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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT01414751 |
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Date of registration:
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05/08/2011 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Influence of Intervention Methodologies on Patient Choice of Therapy
IMPACT |
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Scientific title:
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Interventions for Chronic Diseases: Effect of Patient Values and Effectiveness Information on Patients' Choice of Therapy, Adherence to Therapy and Satisfaction With Therapy |
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Date of first enrolment:
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November 2009 |
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Target sample size:
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248 |
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Recruitment status: |
Active, not recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01414751 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject)
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Phase:
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N/A
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Contacts
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Name:
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Dorte E Jarbol, MD PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Research Unit of General Practice, Institute of Public Health, University of Southern Denmark |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- 40-69 year-olds
- Patients with a measured total-cholesterol of > 4 MMol/Litre
Exclusion Criteria:
- Patients with diabetes
- Patients with known chronic cardiovascular diseases
- Patients who are already being treated with cholesterol lowering therapy
- Patients who are not familiar with the danish language
Age minimum:
40 Years
Age maximum:
69 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Hypercholesterolemia
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Communication
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Intervention(s)
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Behavioral: Prolongation of life
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Behavioral: Absolute risk reduction
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Primary Outcome(s)
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Patient's satisfaction and confidence with the information given.
[Time Frame: Within two weeks after receiving the information and after 3 months.]
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Secondary Outcome(s)
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Influence of effectiveness format on patients' consent or refusal to a therapy offer
[Time Frame: Within the first week after receiving the information and during the following year.]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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