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Oura Ring OA15 Validation
RecruitingObservational studyHealthy volunteers welcome
Oura Ring OA15 Overnight Features Validation
Who can join
Ages 18 to 85 · All sexes · Healthy volunteers welcome
Full eligibility criteria
Healthy sample Inclusion Criteria: * Ages 18-85 y * Body mass index (BMI) \<30 kg/m2 * Self-reported habitual sleep duration of 6-9 hours * Willing and able to comply with the study requirements Exclusion Criteria: * High risk for mild-to-severe sleep apnea * Individuals with pacemakers * Non-English speakers * Individuals who are unwilling or unable to provide informed consent or comply with study procedures * Current active illness (e.g., cold, flu, bronchitis, suspected COVID-19) * Have known allergies or previous reaction to titanium or medical-grade plastic * Report regularly sleeping \<4 hours per night * Restricted peripheral circulation (e.g. Raynaud's disease) * Individuals with physical limitations or deformities or skin conditions that would preclude safely wearing up to two Oura Ring devices or reference polysomnography equipment * Individuals that have completed overnight rotating shift-work in the past 2 weeks * Individuals that have traveled across time-zones in the past week * Current use (within the past month) of the following medications/classes, pending investigator decision: Stimulants (Adderall, Ritalin); Sodium oxybate; Heroin, cocaine, or methamphetamines; Non-stimulant wake promoting agents (e.g. modafinil, pitolisant, etc.); Prescription sleep medication * Individuals employed by a company that develops or sells medical and/or fitness devices in a similar space (e.g. wearables) or are technology journalists (e.g. professional bloggers, TV, magazine, newspaper reporters, etc.) Sleep Apnea sample Inclusion Criteria * High risk for mild-to-severe sleep apnea, defined by at least one of the following: * Prior clinical diagnosis of obstructive sleep apnea (OSA) * Currently seeking or actively undergoing treatment for sleep apnea (e.g., PAP therapy, oral appliance) * Documented apnea-hypopnea index (AHI) ≥5 events/hour from a previous sleep study * Self-reported Habitual sleep duration of 6-9 hours * Willing and able to comply with study requirements Exclusion criteria * Same as for Healthy Adult sample, with the exception of the "high risk for mild-to-moderate sleep apnea) criterion
About the study
The current study intends to collect data from Oura Ring time-locked to ground truth medical sleep diagnostic gold-standard polysomnography (PSG) for product research and development, investigational algorithm validation, and scientific dissemination.
Sponsor: Ouraring Inc. · Participants: 60 · Started: Aug 28, 2026
Contact the study team
- Emma H Beisheim-Ryan, PT, DPT, PhD · Phone: 585-975-9644
Official record on ClinicalTrials.gov — NCT07908199
Locations in the U.S.
| Missouri | Clayton Sleep Institute Sleep Center, St Louis |
Conditions
From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.