Arrhythmia Clinical Trial
Official title:
Assessment of Portable Remote Health Monitor Using the Snap to Symptomatic Arrhythmia
Participants in the Snap arm were instructed to undertake once-day recording and transmission of a 30-second single-lead iECG trace to a secure server, plus additional submissions if symptomatic over a 3-month period. Snap traces were analyzed by an automated analysis software and cardiologists. Clinical review and appropriate care was arranged for those clinically significant arrhythmia. Patients in the RC group were followed up as normal methods including ECG, Holter.
Individuals with symptomatic arrhythmia without known arrhythmia were recruited.
Participants were required to have access to the internet via WiFi and to be able to operate
the Snap system after simple instruction. Written consent was obtained, and eligible
participants were randomized (1:1) to an intervention (Snap) group or RC group.
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