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NOT YET RECRUITING
NCT07121816
NA

Use of the ECG Watch in Palpitation Assessment: Feasibility Study

Sponsor: University Hospital, Clermont-Ferrand

View on ClinicalTrials.gov

Summary

Palpitations are the cause of 16% of reasons for consultation with the general practitioner. 41% of palpitations are secondary to cardiac arrhythmia. If a rhythm or conduction disorder is recorded in a symptomatic context, then the cardiac origin can be validated or invalidated. The challenge therefore consists of obtaining an ECG trace during an attack of palpitations (per-critical ECG). Since patients are rarely symptomatic during consultations, additional exploration by ambulatory electrocardiographic recording is essential. To date, the 24-hour Holter ECG is currently the most used in current practice, only has a sensitivity of 22 to 35% maximum depending on the studies. We hypothesize that the ECG watch is a reliable medical tool in the etiological assessment of palpitations, with at least 90% of traces interpretable. The main objective of this study is to validate the use of the ScanWatch watch (Withings®) in the assessment of palpitations.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

120

Start Date

2025-09-01

Completion Date

2028-09-01

Last Updated

2025-08-14

Healthy Volunteers

No

Conditions

Interventions

DEVICE

ECG watch

ECG watch in palpitation assessment

Locations (1)

CHU Clermont-Ferrand

Clermont-Ferrand, France