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OR black box: could recorded surgeries boost team wellbeing?

NCT ID NCT07396675

Knowledge-focused Sponsor: ORNND - Operating Room Nurse Network Denmark Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jul 24, 2026 · Updated 2 times

Summary

This study tests whether using audio and video recordings from an Operating Room Black Box during team debriefings helps reduce stress and improve teamwork among operating room staff. About 135 healthcare workers from three hospitals will be split into two groups: one using standard debriefings and one using video-assisted debriefings. The goal is to see if the extra data makes debriefings more useful and boosts psychological safety.

What this could mean

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

Active substance
Debriefing (behavioral intervention)
What this could lead to
If successful, this could show that video-assisted debriefings improve teamwork and reduce burnout among operating room staff.
What could go wrong
This is a small, early-stage study (135 participants) comparing two debriefing methods, so results may not apply broadly. The intervention is behavioral, not a treatment, so impact is limited.

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 135 people

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

Started

Mar 2026

Expected to finish

Oct 2027

An estimate. End dates often move.

Lead sponsor

A research network

The lead sponsor is a research network or cooperative group.

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

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Participants work in an OR-team at RIGS, AUMC or UKE. * Participants must have given informed written consent to participate in the study. * Participants must be in the OR for the majority of the procedure or/and have a central role in the teamwork. * At RIGS and AUMC participants for the ORBB debriefings must also be part of teams conducting surgeries in the OR where ORBB is installed (not all ORs have ORBB). * Participants can either be surgeons, anesthesiologist, anesthesia nurses, residents, OR-nurses, perfusionists, interns, nurse students or other OR-staff. Exclusion Criteria: * Visitors, guests, and other staff only watching the surgery, are excluded from participation. * Individuals who are unable or unwilling to provide written informed consent.

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Conditions

The condition(s) this trial relates to.

Burnout, Psychological

As listed by the trial registrant

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

Burnout, healthcare workers Psychological safety Resilience Stress Teamwork

How to take part

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

  1. The places running it

    3 sites in 3 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

  • Amsterdam University Medical Center (Amsterdam UMC)

    NOT_YET_RECRUITING

    Amsterdam, Netherlands

  • Copenhagen University Hospital, Denmark

    RECRUITING

    Copenhagen, 2100, Denmark

  • University Hospital UKE

    NOT_YET_RECRUITING

    Hamburg, Germany

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