Feasibility and Usability of a Chest-Strap Ambulatory ECG Monitor in Active Individuals in Comparison With a Traditional Ambulatory ECG Patch Monitor (MoMe ARC)

Feasibility and Usability of a Chest-Strap Ambulatory ECG Monitor in Active Individuals in Comparison With a Traditional Ambulatory ECG Patch Monitor (MoMe ARC)

The purpose of this research is to compare the standard ambulatory ECG monitor, the MoMe ARC, against Fourth Frontier's "Frontier X Plus". This device is an FDA-Cleared chest-strap-based ECG wearable that provides an alternative modality to capture ambulatory ECG rhythm changes.

Inclusion Criteria:

• Adult participants (>22 years; Frontier X is approved for use in this age group) who participate in >4 days a week of >150 minutes total per week of moderate to high intensity exercise who were prescribed a ambulatory ECG monitor for clinical purposes for 24 hours or more.
• Patients must agree to wear the Frontier X monitor for the prescribed duration and use the Frontier X Plus application

Exclusion Criteria:

• Current use of Implanted Cardiac Devices
• Pregnancy
• Known allergies to any of the materials listed in the "List of Patient-Contacting Materials"
• Presence of skin injuries or broken skin in the area where the chest strap is worn
• Inability to use a compatible mobile device required for the operation of the study device
• Any cognitive or physical limitations that, in the opinion of the investigator, limits the participant's ability to fully follow study procedures
• Medical restrictions on exercise for safety including cardiac, orthopedic or other relevant past medical history