Determining the Validity and Accuracy of Sleep Tracking Using Clinical and Commercially Available Tracking Devices

Overview

About this study

The purpose of this study is to determine which commercially-available tracking devices work best when tracking sleep over seven days, and to investigate the use of heart rate variability when determining sleep quality.

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:

• Healthy men and women between the ages of 18 and 75 will be recruited for this research study.

• No known diagnosis of sleep disorder (e.g. sleep apnea, insomnia, or narcolepsy).

• No known sleep medications (prescription or over the counter).

• A score less than 5 on the Pittsburgh Sleep Quality Index (PSQI).

• Ability to understand study procedures and to comply with them for the entire length of the study.

 

Exclusion Criteria:

• Diagnosis of sleep disorder (e.g. sleep apnea, insomnia, narcolepsy) 

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

Philip Hagen, M.D.

Closed for enrollment

Contact information:

Daniel Gaz

(507)284-7393

Gaz.Daniel@mayo.edu

More information

Publications

Publications are currently not available