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NCT02125942 · ClinicalTrials.gov registry record · NA

Central Meditation and Imagery Therapy for Augmentation of Borderline Personality Disorder Treatment

A NA study, sponsored by University of California, San Francisco.

Completed
Registry status
NA
Development phase
15
Enrollment target

NCT02125942 is a NA study that has completed, run by University of California, San Francisco. The registered enrollment target is 15 participants.

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The verdict

NCT02125942, a NA study, has completed, sponsored by University of California, San Francisco.

COMPLETED
Registry status
NA
Development phase
15 participants
Enrollment target

Study Summary

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.

Interventions

  • BEHAVIORAL Central Meditation and Imagery Therapy

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2014-04
Est. Completion 2015-09
Phase NA

What the Registry Record Tells You About NCT02125942

The ClinicalTrials.gov registry entry for NCT02125942 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Central Meditation and Imagery Therapy is the first listed.

NCT02125942 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02125942 about?

NCT02125942 is a clinical study titled "Central Meditation and Imagery Therapy for Augmentation of Borderline Personality Disorder Treatment". 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 h...

What is the current status of trial NCT02125942?

This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2014-04. Estimated completion is 2015-09.

What interventions are being tested in trial NCT02125942?

The interventions under investigation include: Central Meditation and Imagery Therapy (BEHAVIORAL).

Who is sponsoring clinical trial NCT02125942?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

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