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Purpose

The proposed study is designed as a prospective, single-arm, observational, non-significant risk device study to evaluate the performance of Oura's investigational Blood Pressure Profile algorithm in identifying signs of hypertension.

Conditions

Eligibility

Eligible Ages
Over 22 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Located in United States - Aged 22 years or older at time of eligibility screener - Oura Ring user (Oura Ring Gen3 or newer) - User of the English version of the Oura App - Smartphone (iOS or Android) user - Able to provide consent electronically

Exclusion Criteria

  • User of implanted cardiac electronic device(s) - Currently pregnant - Within 12 weeks postpartum

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Recruiting Locations

Ouraring
San Francisco, California 94108
Contact:
Senior Research Project Manager
bp-profile-study@ouraring.com

More Details

Status
Recruiting
Sponsor
Ouraring Inc.

Study Contact

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.