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Clinical Trial Summary

Atrial fibrillation is a cardiac arrhythmia commonly encountered in a primary care setting. Current screening is limited to pulse palpation and ECG confirmation when an irregular pulse is found. Paroxysmal atrial fibrillation will, however, still be difficult to pick up. With the advent of smartphones, screening could be more cost-efficient by making use of simple applications, lowering the need for intensive screening to discover (paroxysmal) atrial fibrillation. This cluster randomized trial will examine the effect of using a smartphone-based application such as FibriCheck® on the detection rate of atrial fibrillation in a Flemish general practice population. This study will be conducted in 22 primary care practices across the Flanders region of Belgium and will last 12 months. Patients above 65 years of age will be divided in control and intervention groups on the practice level. The control group will be subjected to standard opportunistic screening only, while the intervention group will be prescribed the FibriCheck® app on top of this opportunistic screening. The difference in detection rate between control and intervention groups will be calculated at the end of the study. The investigators will use the online platform INTEGO for pseudonymized data collection and analysis, and risk calculation. Smartphone applications might offer a way to cost-effectively screen for (paroxysmal) atrial fibrillation in a primary care setting. This could open the door for the update of future screening guidelines.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04545723
Study type Interventional
Source KU Leuven
Contact Tine Proesmans, MSc
Phone +32476856148
Email tine.proesmans@fibricheck.com
Status Not yet recruiting
Phase N/A
Start date January 2024
Completion date March 2024

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