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Effectiveness of Cognitive Therapy for Suicide Attempters With Drug Dependence Disorder

This study is currently recruiting participants.
Study NCT00218725.   Last updated on April 2, 2007.   Information provided by National Institute of Mental Health (NIMH)

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Descriptive Information Fields
Brief Title  Effectiveness of Cognitive Therapy for Suicide Attempters With Drug Dependence Disorder
Official Title  Cognitive Therapy for Suicide Attempters With Drug Dependence Disorder
Brief Summary

This study will examine the effectiveness of combining cognitive therapy with enriched usual care for preventing subsequent suicide attempts in people with a drug dependence who have recently attempted suicide.

Detailed Description

Suicide attempts involving drug abuse are a major public health problem. Development of interventions that focus on reducing the suicide attempt rate among drug abusers is a necessity. There is a strong connection between drug abuse and both suicide attempts and completed suicide. As much as 45% of drug abusers have attempted suicide at least once. The rate of completed suicide among drug abusers has been reported to be as much as 30 times the rate for the general population. Unfortunately, there is a lack of empirically supported treatments for reducing suicidal behavior in drug abusers. This study will develop and evaluate the effectiveness of a cognitive therapy intervention for people with a drug dependence disorder who recently attempted suicide.

Participants in this single-blind study will be randomly assigned to one of two treatment groups: cognitive therapy combined with enriched usual care; or enriched usual care alone. An initial baseline assessment will occur within 7 days following the participant’s suicide attempt and subsequent medical evaluation at a hospital emergency department. Suicide behavior and ideation, depression, hopelessness, and addiction severity will be assessed. Following the baseline assessment, treatment will begin. The cognitive therapy treatment will be specifically developed to prevent suicide attempts. It will involve the identification of proximal thoughts, images, and core beliefs that were activated prior to the suicide attempt. Cognitive and behavioral strategies will be applied to address the identified thoughts and beliefs. Patients will also learn adaptive ways of coping with stressors. The enriched usual care will entail standard treatments for suicide prevention. Study visits will occur 1, 3, 6, 12, 18, and 24 months following enrollment. Baseline measurements will be repeated at each study visit to evaluate participants’ improvement. Participants receiving cognitive therapy will attend approximately 10 weekly or bi-weekly outpatient study visits. Participation will last for 2 years.

Study Phase Phase I
Study Type  Interventional
Study Design  Treatment, Randomized, Single Blind, Active Control, Parallel Assignment, Efficacy Study
Primary Outcome Measure  Suicidal Attempts, at Months 1, 3, 6, 12, 18, and 24
Secondary Outcome Measure  Suicide Ideation, at Months 1, 3, 6, 12, 18, and 24
Depression
Hopelessness
Substance Use
Condition  Suicide, Attempted
Substance-Related Disorders
Intervention  Behavioral: Cognitive Therapy
MEDLINE PMIDs
Links
Recruitment Information Fields
Recruitment Status  Recruiting
Enrollment  48
Start Date  May 2005
Completion Date
Eligibility Criteria 

Inclusion Criteria:

  • Recent suicide attempt with an emergency department visit within 48 hours of the attempt (suicide attempt is considered to be a potentially self-injurious behavior with a nonfatal outcome for which there is evidence, either explicit or implicit, that the individual intended to kill himself or herself)
  • Current DSM-IV diagnosis of a current drug dependence disorder within the past 6 months

Exclusion Criteria:

  • Self-mutilating behavior without intent to commit suicide
  • An acute, unstable, or severe Axis III disorder that may affect participation
Gender Both
Ages 18 Years and older
Accepts Healthy Volunteers No
Contacts ††
Contact: Gregory K. Brown, PhD     215-898-4104     gregbrow@mail.med.upenn.edu    
Location Countries  United States
Administrative Information Fields
NCT ID  NCT00218725
Organization ID P20 MH71905-02
Secondary IDs †† 802439, FWA00003616, DSIR 83-ATP
Study Sponsor  National Institute of Mental Health (NIMH)
Collaborators ††
Investigators 
Principal Investigator:     Aaron T. Beck, MD     University of Pennsylvania    
Principal Investigator:     Gregory K. Brown, PhD     University of Pennsylvania    
Information Provided By National Institute of Mental Health (NIMH)
Verification Date April 2007
First Received Date  September 21, 2005
Last Updated Date April 2, 2007

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




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