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Atrial Fibrillation Detection Using Garmin Wearable Technology

Conditions
Atrial Fibrillation
Interventions
Device: Garmin Smart Watch
Device: Garmin Chest Band
Registration Number
NCT03566836
Lead Sponsor
University of Kansas Medical Center
Brief Summary

The purpose of this study is to evaluate the feasibility of detecting atrial fibrillation (AF) in patients with AF using a wearable wrist device/smart watch.

Detailed Description

Even though AF is common and associated with increased risk of stroke, quite often it goes undetected until late in the course of the condition. If AF can be detected with simpler tools like a smart watch, it would enable providers to identify patients with AF much earlier in the course of the condition (even before being seen by a physician) and hopefully be able to prevent stroke. This study is being done to identify a technology that can likely identify AF using a smart watch.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
120
Inclusion Criteria
  • All patients with AF scheduled to undergo electrical cardioversion at the University of Kansas Health System
Exclusion Criteria
  • Patients with no detectable PPG
  • Hemodynamically unstable patients
  • Patients who cannot give informed consent
  • Patients with tattoos on the wrists

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
AF DetectionGarmin Smart WatchParticipants will be asked to wear the Garmin smart watch and Garmin chest band. Both are commercially available. The devices will collect information about heart rates before and after a cardioversion procedure.
AF DetectionGarmin Chest BandParticipants will be asked to wear the Garmin smart watch and Garmin chest band. Both are commercially available. The devices will collect information about heart rates before and after a cardioversion procedure.
Primary Outcome Measures
NameTimeMethod
Sensitivity and specificity of Garmin wearable device in detecting AFVisit 1

PPG samples collected from Garmin wearable will be evaluated and calculated by Garmin custom

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Kansas Medical Center

🇺🇸

Kansas City, Kansas, United States

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