Investigating the Mechanisms of Mindfulness-based Cognitive Therapy (MBCT)
- Conditions
- Major Depression (in Remission)
- Interventions
- Behavioral: Mindfulness-based Cognitive Therapy
- Registration Number
- NCT02226042
- Lead Sponsor
- University of Manchester
- Brief Summary
This research will investigate the neuropsychological mechanisms underlying the eight-week Mindfulness-based Cognitive Therapy (MBCT) programme.
Participants in remission from depression will be seen pre- and post-MBCT to assess the underlying neuropsychological mechanisms. All will be followed-up over 12 months to assess the relationship of these neuropsychological changes with relapse risk.
The research will focus primarily on changes in self-compassion, rumination, attention and structural brain changes, with secondary focus on other mechanisms of emotional processing and memory.
- Detailed Description
There will be three groups in total.
* The first group will take 36 participants in remission from major depression (rMDD) through the 8 week MBCT program.
* A control group of 36 rMDD participants will not receive the intervention.
* A group of never depressed healthy control participants will also be recruited.
Research visits for participants not undergoing MBCT will be separated by an 8 week gap.
All participants will be seen before and after the 8 weeks for completion of neuropsychological assessments and questionnaires.
rMDD participants will be followed up over the following 12 months to identify any predictors of relapse.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 112
Participants with remitted depression (rMDD):
- At least two previous episodes of DSM-IV major depression in adulthood, diagnosed using the Mini International Neuropsychiatric Interview (M.I.N.I).
- Full or partial remission for at least three months with two depressive episodes within the last five years.
- A score of less than or equal to 12 on the Montgomery Asberg Depression Rating Scale (MADRS) mood assessment.
- If on medication, no recent or planned major changes
Healthy volunteers:
- In good psychological health screened with the M.I.N.I
All participants:
- in good physical health (to reduce risk of confounding physical health problems).
- sufficiently fluent in English to ensure valid understanding and completion of the tasks.
- minimum I.Q level of 80 to ensure sufficient understanding of the neurocognitive tasks administered.
- colour vision and acuity within normal/corrected to normal limits.
Exclusion criteria:
- Any current mental health diagnosis (DSM-IV diagnosis including current major depression, bipolar disorder, psychosis, Obsessive Compulsive Disorder (OCD), substance abuse or dependence, eating disorders)
- Physical health or neurological disorders that might interfere with the interpretation of the tasks, including a history of significant head injury.
- In addition healthy volunteers will be without a history mental health disorders (DSM-IV)
- Current or previous experience of mindfulness-based treatments or extensive cognitive behavioural treatment, or planned participation in psychological treatments during the key time for the study (between pre and post visits).
- Planned major alteration in drug treatment for depression between pre and post visits.
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Mindfulness-based Cognitive Therapy Mindfulness-based Cognitive Therapy Individuals currently in remission from depression will choose to enter the Mindfulness-based Cognitive Therapy (MBCT) arm and undergo the 8 week MBCT group programme
- Primary Outcome Measures
Name Time Method Changes in self-compassion following MBCT measured by both neuropsychological and self-report measures measured at baseline and post intervention (8 weeks post baseline) and at each follow-up visit (3 in total) Two neuropsychological measures of self-compassion have been developed and will be administerat baseline and after MBCT/8 week gap (8 weeks post baseline). Self-report questionnaires will be administered before and after MBCT/8 week gap and at subsequent follow-up visits (3, 6, 12 months).
- Secondary Outcome Measures
Name Time Method Changes in levels of rumination following MBCT measured through both neuropsychological and self-report measures measured at baseline and after the intervention/8 week gap (8 weeks post baseline) and at each follow-up visit (3 in total) One neuropsychological measure of rumination has been developed and will be administered at baseline and immediately after MBCT/8 week gap (8 weeks post baseline).
Self-report questionnaires will be administered at baseline and after MBCT/8 week gap (8 weeks post baseline) and at subsequent follow-up visits (3,6,12 months).Changes in attention regulation following MBCT measured at baseline and after the intervention/8 week gap (8 weeks post baseline) Changes in brain structure following MBCT measured at baseline and after the intervention (8 weeks post baseline)
Trial Locations
- Locations (1)
University of Manchester
🇬🇧Manchester, Greater Manchester, United Kingdom