Diagnostic Accuracy in the Detection of Arrhythmias of Patient Recorded ECGs With Smart WATCH TIMEly Performed During Palpitations

RecruitingOBSERVATIONAL
Enrollment

100

Participants

Timeline

Start Date

February 1, 2024

Primary Completion Date

April 1, 2025

Study Completion Date

October 1, 2025

Conditions
Arrhythmia
Interventions
DIAGNOSTIC_TEST

Recording EKG traces on the smartwatch

Upon enrollment, patients are associated with a progressive identification number (ID). They will then be instructed to record a baseline single-lead EKG (EKG 0) to be sent to a dedicated email address. The sender's email address will be recorded and associated with the ID. The main clinical and demographic data will also be collected. Within 30 days of the enlistment date, a 24-hour EKG Holter will be performed. From the date of enlistment and for the following three months, before, after and during the execution of the 24-hour EKG Holter, enrolled patients can send single-lead EKGs (recorder throug the smartwatch) in case of palpitation. The report of the single-lead EKGs will be communicated electively via e-mail (in response to the email sent by the patient and containing the trace in question) in the following days. In case of diagnostic and/or therapeutic measures to be implemented following the reporting of the trace, doctors will take care of it.

Trial Locations (1)

44124

RECRUITING

Azienda Ospedaliero-Universitaria di Ferrara, Ferrara

All Listed Sponsors
lead

University Hospital of Ferrara

OTHER