Everbeat Ring ECG Clinical Concordance Study

Correlation of Electrocardiographic Signals Acquired by a Finger-worn ECG Sensor With a Standard 12-Lead ECG

This study is a cross-sectional observational study conducted in patients referred for routine ECG, to compare output from the everbeat finger-worn ECG device to standard of care (SOC) 12-lead electrocardiography. No intervention is involved in this study. Patients visiting the study site during the study period will be assessed for eligibility on a convenience basis, and observational data will be recorded on those eligible.

Inclusion Criteria:

• Males or females aged 18 to 90 years.
• Under the care of a board-certified physician and referred for a routine electrocardiogram (ECG)
• Resting heart rate between 50 to 120 beats per minute (BPM).

Exclusion Criteria:

• Inability to wear the everbeat ring.
• Prior history of movement disorders including Parkinson's or benign tremors.
• Prior history of allergic skin reactions to metal including stainless steel.