Remote coaching via head-mounted device may boost ultrasound training

NCT ID NCT07686497

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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.
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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 Results may not be published yet.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)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
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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

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Status unknown
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First seen Jul 07, 2026 · Last updated Aug 13, 2026 · Updated 3 times

Summary

This study compares three ways to teach doctors-in-training how to perform eFAST, a quick bedside ultrasound used to check for internal injuries. All participants watch a short instructional video, then perform three exams on a healthy volunteer. Some get no further help, some get real-time audio guidance from a remote expert, and some get guidance through a head-mounted device that lets the expert see what the trainee sees. Blinded experts later rate the quality of the recorded exams. The goal is to see if live remote guidance, especially with a head-mounted device, leads to better and faster exams than video alone.

What this could mean

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

Active substance
Remote guidance via head-mounted device and audio-only tele-mentoring
What this could lead to
If effective, this approach could improve how emergency ultrasound skills are taught remotely, potentially increasing access to quality training.
What could go wrong
This is a small simulation study with 75 participants, not real patients. Results may not translate to actual clinical settings or different training contexts.

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 75 people

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

Expected to start

Aug 2026

An estimate. Start dates often move.

Expected to finish

Jun 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

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: * Age 18 years or older * Resident physician currently in postgraduate training * Completion of the national Basic Course in Abdominal Ultrasound and the Basic Course in Emergency Ultrasound (SGUM) * Sufficient proficiency in English to understand study instructions, questionnaires, and expert guidance * Able and willing to attend an approximately 45-minute study session * Written informed consent Exclusion Criteria: * Physical limitations that impair ultrasound performance (e.g., upper-limb injury, uncorrected severe visual impairment) * Unable to attend the scheduled session * Participation in conflicting educational studies

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As listed by the trial registrant

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

How to take part

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  2. The official record

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Contacts and locations

Locations

  • Balgrist Campus, University Hospital Balgrist

    Zurich, Canton of Zurich, 8008, Switzerland

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