The overall goal of this study is to develop a combined polygenic risk score (PRS) and metabolic risk score (MRS) and determine its impact on selecting community members for CCS. The trial component of this study will compare the use of these scores to motivate people to adhere to therapy, an ongoing challenge for clinicians, by providing feedback in a meaningful form to both the clinicians and the patients.
Patients undergoing a polygenic risk score (PRS), metabolic risk score (MRS) and coronary calcium score (CCS) will be randomized to receive PRS and CCS information and followed for the reduction of risk over 12 months. This information will provide information about how to motivate people to adhere to therapy, by providing feedback in a meaningful form to both the clinicians and the patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Enrollment
1,059
Risk description to patient based on PRS
Risk description to patient based on CCS
Baker Heart and Diabetes Institute
Melbourne, Victoria, Australia
Change in cardiovascular risk in each group
Change in cardiovascular risk (expressed as pooled cohort equation 10-year risk percentage) from baseline to follow-up
Time frame: 12 months
Medication adherence in each group
Proportion of lipid-lowering tablets taken
Time frame: 12 months
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