Smart mattress could replace hospital sleep tests for apnea
NCT ID NCT07432919
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study will test whether a smart mattress with built-in sensors can accurately diagnose obstructive sleep apnea (OSA) compared to the standard hospital sleep test (polysomnography). Researchers plan to enroll 500 people and have them sleep on the mattress while also undergoing the standard test. If the mattress proves reliable, it could offer a more comfortable, home-friendly way to diagnose sleep apnea and monitor sleep quality.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- smart mattress with sensors
- What this could lead to
- If successful, this could provide a comfortable, non-invasive way to diagnose sleep apnea at home, reducing the need for overnight hospital stays.
- What could go wrong
- This is an early-stage observational study comparing the mattress to standard tests. The mattress may not be as accurate, and results may vary by sleep position or age.
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
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About 500 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Nov 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Diagnostic polysomnographies performed at the Sleep Unit of San Pedro Hospital from November 17, 2026 to March 1, 2028.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: * Polysomnographies performed at San Pedro Hospital between November 17, 2026, and March 1, 2028. * Polysomnographies of patients under 16 years of age and polysomnographies performed at San Pedro Hospital on patients over 16 years of age (as separate study groups). Exclusion Criteria: * Poor technical quality of the polysomnography. * Patients with \>50% central apneas or presence of Cheyne-Stokes respiration (CSResp). * Lack of polysomnography analysis and/or mattress data.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Center for Biomedical Research of La Rioja
Logroño, La Rioja, 26006, Spain
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San Pedro University Hospital
Logroño, La Rioja, 26006, Spain
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Other studies related to the condition(s) this trial covers.
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