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Study of Mindfulness-Based Cognitive Therapy

NCT ID: NCT00943033

Last Updated: 2012-09-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-08-31

Study Completion Date

2010-07-31

Brief Summary

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Research aimed at assessing changes in depressogenic thinking and the ability to disengage from depressogenic thinking following Mindfulness-Based Cognitive Therapy

Detailed Description

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Conditions

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Major Depressive Disorder

Keywords

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MBCT Mindfulness-Based Cognitive Therapy Mindfulness Meditation Relapse Prevention Recurrent Depression Depression Major Depressive Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Mindfulness-Based Cognitive Therapy plus treatment as usual

Group Type EXPERIMENTAL

Mindfulness-Based Cognitive Therapy

Intervention Type BEHAVIORAL

Mindfulness-Based Cognitive Therapy for the prevention of depressive relapse/recurrence

MBCT Waitlist plus Treatment as Usual

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Mindfulness-Based Cognitive Therapy

Mindfulness-Based Cognitive Therapy for the prevention of depressive relapse/recurrence

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* History of two or more Major Depressive Episodes or history of a Major Depressive Episode lasting at least one year
* Can speak, read, and understand English

Exclusion Criteria

* Meet Criteria for Current Major Depressive Episode or are in partial remission
* BDI-II score above 19
* Abuse alcohol or drugs
* Current Dysthymic Disorder
* History of: psychosis when not depressed or intoxicated, Mania, Hypomania, Obsessive Compulsive Disorder, Posttraumatic Stress Disorder, Anorexia Nervosa, Bulimia Nervosa
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Binghamton University

OTHER

Sponsor Role lead

Responsible Party

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Sean Barnes

PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Sean M. Barnes, MS

Role: PRINCIPAL_INVESTIGATOR

Binghamton University SUNY

Other Identifiers

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MLI-FJVRF-08-SMB

Identifier Type: -

Identifier Source: org_study_id