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CPR timer showdown: does switching every minute save more lives?

NCT ID NCT07624851

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether switching the person doing chest compressions every one minute instead of every two minutes improves CPR quality and reduces fatigue. Eighteen healthcare workers performed CPR on a child-sized manikin under both rotation schedules. Researchers measured compression rate, depth, recoil, and self-reported fatigue to see which interval works better.

What this could mean

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

What this could lead to
If shorter rotation intervals improve CPR quality and reduce rescuer fatigue, this could lead to updated CPR guidelines for pediatric emergencies.
What could go wrong
This is a small pilot study with only 18 participants using a manikin, not real patients. Real-world results may differ, and the findings are too preliminary to change practice yet.

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

18 people

The number who actually took part.

Started

Jul 2024

Finished

Sep 2024

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: * Volunteer pediatric residents * Previous cardiopulmonary resuscitation training * Prior clinical cardiopulmonary resuscitation experience * Ability to participate in both simulated pediatric CPR sessions * Written informed consent provided before study participation Exclusion Criteria: * No previous Pediatric Advanced Life Support course attendance * No prior clinical cardiopulmonary resuscitation experience * Currently rotating in the pediatric emergency department or pediatric ward during the study period * Emergency medicine residents * Presence of a chronic medical condition that could affect physical performance during chest compressions

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Conditions

The condition(s) this trial relates to.

Fatigue

As listed by the trial registrant

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

Contacts and locations

Locations

  • Hacettepe University

    Ankara, Ankara, 06230, Turkey (Türkiye)

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