- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05111665
Decentering and Relapse/Recurrence in MBCT for Depression in Adults
The Association Between Decentering and Reductions in Relapse/Recurrence in Mindfulness-Based Cognitive Therapy for Depression in Adults: A Randomized Controlled Trial
Objective: "Decentering" is defined as the ability to observe one's thoughts and feelings as temporary, objective events in the mind, and is increasingly regarded as a candidate mechanism in mindfulness-based interventions. The current study sought to examine the role of decentering, and other related variables, in the efficacy of Mindfulness-based cognitive therapy (MBCT) as compared to two active comparison conditions.
Method: Formerly depressed individuals (N = 227), randomly assigned to MBCT (n = 74), relaxation group therapy (RGT; n = 77) or treatment-as-usual (TAU; n = 76), completed self-report measures of decentering and symptoms of depression at pre-, mid-, and post-treatment, and relapse was assessed at 3, 6, 9, and 12 months, post-treatment.
Study Overview
Status
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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British Columbia
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Vancouver, British Columbia, Canada, V6J 5C6
- Mark Lau
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- a Diagnostic and Statistical Manual of Mental Disorders (4th ed.; DSM IV-TR; American Psychiatric Association (APA), diagnosis of major depressive disorder (MDD) without psychotic features, in Full Remission;
- three or more prior major depressive episodes;
- age between 18 and 65 years;
- cognitive reactivity (CR) or mood-activated dysfunctional beliefs score greater than or equal to eight (see assessment procedure below);
- a score of less than 10 on the Hamilton Rating Scale for Depression (HRSD);
- minimum of a 10 week period free of psychotropic medication other than stable dosage of antidepressant medication for a minimum of four weeks;
- fluency in English; An increased cognitive reactivity score of eight points or more and,
- ability to give informed consent and complete questionnaires unassisted.
Exclusion Criteria:
- a diagnosis of bipolar disorder (past or present), schizophreniform disorders, substance abuse or dependence (current or within the past six months), borderline or antisocial personality disorder, or neurocognitive disorders;
- current psychotherapy or counselling more frequently than twice per month;
- current practice of meditation more than once per week or yoga more than twice per week;
- electroconvulsive therapy within the past six months; or
- self-reported ingestion of alcohol or other psychoactive substances within the past 48 hrs.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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EXPERIMENTAL: Mindfulness-based Cognitive Therapy (MBCT)
Remitted depressed participants received eight-weekly, two-hour MBCT sessions (Segal et al., 2013).
This program combines MBSR meditation practices (e.g., body scan, mindful stretching, mindfulness of breath/body/sounds/thoughts) with traditional CT techniques (e.g., psychoeducation about depression symptoms and automatic thoughts, exercises designed to demonstrate how the nature of one's thoughts change with one's mood, questioning of automatic thoughts and creating a relapse prevention plan).
Finally, participants engaged in a daily meditation practice and homework exercises directed at integrating the application of awareness skills into daily life.
Each MBCT group was led by a masters-level clinician who was an active MBCT/Mindfulness-Based Stress Reduction (MBSR) instructor.
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ACTIVE_COMPARATOR: Relaxation Group Therapy (RGT)
The revised edition of the Changeways Relaxation Programme (Paterson, 1997) served as the active control condition to control for non-specific group factors including group participation, expectation of change or therapeutic contact and attention.
The rationale was that relaxation can be used to better manage life stressors which precipitate depressive episodes.
Participants received eight-weekly, two-hour relaxation training sessions.
This group program combines psychoeducation regarding the effects of stress, diaphragmatic breathing, progressive muscle relaxation, passive relaxation and imagery.
It also incorporates time for participants to discuss the events of the week to facilitate the supportive aspect of group participation.
Finally, participants were asked to engage in daily exercises to practice the various relaxation strategies.
Each RGT group was led by a doctoral-level therapist.
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PLACEBO_COMPARATOR: Treatment as usual (TAU)
Participants randomized to the TAU group were instructed that participants would receive MBCT at the end of the follow-up period and to seek help from their family doctors or other sources as the normally would, should the participants encounter symptomatic deterioration or other difficulties over the course of the study.
At the end of the follow-up phase, participants in the TAU and RGT group were offered the opportunity to receive MBCT.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Major depressive disorder (MDD) relapse/recurrence - incidence of
Time Frame: 12- month post-treatment follow-up
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Number of participants meeting criteria for relapse/recurrence of MDD during follow-up
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12- month post-treatment follow-up
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Change in major depressive disorder (MDD) relapse/recurrence - time to relapse/recurrence
Time Frame: 3-, 6-, 9-, and 12- month post-treatment follow-up
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Change in relapse/recurrence of MDD (i.e., survival) across follow-up
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3-, 6-, 9-, and 12- month post-treatment follow-up
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change in Beck Depression Inventory - Second Edition total scores
Time Frame: Pre-, mid- (i.e., at week 4 of MBCT), and post-treatment (i.e., after 8 weeks of MBCT)
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Change in symptoms of depression across MBCT treatment
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Pre-, mid- (i.e., at week 4 of MBCT), and post-treatment (i.e., after 8 weeks of MBCT)
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Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H07-03046
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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