Comparing Treatments for Self-Injury and Suicidal Behavior in People With Borderline Personality Disorder

Suicide Clinical Trial

Official title:

Treating Suicidal Behavior and Self-Mutilation in Borderline Personality Disorder: Predictors of Change

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT00834834
• Other study ID #: #5752/6777R
• Secondary ID: R01MH061017R01MH
• Status: Recruiting
• Phase: Phase 4
• First received: February 2, 2009
• Last updated: September 25, 2013
• Start date: March 2009
• Est. completion date: August 2015

Study information

• Verified date: September 2013
• Source: New York State Psychiatric Institute
• Contact: Barbara H. Stanley, PhD
• Phone: 212-543-5918
• Email: bhs2[@]columbia.edu
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

This study will compare the effectiveness of two treatments, dialectical behavior therapy versus fluoxetine with clinical management, for reducing the risk of self-injury and suicidal behavior in people with borderline personality disorder.

Description:

Borderline personality disorder (BPD) is a chronic disorder in emotional regulation and is characterized by instability in self-image, mood, relationships, and behavior. People suffering from BPD have a high rate of self-injury and suicide attempts. This study will compare the effectiveness of two treatments for preventing self-injury and suicide in people with BPD: dialectical behavior therapy (DBT) and fluoxetine with clinical management. DBT is a behavioral therapy that teaches new coping skills to replace old strategies, including self-injury and attempted suicide. Fluoxetine is a selective serotonin reuptake inhibitor (SSRI) medication that has been used to treat BPD. Clinical management of fluoxetine, which is involved in administering the medication under normal conditions, refers to regular visits with a psychiatrist who will monitor medication effectiveness and side effects. Clinical management in this study may include adjusting the dosage of fluoxetine or prescribing a change in medication to citalopram, another SSRI.

Participation in this study will last 12 months, including all follow-up assessments. During the first study visit, participants will undergo baseline testing and be randomly assigned to receive either DBT or fluoxetine with clinical management. After a washout period, in which participants will transition off any medications they are currently taking, participants will receive 6 months of their assigned treatment. Participants receiving DBT will attend one 60-minute individual therapy session and one 90-minute group session every week. Participants assigned to the fluoxetine with clinical management condition will begin receiving 20 mg of fluoxetine daily and have their dose increased over the course of 4 weeks, based on tolerance, up to 40 mg. Participants assigned to fluoxetine may also be switched to citalopram, if the study psychiatrist thinks it will be more effective. Participants assigned to either fluoxetine or citalopram will undergo monthly blood tests to monitor the level of medication in their bodies.

Every 2 weeks, participants will undergo assessments of treatment effectiveness and side effects. After 2, 4, 6, 9, and 12 months, participants will undergo various neuropsychological tests and clinical interviews and self-report questionnaires about mood and life experiences. At study entry and at Weeks 12 and 24, participants will use a handheld computer to complete a week-long assessment of emotions. Fully healthy female participants will be asked to complete a functional magnetic resonance imaging (fMRI) scan, which will assess their ability to regulate emotions at the neural level. The fMRI scan and a stress test (for both men and women) will be performed at baseline and after 6 months.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 120
• Est. completion date: August 2015
• Est. primary completion date: August 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Meets DSM-IV criteria for borderline personality disorder (BPD)

• Attempted suicide in the past 2 months

• At least one additional suicide attempt, suicide-related behavior, or self-injury episode in the past year

• Current suicidal ideation

• Able to be managed as an outpatient

• Not currently receiving optimum psychiatric treatment and agrees to notify study staff if any psychiatric care outside this study is sought. If care other than that permitted by the protocol is utilized, participants can no longer be enrolled in the study.

• Has a stable living arrangement at study entry

• Speaks English

• Willing and judged to be clinically able to undergo wash-out of psychotropic medications, except for occasional benzodiazepine use, for 2 to 6 weeks before treatment

• Females must be willing to use an effective method of birth control.

Exclusion Criteria:

• Meets the DSM-IV criteria for mental retardation or the following disorders: bipolar I, schizophrenia, delusional disorder, schizophreniform disorder, schizoaffective disorder, or psychotic disorder not otherwise specified (NOS)

• Needs priority treatment for acute medical illness or other debilitating problem, such as severe substance dependence or anorexia

• Pregnant

• Clinically too unstable to be maintained as an outpatient

• Has clearly failed adequate trials of fluoxetine and citalopram for a major depression in the past 2 years

• History of severe allergies, adverse drug reactions, or known allergy to fluoxetine or citalopram

• Clinically inadvisable for the participant to end current treatment

• Heart pacemaker body implant; other metal implants, such as shrapnel or surgical prostheses; or paramagnetic objects contained within the body, as assessed via a metal screening questionnaire, which may present a risk to the participant or interfere with the fMRI scan

• Diagnosed with Raynaud's disorder

• History of hypertension, cardiovascular disease, or abnormal electrocardiograms (EKGs)

• Claustrophobia or significant discomfort in enclosed space

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Borderline Personality Disorder
• Personality Disorders
• Suicide

Intervention

Drug:
• Fluoxetine
Starting dose of 20 mg daily will increase over 4 weeks, depending on tolerability, up to 40 mg daily. Treatment will last 6 months.

Behavioral:
• DBT
One 60-minute individual therapy session and one 90-minute group therapy session every week. Treatment will last 6 months.

Drug:
• Citalopram
Dose set by study psychiatrist, up to 60 mg daily. Treatment will last 6 months.

Locations

Country	Name	City	State
United States	New York State Psychiatric Institute	New York	New York

Sponsors (2)

Lead Sponsor	Collaborator
New York State Psychiatric Institute	National Institute of Mental Health (NIMH)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Suicidal and self-injurious behavior		Measured after 6 months of treatment	Yes