WHOOP Abnormal Rhythm Notification

CompletedOBSERVATIONAL
Enrollment

653

Participants

Timeline

Start Date

April 10, 2023

Primary Completion Date

January 25, 2024

Study Completion Date

January 25, 2024

Conditions
Atrial Fibrillation
Interventions
DEVICE

WHOOP 4.0 Strap

Subjects will receive both the WHOOP 4.0 Strap and the BioTel ePatch and will continuously wear each for one week. Data will be collected and analyzed by the study team upon return of the both devices from the subject.

DEVICE

BioTel ePatch

Subjects will receive both the WHOOP 4.0 Strap and the BioTel ePatch and will continuously wear each for one week. Data will be collected and analyzed by the study team upon return of the both devices from the subject.

Trial Locations (1)

06510

Yale University, New Haven

All Listed Sponsors
collaborator

Whoop Inc.

INDUSTRY

collaborator

ZS Associates, Inc.

UNKNOWN

lead

Yale University

OTHER