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Can simulation make surgery safer? small study aims to find out

NCT ID NCT07570134

Knowledge-focused Sponsor: Yonsei University 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 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study will test a simulation-based training program for new surgical residents, anesthesia nurses, and operating room nurses. Participants will go through two 60-minute team training sessions with realistic scenarios and guided discussions. The goal is to see if this training boosts their confidence in teamwork and readiness to work together, which could improve patient safety.

What this could mean

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

Active substance
Simulation-based interprofessional education sessions
What this could lead to
If successful, this could show that simulation training improves teamwork and patient safety in operating rooms.
What could go wrong
This is a very small pilot study (30 people) at one hospital, so results may not apply elsewhere. It only measures short-term changes in confidence, not actual patient outcomes.

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 30 people

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

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Apr 2027

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

19 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: * Adults aged 19 years or older. * Affiliated with Yongin Severance Hospital and meeting one of the following criteria: * Postgraduate year 1-2 surgical resident; * Newly appointed anesthesia nurse practitioner with less than 6 months of experience in the relevant role; * Newly appointed operating room nurse with less than 6 months of operating room experience. * Able to participate in the planned study procedures during the study period. * Able and willing to provide written informed consent. Exclusion Criteria: * Individuals who do not provide written informed consent. * Individuals who are unable to complete the baseline or post-intervention questionnaires. * Individuals whose rotation, leave of absence, resignation, transfer, or work schedule change makes participation in the study procedures infeasible. * Individuals judged by the investigator to be inappropriate for study participation.

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As listed by the trial registrant

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

Interprofessional relations Medical education Patient safety Teamwork

How to take part

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

  1. The places running it

    1 site. 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

  • Yonsei University Yongin Severance Hospital

    Yongin-si, Gyeonggi-do, 16995, South Korea

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