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NCT00252031 Clinical Trial

DBT in Borderline Personality Disorder

Borderline Personality Disorder Clinical Trial

Official title:
Dialectical Behavioral Therapy for Patients With Borderline Personality Disorder

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00252031
Other study ID # 3277-02-0002
Secondary ID
Status Recruiting
Phase N/A
First received November 9, 2005
Last updated November 17, 2005

Study information
Verified date November 2005
Source Bronx VA Medical Center
Contact Emily Hart
Phone 212-241-0441
Email mpgroup@mssm.edu
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

Subjects will receive a 6-month course 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.

Recruitment information / eligibility
Status Recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: Is a male or female between 18 and 60 who meets criteria for Borderline Personality Disorder and has had at least 2 prior instances of suicidal or parasuicidal behavior. Either is off psychotropic drugs or is on a stable medication regimen. (During the study, psychotropic medications will be prescribed by a psychiatrist in the Mood and Personality Disorders Group.)

Exclusion Criteria: Meets criteria for Schizophrenia, Bipolar Disorder, Mental Retardation or current or recent Substance Dependence. Subjects also should not currently be in individual psychotherapy. (Case management and work therapy programs are allowed.)

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• Dialectical Behavioral Therapy

Locations
Country Name City State
United States Bronx VA Medical Center Bronx New York

Sponsors (1)
Lead Sponsor Collaborator
Bronx VA Medical Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Measures of parasuicidal behavior, suicidal ideation, mood and emotion, dissociation and health care utilization at baseline, 3 months, 6 months and 9 months
Secondary Measures of cognitive processing at baseline and 6 months
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