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

Conditions

• Cardiac Arrhythmia

Eligibility Criteria

Sex

ALL

Age

22 Years - N/A

Healthy Volunteers

Not accepted

Interventions

• Frontier X Plus chest-strap ECG device — 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.
• MoMe ARC ambulatory ECG monitor — DEVICE
  The MoMe ARC monitor will be used as the traditional ambulatory ECG comparator and processed according to standard clinical workflows.

Study Details

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.

Key Dates

First listed

Aug 19, 2026

Start date

Aug 31, 2026

Status verified

Aug 2026

Primary completion

Jan 31, 2027

Completion

Jun 30, 2027

Study Design

Enrollment

15 participants (estimated)

Arms

• Arm: Active Adults Undergoing Ambulatory ECG Monitoring
  Participants prescribed clinical ambulatory ECG monitoring will wear the Frontier X Plus chest-strap ECG device simultaneously with the MoMe ARC traditional ambulatory ECG monitor during their prescribed monitoring period and typical daily activities, including exercise.

Primary Outcome Measure

Concordance of Symptomatic Triggered Events Between Frontier X Plus and MoMe ARC [ Time Frame: 24 hours ]

Central Contacts

• Elizabeth Dineen, DO
  904-953-5230
  [email protected]

Locations (3)

Find similar trials in Scottsdale, AZ

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