- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00623454
Non Cardiac Chest Pain and Benign Palpitations
A Randomized Controlled Trial of Cognitive Behavioural Therapy for Non-cardiac Chest Pain and Palpitations.
All Patients between 18 and 65 years are asked 6 month after investigation for chest pain or palpitation at Cardiological Out-patient Clinic, Molde Hospital, about if they still have symptoms of chest pain or palpitation. If they still have some of the symptoms they are invited to participate in a coping course to learn a better way to deal with their symptoms.
The coping course consist of three sessions of cognitive behaviour therapy.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Phase 4
Contacts and Locations
Study Locations
-
-
-
Molde, Norway, 6400
- Cardiological Out-patient Clinic
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- investigated for chest pain or palpitation 6 month ago at Cardiological Out-patient Clinic, Molde Hospital
- suffer of chest pain or palpitations
Exclusion Criteria:
- do not speak norwegian properly
- mentally retarded
- psychosis last 6 month
- current alcohol or drug misuse
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Body sensation questionnaire (BSQ)
Time Frame: end of treatment, after 3 month and after 12 month
|
end of treatment, after 3 month and after 12 month
|
|
Beck Depression Inventory (BDI)
Time Frame: end of treatment, after 3 and 12 months
|
end of treatment, after 3 and 12 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Egil Jonsbu, MD, Norwegian University of Science and Technology
Publications and helpful links
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
- 4.2006.1110 (REK)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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