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Sponsored by: |
Bronx VA Medical Center |
Information provided by: | Bronx VA Medical Center |
ClinicalTrials.gov Identifier: | NCT00255554 |
Subjects will receive six months of DBT, consisting of one 90-minute group and one 60-minute individual session per week as well as telephone availability of the individual therapist. Half the subjects will concurrently receive escitalopram while half will receive placebo, in a randomized double-blind design.
Condition | Intervention |
Borderline Personality Disorder |
Behavioral: Dialectical Behavioral Therapy Drug: Escitalopram |
MedlinePlus related topics: | Personality Disorders |
Drug Information available for: | Escitalopram Benzetimide Citalopram Citalopram hydrobromide Dexetimide Escitalopram oxalate |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment |
Official Title: | Effects of Dialectical Behavioral Therapy and Escitalopram on Impulsive Aggression, Affective Instability and Cognitive Processing in Borderline Personality Disorder |
Ages Eligible for Study: | 18 Years to 60 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria: Is a male or female between 18 and 60 who meets criteria for Borderline Personality Disorder and has been off psychotropic medications for at least 2 weeks (6 weeks for fluoxetine).
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Exclusion Criteria: Meets criteria for Schizophrenia, Bipolar Disorder, Mental Retardation, current or recent Substance Dependence or a current Major Depressive Episode. Subjects also should not currently be in individual psychotherapy. (Case management and work therapy programs are allowed.)
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Contact: Emily Hart | 212-241-0441 | mpgroup@mssm.edu |
United States, New York | |||||
Bronx VA Medical Center | Recruiting | ||||
Bronx, New York, United States, 10029 |
Bronx VA Medical Center |
Principal Investigator: | Marianne Goodman, MD | Bronx VA Medical Center/Mount Sinai School of Medicine |
Study ID Numbers: | 3277-03-0027 |
First Received: | November 17, 2005 |
Last Updated: | November 17, 2005 |
ClinicalTrials.gov Identifier: | NCT00255554 |
Health Authority: | United States: Federal Government |
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