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Hope for the Chronically Suicidal Patient

This study is ongoing, but not recruiting participants.
Study NCT00154154.   Last updated on June 20, 2008.   Information provided by Centre for Addiction and Mental Health

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Descriptive Information Fields
Brief Title  Hope for the Chronically Suicidal Patient
Official Title  Hope for the Chronically Suicidal Patient: Evaluating the Clinical and Health Services Impact of Dialectical Behaviour Therapy in Individuals With Borderline Personality Disorder
Brief Summary

The aim of this study is to evaluate the clinical and cost effectiveness of Dialectical Behavior Therapy (DBT) for chronically suicidal behavior in individuals diagnosed with borderline personality disorder (BPD). Recent investigations of DBT have yielded positive results and have challenged the widely held opinion that the prognosis for this condition is poor. This study will consist of a two-arm randomized controlled trial that will compare DBT with a General Psychiatric Management (GPM) condition consisting of a structured algorithmic medication intervention plus psychosocial counseling. One-hundred and eighty participants will be randomly assigned to either DBT or to the GPM condition. Clinical outcomes will be assessed by changes in: (1) parasuicidal behaviour; (2) treatment retention; (3) psychiatric symptomatology; (4) anger expression; (5) social functioning and (6) health status. Cost outcomes will include an analysis of health service utilization. Clinical and cost evaluations will occur at 4-month intervals over the course of the one-year treatment and over a two-year follow-up.

Detailed Description

Suicide, a major cause of death worldwide, is a serious public health problem. Forty percent of individuals who commit suicide meet diagnostic criteria for a personality disorder and an even higher percent of those attempting suicide have a personality disorder . Borderline personality disorder (BPD) is highly associated with parasuicidal behaviour. Parasuicidal behaviour refers to suicide attempts or other self-injurious behaviour and is a risk factor for completed suicide. Approximately 69% - 80% of people diagnosed with BPD have committed at least one act of self-harm. Estimates of completed suicides in this population are about 9%, with this rate quadrupling for patients who meet 8 or more of the 9 DSM criteria for BPD.

Chronically suicidal behaviour in people with BPD is estimated to be among the most expensive psychiatric disorders to treat. While there is an extensive anecdotal literature on the treatment of this population, clinical outcomes have been dismal and treatment evidence based on well-designed trials is sparse. Dialectical Behavior Therapy (DBT), a broad-based cognitive-behavioral therapy (CBT), has recently shown promise in the treatment of this population. DBT is being widely adopted in the treatment of this disorder despite its limited empirical base. To date, there are few studies on DBT and no replications of the original research on DBT by researchers independent of the treatment developer.

The aim of this study is to evaluate the clinical and cost effectiveness of DBT for the treatment of parasuicidal individuals with BPD compared to a General Psychiatric Management (GPM) control condition involving a structured algorithm medication intervention plus psychosocial support. This study will compare the following outcome measures in participants who receive Dialectical Behavior Therapy versus General Psychiatric Management, Best Practices during a one-year treatment interval and two-year follow-up: (1) frequency and severity of parasuicidal behaviours ; (2) number of self-harm episodes (3) improvement in quality of life (4) cost effectiveness.

Hypotheses:(1) Patients in the DBT condition will show greater reductions in the frequency and severity of parasuicidal behaviours compared to patients in the GPM condition during a one-year treatment interval and two-year follow-up; (2) Compared to GPM, DBT will result in a greater reduction in the number of self-harm episodes and a greater improvement in quality of life but will have a higher direct cost. However, because DBT will result in significant offsetting reductions in other health service costs, the incremental cost-effectiveness ratios will fall within the range of many accepted medical interventions.

Study Phase
Study Type  Interventional
Study Design  Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Primary Outcome Measure  Parasuicidal behaviour [ Time Frame: intermittent ] [ Designated as safety issue: Yes ]
Secondary Outcome Measure  Psychiatric hospitalization [ Time Frame: intermittent ] [ Designated as safety issue: No ]
Psychiatric symptoms [ Time Frame: intermittent ] [ Designated as safety issue: No ]
Treatment retention [ Time Frame: intermittent ] [ Designated as safety issue: No ]
Condition  Borderline Personality Disorder
Intervention  Behavioral: General Psychiatric Management
Behavioral: Dialectical Behaviour Therapy
MEDLINE PMIDs 11665545,   6619404,   4066162,   3691077
Links Web page for the Centre for Addiction and Mental Health This link exits the ClinicalTrials.gov site
Recruitment Information Fields
Recruitment Status  Active, not recruiting
Enrollment  180
Start Date  October 2002
Completion Date September 2009
Eligibility Criteria 

Inclusion Criteria:

  • Meet DSM-IV criteria for BPD
  • Between 18-60 years of age
  • Have had two parasuicide episodes in the past five years with one occurring in the past 3 months
  • Have had OHIP coverage for 1 year or more
  • Literate in English
  • Provide informed consent to participate in the study

Exclusion Criteria:

  • Current active substance dependence disorder
  • Psychotic disorder,bipolar I disorder, or dementia
  • Evidence of an organic brain syndrome or mental retardation
  • A chronic or serious physical health problem that will require hospitalization within the next year (e.g. cancer)
  • A medical condition that would preclude the psychiatric medication regimen in the GPM condition
  • Definite plans to leave the province in the next 2 years
  • Currently engaged in DBT or GPM at St. Michael's Hospital
Gender Both
Ages 18 Years to 60 Years
Accepts Healthy Volunteers Yes
Contacts ††
Location Countries  Canada
Administrative Information Fields
NCT ID  NCT00154154
Organization ID CIHR: #200204MCT-101123
Secondary IDs †† CIHR: #200204MCT-101123
Study Sponsor  Centre for Addiction and Mental Health
Collaborators †† Canadian Institutes of Health Research (CIHR)
St. Michael's Hospital, Toronto
Investigators 
Principal Investigator:     Shelley F. McMain, PhD     Centre for Addiction and Mental Health    
Information Provided By Centre for Addiction and Mental Health
Verification Date June 2008
First Received Date  September 7, 2005
Last Updated Date June 20, 2008

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




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