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Atrial Fibrillation

Elegibility:

  • Age 22 or older

  • Able to understand and provide informed consent

  • Able to stand still and hold the study device as instructed

  • Willing to participate in study procedures during a single visit

  • Known diagnosis of atrial fibrillation and in AF at the time of screening

Descriptions:
This study is evaluating a noninvasive, connected ECG device designed to help detect atrial fibrillation (AF). Adults will participate in a single study visit where heart rhythm recordings from the study device are compared with a standard 12-lead ECG. The goal of the study is to assess how accurately the device can identify atrial fibrillation and normal heart rhythm. Participation involves brief ECG recordings taken while standing at rest and, for some participants, after light physical activity.

Join Study

Interested in participating in this study? Complete the form below to find out if you qualify. Once we receive your information, a member of our research team will contact you to review your eligibility and provide more details about the study. All information is kept confidential and protected under HIPAA regulations.

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