 2009 |
| Estimated Primary Completion Date: | September 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Cognitive behavioral therapy (CBT) plus standard care |
Behavioral: CBT
Participants will receive ten weekly sessions of treatment. Suicidal thoughts or attempts, hopelessness, depression, health care utilization, and overall psychological and social adaptation will be assessed.
Behavioral: Standard care alone
Participants will receive standard care for suicide prevention.
|
| Active Comparator: Standard care alone |
Behavioral: Standard care alone
Participants will receive standard care for suicide prevention.
|
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.
Eligibility| Ages Eligible for Study: | 16 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
More Information
| Responsible Party: | Aaron T. Beck , MD, University of Pennsylvannia Medical School |
| ClinicalTrials.gov Identifier: | NCT00081367 History of Changes |
| Other Study ID Numbers: | R01 MH67805, DSIR 83-ATP |
| Study First Received: | April 9, 2004 |
| Last Updated: | October 5, 2010 |
| Health Authority: | United States: Federal Government |
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Minority Groups |
|
Suicide Suicide, Attempted Self-Injurious Behavior Behavioral Symptoms |