High Blood Pressure, Hypertension
Conditions
Brief summary
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.
Interventions
None listed
Sponsors
Study design
Eligibility
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sensitivity of the Oura Blood Pressure Profile classification for identifying participant-reported hypertension | From enrollment until up to 18 months |
Secondary
| Measure | Time frame |
|---|---|
| Specificity of the Oura Blood Pressure Profile classification versus participant-reported hypertension | From enrollment until up to 18 months |
Countries
United States