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Smart mattress could replace hospital sleep tests for apnea

NCT ID NCT07432919

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 This study
Registered, but not yet taking participants.
By invitation only
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 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

About 500 people

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

Expected to start

Nov 2026

An estimate. Start dates often move.

Expected to finish

Mar 2028

An estimate. End dates often move.

Lead sponsor

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

Children (under 18), adults (18 to 64) and older adults (65 and over)

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: * 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.

  1. The places running it

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

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    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

  • Center for Biomedical Research of La Rioja

    Logroño, La Rioja, 26006, Spain

  • San Pedro University Hospital

    Logroño, La Rioja, 26006, Spain

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