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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01193205
Other study ID # 050/2010
Secondary ID
Status Completed
Phase Phase 1
First received August 31, 2010
Last updated May 25, 2016
Start date July 2010
Est. completion date December 2012

Study information

Verified date May 2016
Source Centre for Addiction and Mental Health
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the effectiveness of a 20-week Dialectical Behaviour Therapy (DBT) skills training group for the treatment of chronic suicidal and non-suicidal self-injurious (NSSI) behaviours in individuals diagnosed with borderline personality disorder (BPD). Previous research has established the effectiveness of a one year comprehensive, combined individual and group DBT treatment. However, in practice, DBT is often offered in a skills only group format. This study will consist of a randomized, controlled trial designed to evaluate the effectiveness of DBT compared to a wait list control. 84 participants will be randomized to the 20-week DBT group or the wait-list and the following outcomes will be assessed:

1. frequency of suicidal and NSSI behaviours

2. symptom distress

3. impulsivity

4. treatment retention

5. skill acquisition and

6. social functioning

Assessments will occur at pre-treatment, 10 weeks, 20 weeks and 3 months post treatment. The following main hypotheses will be examined: (1) Patients in the DBT skills group condition will have superior outcomes to patients on the treatment as usual wait list control in areas targeted by the treatment: frequency of suicidal and NSSI behaviours, emergency room visits, psychiatric hospital admissions, impulsivity, and knowledge and use of behavioral skills, general symptoms. The group receiving DBT will have superior outcomes at post treatment and these outcomes will be maintained during the three month post-treatment follow-up.


Description:

The study will consist of a single-blind, two-arm randomized controlled trial designed to evaluate the effectiveness of DBT skills group offered as an adjunct to treatment as usual compared to a wait list control plus treatment as usual. The continuation of treatment as usual in both arms is permitted for two reasons. First, it would be unethical to assign suicidal patients to a wait list condition that prohibited involvement in ongoing treatment. Second, the proposed design enables us to address the question of the additive effect of the DBT skills group intervention. Subjects will be randomized to receive 20 weeks of DBT group skills training plus treatment as usual, or to a wait list control plus treatment as usual. Clinical effectiveness outcomes will be assessed at baseline, at 10 weeks, at 20 weeks and at 8 months follow-up. DBT skills training is a manualized intervention developed by Linehan (1993). Key skills from the modules described in Miller, Rathus, and Linehan (2006) will serve as the basis of the DBT skills group, delivered in a psychoeducational format over the course of weekly two-hour sessions. The skills group covers five modules: mindfulness, emotion regulation, distress tolerance, interpersonal effectiveness, and dialectics.


Recruitment information / eligibility

Status Completed
Enrollment 84
Est. completion date December 2012
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- diagnosis of DSM-IV Borderline Personality Disorder

- 18-60 years of age

- have had two suicidal or non-suicidal self-injurious behaviours in the past five years with one occurring in the past ten weeks

- be literate in English

- provide informed consent to participate in the study.

Exclusion Criteria:

- not meet DSM-IV criteria for a psychotic disorder, bipolar disorder or, dementia

- not have evidence of an organic brain syndrome or mental retardation based on clinical interview

- not participated in DBT treatment during the past year

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Skills Training
20 weeks of Dialectical Behaviour Therapy Skills Training

Locations

Country Name City State
Canada Centre for Addiction and Mental Health Toronto Ontario

Sponsors (2)

Lead Sponsor Collaborator
Centre for Addiction and Mental Health Ontario Mental Health Foundation

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Deliberate Self-harm Inventory (DSHI; Gratz, 2001) and Lifetime Suicide Attempt Self-Injury interview (LSASI; formerly Lifetime Parasuicide Count, Linehan MM, Comtois KA, unpublished manuscript, 1996) Self-report measures assessing self-harm and suicidal behaviour baseline; 10 weeks; 20 weeks; 3 month follow up Yes
Secondary Treatment History Interview (THI-2; Linehan & Heard, 1987) Assesses for emergency and psychiatric hospitalizations baseline; 10 weeks; 20 weeks; 3 month follow up No
Secondary Barett Impulsiveness Scale (BIS-11; Patton et al., 1995) Self-report measure assessing for impulsive behaviour Baseline; 10 weeks; 20 weeks; 3 months follow up No
Secondary The State-trait Anger Expression Inventory (STAXI; Spielberger, Krasner & Solomon, 1988) Self-report assessing for anger expressions Baseline; 10 weeks; 20 weeks; 3 months Follow up No
Secondary The Borderline Evaluation of Severity over time Scale (BEST; Phfolm & Bloom, 1997) self-report measure assessing for severity of BPD symptoms Baseline; 10 weeks; 20 weeks; 3 months Follow up No
Secondary The Symptom Checklist 90 - Revised (SCL-90-R; Derogatis, 1983) Self-report measure assessing for various psychiatric symptoms Baseline; 10 weeks; 20 weeks; 3 months Follow up No
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