A Digital Non-interventional Atrial Fibrillation (AF) Screening Study With Commercial Pulse Detection Systems

CompletedOBSERVATIONAL
Enrollment

165

Participants

Timeline

Start Date

November 8, 2017

Primary Completion Date

April 5, 2019

Study Completion Date

May 8, 2019

Conditions
Atrial Fibrillation
Interventions
DEVICE

12-point-ECG

routine recording will be 300 seconds

DEVICE

Polar V800

routine recording will be 300 seconds

DEVICE

360° eMotion FAROS SET + Belt

routine recording will be 300 seconds

DEVICE

Adidas Micoach smart run

routine recording will be 300 seconds

DEVICE

TomTom Runner Cardio HRM

routine recording will be 300 seconds

Trial Locations (1)

Unknown

Many Locations, Multiple Locations

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY