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Can augmented reality coach better CPR than a human?

NCT ID NCT07778823

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 21, 2026 · Last updated Aug 27, 2026 · Updated 2 times

Summary

This trial tests whether an augmented reality (AR) system can help healthcare providers deliver high-quality chest compressions during a simulated pediatric cardiac arrest. Participants, who are nurses or technicians with pediatric life support certification, will perform CPR for 18 minutes while receiving real-time visual feedback from the AR-CPR device or coaching from a human instructor. The study aims to see if the AR system is at least as good as human coaching in helping providers meet guideline targets for compression rate and depth.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
AR-CPR, an augmented reality feedback system that provides real-time visual guidance on chest compression rate, depth, and recoil during CPR
What this could lead to
If effective, this could offer a scalable, consistent way to improve CPR quality during pediatric cardiac arrests, potentially saving more lives.
What could go wrong
This is a simulation-based study, so results may not translate directly to real-world emergencies. The technology may also be less effective than human coaching or could have technical issues.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 252 people

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

Started

Jun 2025

Expected to finish

Jun 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.

Ages

18 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: * Actively credentialed pediatric emergency department or pediatric intensive care unit nurse or clinical technician at a participating study site * Current American Heart Association (AHA) Pediatric Advanced Life Support (PALS) certification Exclusion Criteria: * Inability to physically perform chest compressions * Need for prescription corrective lenses without having those corrective lenses available at the time of study participation

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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

    8 sites in 2 countries. 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

  • All Childrens Hopsital

    RECRUITING

    St. Petersburg, Florida, 33701, United States

  • Brown/Hasbro Children's Hospital

    RECRUITING

    Providence, Rhode Island, 02903, United States

  • Childrens Hospital of Philadelphia

    RECRUITING

    Philadelphia, Pennsylvania, 19104, United States

  • Columbia University Vagelos College of Physicians and Surgeons

    RECRUITING

    New York, New York, 10032, United States

  • Johns Hopkins Children's Center

    RECRUITING

    Baltimore, Maryland, 21287, United States

  • Texas Childrens

    RECRUITING

    Houston, Texas, 77030, United States

  • The hospital for sick children

    RECRUITING

    Toronto, Ontario, Canada

  • University of Texas Southwestern Medical center/ Children's Health of Dallas

    RECRUITING

    Dallas, Texas, 75235, United States

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