Validation and Usability Study of the SleepView+ Home Sleep Testing System for the Evaluation of Moderate to Severe Obstructive Sleep Apnea.
Enrolling by invitation
Conditions studied: Obstructive Sleep Apnea
In brief
The goal of this observational study is to characterize the performance of the SleepView+ home sleep test system for the evaluation of moderate to severe obstructuve sleep apnea (OSA) in adult and pediatric patients (ages 12 and over). This study is being conducted in patients being evaluated for a sleep disorder who are scheduled to undergo an in lab polysomnigraphic study (PSG), enriching for suspected obstructive sleep apnea. This study will involve two phases: A - comparison of SleepView+ detection of apneas and hypopneas to simultaneously collected in lab PSG (validation phase) and B - evaluation of the ability of patients to use the SleepView+ system in their home environment without sleep technologist support (usability phase) Participants will progress from phase A to phase B.
Key facts
- Study ID
- NCT07476313
- Run by
- Beacon Biosignals
- People needed
- 200
- Starts
- 2026-02-15
- Expected to finish
- 2026-12-15
- Last updated by the study team
- 2026-03-17
Who can join
Age: 12 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- ≥ 12 years of age
- Referred to a sleep lab study site with a clinical indication for an overnight PSG (either full-night or split-night PSG/PAP titration sleep study)
You may not qualify if…
- Age <12 yrs
- Participants who cannot read written instructions in English, have significant cognitive impairment or are otherwise unable to provide informed consent
- Concomitant enrollment in another study protocol that may interfere with data acquisition or reliability of measurements
- Known to be pregnant at time of recruitment
- Stroke or myocardial infarction within 6 months sleep study
- Deemed unsuitable for selection by the research team or medical team due to any medical, legal, social, or interpersonal issues, that would either compromise the study or the routine care of patients.
- Any other medical condition considered high risk or that may impact device usage, as determined by the site PI or medical monitor
Where it is running
- Redwood Pulmonary Medical Associates — Redwood City, California, United States
- Sleep Insights — Rochester, New York, United States
- West Region Sleep Center — Cleveland, Ohio, United States
- Sleep Therapy & Research Center — San Antonio, Texas, United States
Full record on ClinicalTrials.gov
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