RecruitingNCT07772817

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


Sponsor

Mayo Clinic

Enrollment

15 participants

Start Date

Sep 1, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

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.


Eligibility

Min Age: 22 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Frontier X Plus chest-strap ECG device and a medical device called MoMe ARC ambulatory ECG monitor for people with cardiac arrhythmia. The study is currently recruiting participants at 3 locations. People eligible for this study include aged 22 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEFrontier X Plus chest-strap ECG device

The Frontier X Plus is a chest-strap-based wearable ECG device with embedded dry electrodes and a sensor that captures, stores, analyzes, and transmits ECG data through a mobile application and cloud-based platform for subsequent review.

DEVICEMoMe ARC ambulatory ECG monitor

The MoMe ARC monitor will be used as the traditional ambulatory ECG comparator and processed according to standard clinical workflows.


Locations(3)

Mayo Clinic Arizona

Scottsdale, Arizona, United States

Mayo Clinic Florida

Jacksonville, Florida, United States

Mayo Clinic Rochester

Rochester, Minnesota, United States

View Full Details on ClinicalTrials.gov

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NCT07772817


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