- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00497185
Mindfulness-based Cognitive Therapy for Patients With Functional Disorders
Mindfulness-based Cognitive Therapy for Patients With Functional Disorders. A Randomized Controlled Trial
The aim of the study is to examine the efficacy of Mindfulness-Based Cognitive Therapy (MBCT) in patients with functional disorders defined as severe Bodily Distress Disorder.
Hypothesis: MBCT can ameliorate the symptoms of FD defined as severe Bodily Distress Disorder and decrease health care utilization beyond the effect of shared care. Patients treated with MBCT will function better physically and socially than patients treated with shared care at 12 months' follow-up.
Study Overview
Status
Intervention / Treatment
Detailed Description
Functional Disorders (FD) are conditions where patients complain of multiple medically unexplained physical symptoms. FD defy the clinical picture of any conventionally defined disease and cannot adequately be supported by clinical or para-clinical findings. The disorders are common in all medical settings, both in primary and secondary care. The conditions range from mild to severe and disabling, they are costly for society due to the patients' high health care use, and the patients' social and functional level is reduced. There is no well-established, effective pharmacological, or psychotherapeutical treatment offer today.
In randomized controlled trials, cognitive behavioural treatment has shown to be effective for selected patient groups suffering from FD. However, only a few trials have been made, especially concerning treatment of the most severe disorders.
Randomized controlled trials on Mindfulness-Based Stress Reduction (MBSR) have shown mitigation of stress, anxiety, and dysphoria in a general population sample and reduction in total mood disturbances and stress symptoms in a medical population sample. Furthermore, RCTs in Mindfulness-Based Cognitive Therapy (MBCT) have demonstrated a 50 % reduction of depression relapse for individuals, who have experienced three or more previous episodes.
We wish to examine the efficacy of MBCT in patients with functional disorders defined as severe Bodily Distress Disorder.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Aarhus C, Denmark, 8000
- Per Fink
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Functional disorder defined as Bodily Distress Disorder, severe
- Moderate to severe impairment
- The disorder's functional component can easily be separated from a coexisting well-defined physical disease
- No lifetime-diagnosis of psychosis, bipolar affective disorder, or depression with psychotic symptoms
- Age 20-50 years
- Patients of Scandinavian origin, who understand, read, write, and speak Danish
Exclusion Criteria:
- No informed consent
- An acute psychiatric disorder demanding other treatment, or if the patient is suicidal
- Abuse of narcotics or alcohol or (non-prescribed) medicine
- Pregnancy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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OTHER: A
Mindfulness-Based Cognitive Therapy
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Mindfulness-based cognitive therapy: A manualized program will be delivered by two instructors who are experienced cognitive therapists in eight weekly 3½-hour group training sessions and one follow-up session after a month involving up to 12 patients with somatoform disorders. The patients must be willing and able to attend and devote up to 1 hour per day for homework. The therapy is compared with a group of controls receiving shared care defined as: Treatment as usual augmented by psychiatric consultation intervention: The patients are offered a psychiatric consultation after the assessment interview. It is the aim to optimise treatment in the present health care system. |
|
NO_INTERVENTION: B
Shared care: Treatment as usual augmented by psychiatric consultation intervention to optimise treatment in the present health care system.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Physical health measured by SF-36 Physical Component Summary
Time Frame: End of treatment, 6 and 12 months' follow-up
|
End of treatment, 6 and 12 months' follow-up
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
1. Social functioning, emotional disorders, coping: Sub-scales from SF-36, WHO-DAS II, CSQ, SCL, Whiteley-7, lifestyle factors, mindfulness scales. 2. Health care use: Data from national registers.
Time Frame: End of treatment, 6 and 12 months' follow-up
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End of treatment, 6 and 12 months' follow-up
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: Per Fink, DMSc, The Research Clinic for Functional Disorders, Aarhus University Hospital
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 200706
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