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New home sleep test could make sleep apnea diagnosis easier

NCT ID NCT07476313

Diagnosis Sponsor: Beacon Biosignals Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only This study
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study checks how well a new home sleep test system called SleepView+ can diagnose moderate to severe obstructive sleep apnea in people ages 12 and older. About 200 participants will first use the device during an overnight lab sleep study to compare results, then try it at home on their own. The goal is to see if the device is accurate and easy to use without a technician's help.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 200 people

The number the study aims to enrol. It can still change while the study runs.

Started

Feb 2026

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adults and children aged 12+ years with suspected OSA

Ages

12 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * ≥ 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) Exclusion Criteria: * 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

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Conditions

The condition(s) this trial relates to.

obstructive sleep apnea syndrome

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Obstructive sleep apnea

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    4 sites. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Redwood Pulmonary Medical Associates

    Redwood City, California, 94062, United States

  • Sleep Insights

    Rochester, New York, 14623, United States

  • Sleep Therapy & Research Center

    San Antonio, Texas, 78229, United States

  • West Region Sleep Center

    Cleveland, Ohio, 44135, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.