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Evaluate Sleep Quality from Wearable Physiologic Monitor

Overview

About this study

The purpose of this study is to demonstrate proof-of-concept feasibility for Mayo OMNI physiologic monitor correlation with sleep-wake measures obtained from the current gold-standards of actigraphy and polysomnography. 

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:

  • Adults  > 18 years of age.
  • Body-Mass Index (BMI) < 35.
  • Normal sleep routine (typically awake during day and asleep at night).

Exclusion Criteria: 

  • Prior diagnosis of, or positive STOP-BANG screen (> 3) for sleep apnea.
  • Excessive daytime sleepiness (the recorded Epworth Sleepiness Scale (ESS) must be ≤ 9).
  • History of heart failure, atrial fibrillation, pulmonary, neurological, or psychiatric disease.
  • Currently being treated pharmacologically for depression or other significant medical condition (broadly speaking).
  • Subject is receiving hypnotics or stimulant medication.
  • Habitual use of 3 or more cups of coffee/caffeinated tea per day.

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

Timothy Morgenthaler, M.D.

Closed for enrollment

Contact information:

Michelle Grady CCRP

(507) 284-8903

Grady.Michelle@mayo.edu

More information

Publications

Publications are currently not available

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CLS-20532788

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