Cognitive Restructuring |
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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
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Purpose
| 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
Secondary Outcomes: Health status; Quality of life; Coping; Fear
Expected Total Enrollment: 405
Eligibility
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
Belgium
University Hospital Ghent, Ghent, 9000, Belgium
Cees Van Heeringen, MD, PhD, Principal Investigator, University Hospital Ghent
More Information
Website University Hospital Ghent
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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