Evaluation of a Modified Dialectical Behavior Therapy Program

This study is currently recruiting participants. (see Contacts and Locations)
Verified May 2014 by University of Manitoba
Sponsor:
Information provided by (Responsible Party):
University of Manitoba
ClinicalTrials.gov Identifier:
NCT01635556
First received: May 23, 2012
Last updated: May 22, 2014
Last verified: May 2014

May 23, 2012
May 22, 2014
September 2012
December 2014   (final data collection date for primary outcome measure)
  • Quality of Life Enjoyment and Satisfaction Questionnaire [ Time Frame: Baseline ] [ Designated as safety issue: No ]
    This measure assesses the degree of enjoyment and satisfaction experienced during the past week in several areas: physical health, feelings, work, household duties, school, leisure time, and social relationships.
  • Quality of Life Enjoyment and Satisfaction Questionnaire [ Time Frame: Change - baseline to 6 months ] [ Designated as safety issue: No ]
    This measure assesses the degree of enjoyment and satisfaction experienced during the past week in several areas: physical health, feelings, work, household duties, school, leisure time, and social relationships.
  • Quality of Life Enjoyment and Satisfaction Questionnaire [ Time Frame: Change - 6 months to 12 months ] [ Designated as safety issue: No ]
    This measure assesses the degree of enjoyment and satisfaction experienced during the past week in several areas: physical health, feelings, work, household duties, school, leisure time, and social relationships.
  • Quality of Life Enjoyment and Satisfaction Questionnaire [ Time Frame: Change - 12 months to 18 months ] [ Designated as safety issue: No ]
    This measure assesses the degree of enjoyment and satisfaction experienced during the past week in several areas: physical health, feelings, work, household duties, school, leisure time, and social relationships.
Same as current
Complete list of historical versions of study NCT01635556 on ClinicalTrials.gov Archive Site
  • Borderline Symptom List 23 [ Time Frame: Baseline ] [ Designated as safety issue: No ]
  • Borderline Symptom List 23 [ Time Frame: Change - baseline to 6 months ] [ Designated as safety issue: No ]
  • Borderline Symptom List 23 [ Time Frame: Change - 6 months to 12 months ] [ Designated as safety issue: No ]
  • Borderline Symptom List 23 [ Time Frame: Chabge - 12 months to 18 months ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Evaluation of a Modified Dialectical Behavior Therapy Program
Evaluation of a Modified Dialectical Behavior Therapy Program for Borderline Personality Disorder

The goal of this pilot project is to offer outpatient Dialectical Behavior Therapy (DBT) treatment as described in Linehan's text (1993), which is considered an effective treatment of borderline personality disorder. This treatment consists of weekly individual psychotherapy, weekly group skills training, 24 hour telephone consultation, and weekly team consultation meetings for therapists. The investigators program is able to offer all of these components except the 24 hour phone consultation (which has been modified due to employment/union guidelines of interdisciplinary staff working within the investigators health care system). This project intends to offer the treatment for a period of 6 months.

As such, this proposed research project seeks to assess the feasibility of implementing an outpatient DBT program within a public health care setting in Canada. This study also aims to evaluate this DBT program for clinical effectiveness in its modified format. Specifically, the investigators will examine relevant outcomes related to patient functioning (e.g., depression, self-harm and suicidal behaviors, and admissions to hospital/ER visits) and improvement (e.g., improved quality of life, meeting work/employment goals) pre and post completion of this 6 month treatment program.

The investigators hypotheses are that each patient will show improvement in all outcome variables (e.g., improved mood and quality of life, decreased self-harm, decreased ER visits and hospitalization visits, etc). The investigators also hypothesize that the investigators modified program will produce comparable results to those from studies of standard outpatient DBT.

Standard DBT includes four modes of intervention: weekly individual psychotherapy; weekly skills group; 24 hour phone consultation to the patient; and consultation team meetings. The skills group is focused on teaching skills (mindfulness, emotional regulation, distress tolerance, and interpersonal effectiveness), and facilitating the replacement of maladaptive behaviors with adaptive behaviors (Neasciu, Rizvi, & Linehan, 2010). Individual therapy sessions focus on reducing target problem behaviors (e.g., life threatening behavior, therapy interfering behavior, quality of life interfering behaviors). Phone consultation is to aid the client in generalizing skill use to their every day life. The consultation team meetings are for the therapists, to provide support, and to aid therapists in staying adherent to a DBT frame of treatment.

This project will be utilizing a convenience sample. Patients are referred to the program by their psychiatrist/family doctor. They are assessed by a Clinical Psychologist to determine if they meet criteria for a diagnosis of Borderline Personality Disorder via clinical interview and a semi-structured diagnostic interview. They must also meet the inclusion/exclusion criteria for participation in the program, which are as follows:

Inclusion Criteria

  • 18 years or older
  • Borderline personality disorder diagnosis
  • Chronic suicidal ideation or parasuicidal acts, or other self-destructive, impulsive behaviors
  • Must be willing to sign DBT contract and commit to 6-month duration of treatment of both individual therapy and skills training group.

Exclusion Criteria

  • Active psychosis
  • Severe developmental delays, cognitive impairment or learning disabilities
  • No violent behaviors will be tolerated. Patients with a history of dangerous or aggressive behaviors towards others, history of medical harm to previous therapists may not be considered.

Following this, they must agree to participate in the program and to the program requirements (weekly individual therapy, skills group, etc). Once this has occurred, they will be approached by a research assistant to discuss with them their voluntary participation in this research study. Once consent is provided, the patient will complete several baseline measures. These same measures will be completed at post treatment (6 months) and then again at 12 months and 18 months for follow-up. Each patient will also complete a weekly diary card, which asks them to record several aspects of daily functioning, as well as self-harm urges and behaviors, and use of skills taught in DBT.

Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample

The participants will be selected from the community.

Borderline Personality Disorder
Behavioral: Dialectical Behavior therapy
Weekly psychotherapy of both individual and group sessions
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
24
December 2014
December 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Diagnosis of Borderline Personality Disorder
  • Chronic suicidal ideation or parasuicidal acts, or other self-destructive, impulsive behaviors
  • Must be enrolled in dialectical behavior therapy program

Exclusion Criteria:

  • Active psychosis
  • Severe developmental delays, cognitive impairment or learning disabilities
  • History of or current violent/aggressive behaviors
Both
18 Years to 65 Years
No
Contact: Valerie Krysanski, PHD 2044773119 vkrysanski@vgh.mb.ca
Canada
 
NCT01635556
H2012:128
Yes
University of Manitoba
University of Manitoba
Not Provided
Principal Investigator: Valerie Krysanski, PHD University of Manitoba
University of Manitoba
May 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP