Continuous Data Collection and Analysis for Stroke Prevention Using a Wearable Sensor

Overview

About this study

The purpose of this study is to determine whether a wristband that detects your pulse can detect your heart rate and rhythm similar to electrocardiograms (ECG).

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  1. Male or female 18 years of age or older with a primary diagnosis of atrial fibrillation
  2. Willing and able to provide informed consent and follow the study protocol
  3. Clinically indicated planned restoration of normal rhythm

Exclusion Criteria:

  1. Unable to provide informed consent
  2. Unable to follow the study protocol
  3. Women who are pregnant
  4. Subjects with implantable devices (only if participating in phase 2-BodyGuardian processes/testing)

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Paul Friedman, M.D.

Open for enrollment

Contact information:

Siva Mulpuru M.D.

(507)255-2504

Mulpuru.Siva@mayo.edu

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

.
CLS-20391193

Mayo Clinic Footer