- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02125942
Central Meditation and Imagery Therapy for Augmentation of Borderline Personality Disorder Treatment
Pilot Study of Central Meditation and Imagery Therapy for Borderline Personality Disorder
Borderline personality disorder is a severe psychiatric disorder marked by emotional instability, difficulty with interpersonal relationships, and self-harming behaviors. Despite receiving psychotherapy for borderline personality disorder, studies show that patient recovery is slow, and there is a high rate of self injury and suicide attempts early in treatment. There is thus a clear need to provide therapies to augment psychotherapy. We will conduct a pilot trial to determine whether a 6-week Central Meditation and Imagery Therapy (CMIT) is feasible for subjects with borderline personality disorder to undergo when added on to psychotherapy treatment. CMIT is a non-validated therapy that combines principles of mindfulness with meditation techniques and guided imagery. Sessions led by a trained clinician in a group setting once a week, and participants are asked to complete daily home practice.
The trial will involve 16 participants, all currently undergoing psychotherapy for borderline personality disorder. Participants will be randomly assigned to either a CMIT group that lasts 6 weeks, or a wait list group. Those in the wait list group will be able to receive CMIT after 6 weeks. All participants will continue to receive psychotherapy throughout the trial.
During the trial, we will also obtain preliminary data to help understand whether CMIT may result in psychological benefits for participants. This will include measuring the pulse in order to determine variation in beat to beat intervals of the heart during psychological tests, and filling out questionnaires before and after participation in CMIT.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
Los Angeles, California, United States, 90095
- University of California, Los Angeles
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Meeting the diagnostic criteria for BPD according to DSM-IV criteria
- Meeting the diagnostic criteria for BPD based on the Diagnostic Interview for Borderline - Revised
- Currently receiving psychotherapy.
- English language proficiency to understand written and oral communication
Exclusion Criteria:
- Active suicidality or suicidal intent as identified on the Columbia Suicide Severity Rating Scale
- Suicide attempt within the past month
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: meditation
Central Meditation and Imagery Therapy
|
mindfulness, guided imagery, meditation
|
|
No Intervention: wait list
waiting list
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Borderline Symptoms
Time Frame: 6 weeks
|
Borderline Symptom List
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Depression
Time Frame: 6 weeks
|
Quick Inventory of Depressive Symptoms
|
6 weeks
|
|
Anxiety
Time Frame: 6 weeks
|
Trait Anxiety Inventory
|
6 weeks
|
|
Positive Affect
Time Frame: 6 weeks
|
Positive and Negative Affect Scale
|
6 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heart rate variability
Time Frame: 6 weeks
|
Resting heart rate variability
|
6 weeks
|
Collaborators and Investigators
Investigators
- Principal Investigator: Felipe A Jain, MD, University of California, Los Angeles
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CMIT1044
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Borderline Personality Disorder
-
University of California, Los AngelesRecruitingBorderline Personality Disorder | Borderline Personality | BPD - Borderline Personality DisorderUnited States
-
University Hospital, Basel, SwitzerlandLeading House for the Latin American Region (Seed Money Grant SMG 1730)WithdrawnBorderline Personality Disorder (BPD)
-
Waypoint Centre for Mental Health CareRecruitingBorderline Personality Disorder (BPD)Canada
-
Mclean HospitalNot yet recruitingBorderline Personality Disorder (BPD)United States
-
University Hospital, MontpellierNot yet recruitingBorderline Personality Disorder | Borderline Personality Disorder (BPD)
-
Health Service Executive, IrelandCompletedPersonality Disorder, Borderline
-
University Hospital, ToulouseNot yet recruitingBorderline Personality Disorder (BPD) | Infusion of Ketamine in Severe Borderline Personality DisorderFrance
-
IRCCS Centro San Giovanni di Dio FatebenefratelliCompletedBorderline Personality Disorder (BPD)Italy
-
University of EdinburghCompletedEmotionally Unstable Personality Disorder, Borderline TypeUnited Kingdom
-
Hospital Universitari Vall d'Hebron Research InstituteUnknownBorderline Personality Disorder.Spain
Clinical Trials on Central Meditation and Imagery Therapy
-
University of California, San FranciscoCompleted
-
National Yang Ming Chiao Tung University HospitalCompleted
-
Nova Southeastern UniversityCompletedPost Traumatic Stress Disorder PTSDUnited States
-
Jordan University of Science and TechnologyCompletedStress, Psychological | Stress, Physiological | Stress ReactionJordan
-
University of Wisconsin, MadisonPatient-Centered Outcomes Research InstituteCompleted
-
Universiti Putra MalaysiaEuropean Society of Pediatric Gastroenterology, Hepatology and NutritionRecruitingTherapy | Physiology | Behaviour | PsychologyMalaysia
-
University Hospital, GenevaCompletedNightmares, REM-Sleep TypeSwitzerland
-
University of AmsterdamCompletedPosttraumatic Stress Disorder (PTSD)Netherlands
-
University Hospital, GenevaCompletedPTSD | Nightmares, REM-Sleep TypeSwitzerland