This is a trial to assess the effectiveness of an atrial fibrillation (AF) risk prediction algorithm and diagnostic test for the identification of patients with atrial fibrillation
Study Type
OBSERVATIONAL
Enrollment
260
Local Institution
Ludlow, United Kingdom
Local Institution
Royal Leamington Spa, United Kingdom
Local Institution
Shropshire, United Kingdom
Local Institution
Warkwickshire, United Kingdom
Percentage of participants with diagnosed Atrial Fibrillation during the research window in control and intervention arms
Prevalence of AF in the research window assessed
Time frame: From the first collection of patient medical records at the beginning of the trial to the last collection of patient records following the intervention at the end of the trial (Up to 6 months)
Expected healthcare resource utilisation (Annual maintenance costs related to health states (informed by the primary endpoint), and daily treatment costs (including monitoring))
Time frame: Up to 6 months
Quality-adjusted life years (QALYs)
Time frame: Up to 6 months
Life years (LYs)
Time frame: Up to 6 months
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Local Institution
Wolverhampton, United Kingdom
Local Institution
Worcester, United Kingdom