Borderline Personality Disorder Clinical Trial
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
Verified date | December 2012 |
Source | Centre for Addiction and Mental Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Health Canada |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 180 |
Est. completion date | April 2009 |
Est. primary completion date | June 2007 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 60 Years |
Eligibility |
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 |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Canada | Centre for Addiction and Mental Health | Toronto | Ontario |
Canada | St Michael's Hospital | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
Centre for Addiction and Mental Health | Canadian Institutes of Health Research (CIHR), St. Michael's Hospital, Toronto |
Canada,
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* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Parasuicidal behaviour | intermittent | Yes | |
Secondary | Psychiatric hospitalization | intermittent | No | |
Secondary | Psychiatric symptoms | intermittent | No | |
Secondary | Treatment retention | intermittent | No |
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