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Implementation and Evaluation of "Mindfulness-Based Cognitive Therapy" in a Health Care Region in Flanders - Article


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Cognitive Restructuring


Clinical Trial: Implementation and Evaluation of "Mindfulness-Based Cognitive Therapy" in a Health Care Region in Flanders

Implementation and Evaluation of "Mindfulness-Based Cognitive Therapy" in a Health Care Region in Flanders

This study is not yet open for patient recruitment.
Verified by University Hospital Ghent May 2005

Sponsors and Collaborators: University Hospital Ghent
Ministry of the Flemish Community
Information provided by: University Hospital Ghent
ClinicalTrials.gov Identifier: NCT00259506

Purpose

Research project regarding the possibility to implement and the efficacy of a non-drug, psychotherapeutic intervention (MBCT), within prevention of recidives of depression
Condition Intervention
Depressive Symptoms
 Behavior: Mindfulness-Based Cognitive Therapy

MedlinePlus related topics:  Depression

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study

Official Title: Implementation and Evaluation of "Mindfulness-Based Cognitive Therapy" in a Health Care Region in Flanders: a Randomized Clinical Trial

Further study details as provided by University Hospital Ghent:
Primary Outcomes: Recidives of depression after 12 months
Secondary Outcomes: Health status; Quality of life; Coping; Fear
Expected Total Enrollment:  405

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • Age over 18 years old
  • given informed consent
  • diagnosis of relapsing depression, at least 3 episodes
  • at least 3 depressive episodes in the anamnesis (either primary or secundary)
  • last depressive episode at least 8 weeks ago
  • absence of a present depressive episode
  • history of medicinal treatment
  • baseline assessment with HRSD < 14
  • absence of exclusion criteria

Exclusion Criteria:

  • based on DSM-IV-TR: lifetime mood disorder, chronic depression, dysthymia, currenct drug abuse, obsessive-compulsory disorder, acute psychose, cognitive disorder, pervasive development disorder, risk of suicide
  • Experienced with zen- or vipassane meditation
  • more than 1 hour practice of zen- or vipassane meditation per week during the last 8 weeks
  • other meditation practices except for MBCT during the training
  • more than 1 psychiatric consultation per 3-4 weeks during the training and follow-up
  • intensive psychotherapy during the trainng or follow-up
  • schezonphrenia or schezo-affective disorder in anamnesis
  • physical problems which make it difficult to participate in the programme

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00259506

Karen Godfrin      0032/9/240.58.94    karen.godfrin@ugent.be

Belgium
      University Hospital Ghent, Ghent,  9000,  Belgium
Karen Godfrin  0032/9/240.58.94    karen.godfrin@ugent.be 

Study chairs or principal investigators

Cees Van Heeringen, MD, PhD,  Principal Investigator,  University Hospital Ghent   

More Information

Website University Hospital Ghent

Study ID Numbers:  2005/195
Last Updated:  December 8, 2005
Record first received:  November 28, 2005
ClinicalTrials.gov Identifier:  NCT00259506
Health Authority: Belgium: Institutional Review Board
ClinicalTrials.gov processed this record on 2006-01-10


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August 21, 2008



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