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Clinical Trials/NCT02457936
NCT02457936
Completed
Not Applicable

Examining Cognitive Mechanisms of Clinical Improvement Following Mindfulness Based Cognitive Therapy for Depressed Individuals

Massachusetts General Hospital1 site in 1 country52 target enrollmentApril 2015
ConditionsDepression

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Depression
Sponsor
Massachusetts General Hospital
Enrollment
52
Locations
1
Primary Endpoint
Change from baseline in depressive symptoms as measured by the Hamilton Depression Rating Scale
Status
Completed
Last Updated
last year

Overview

Brief Summary

Depression one of the leading causes of disability worldwide. Individuals suffering from depression typically exhibit impairments in various mental abilities, such as the ability to effectively direct and control attention and the ability to switch between thinking about different things and concepts (commonly referred to as "cognitive flexibility").

Mindfulness meditation training is a technique which involves focusing one's awareness on the present moment, while calmly acknowledging and accepting one's feelings, thoughts, and bodily sensations. It has been well documented to improve depressive symptoms and prevent recurrence of depressive episodes, yet little is known about how mindfulness does so and what are the underlying mental mechanisms involved. Here the investigators propose to examine the efficacy of an 8-week mindfulness training program in improving the ability to direct and control attention, as well as in cognitive flexibility.

Individuals diagnosed with recurrent depression will undergo an 8-week mindfulness training program. Participants' depressive symptoms as well as their performance on measures of attention and cognitive flexibility will be examined. Participants will be assigned to mindfulness training or a wait-list control group. Half of the participants will be examined before and after the mindfulness training program and the other half will be tested 8-weeks apart and then begin their training.

Registry
clinicaltrials.gov
Start Date
April 2015
End Date
April 2016
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jonathan Greenberg

Postdoctoral research fellow

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Reporting dysphoria for at least two months prior
  • HAM-D score of at least 11
  • No history of psychiatric disorders of psychotic features, neurological disorders, or substance abuse in the past 6 months
  • Verified age between 18-65 years old
  • Had no suicidal attempts during the past six months
  • No prior experience with MBCT or other systematic meditation programs

Exclusion Criteria

  • History of psychosis, neurological disorder, and substance abuse for the past 6 months
  • Suicide attempt in past 6 months
  • Prior experience with MBCT or other systematic meditation program

Outcomes

Primary Outcomes

Change from baseline in depressive symptoms as measured by the Hamilton Depression Rating Scale

Time Frame: Once upon recruitment (baseline), and a second time at 8-10 weeks following the MBCT program

Change from baseline in attention regulation, as measured by the Attention Network Test

Time Frame: Once upon recruitment (baseline), and a second time at 8-10 weeks following the MBCT program

Change from baseline in cognitive flexibility, as measured by a computer task involving task-switching and by the Torrance Test for Creative Thinking

Time Frame: Once upon recruitment (baseline), and a second time at 8-10 weeks following the MBCT program

Study Sites (1)

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