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Educational ProblemsNCT05940103

Augmented Reality (AR) Hong Kong

A study testing Augmented Reality (AR) in people with Educational Problems, run by Stanford University at 2 sites in 2 countries.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

This is an international, collaborative study evaluating the non-technical skills (NTS) of anesthesiology residents. The goal is to explore the capability of performing a remote, international AR simulation for the purpose of assessing PALS during a medical crisis. Read more about this study

Who is it for?
Ages 18 to 99 years
Conditions the study is for
Educational Problems
What is being tested?
Augmented Reality (AR)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
0 participants
Where
2 sitesin 2 countries
Study dates
1 Nov 2025to 31 Jul 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 99 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • age above 18

Who cannot join

  • a history of severe motion sickness
  • currently have nausea, a history of seizures
  • wear corrective glasses (they are not compatible with the AR hardware).

Trial locations and contacts

2 sites in 2 countries.

2 sites in 2 countries

United States1 site
  • Lucile Parkard Children's Hospital

    Stanford, California, 94304

Other trials in United States

Hong Kong1 site
  • Queen Mary Hospital

    Hong Kong

Other trials in Hong Kong

About this study

Official title: International Training of Non-Technical Medical Crisis Skills Using Remote, Augmented Reality Simulation

This is an international, collaborative study evaluating the non-technical skills (NTS) of anesthesiology residents. The goal is to explore the capability of performing a remote, international AR simulation for the purpose of assessing PALS during a medical crisis. Simulation experts in the United States will facilitate the AR simulations with anesthesiology residents in Hong Kong. The medical simulation itself is grounded in traditional best practices in accordance with the American Heart Association.

Being tested
Augmented Reality (AR)

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Augmented Reality (AR)Other

    AR headset - a device that the participants will wear over their head and eyes and will add holographic elements to a live view of workplace training scenario

Study groups in NCT05940103
Study groupRoleWhat they receive
Mixed Reality SimulationExperimentalParticipants in the experimental arm will be introduced to workplace training modules through an Augmented Reality (AR) headset.
Receives: Other: Augmented Reality (AR)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Individual performance of non-technical skills assessed by Anaesthetist Non-Technical Skills (ANTS)

    The Anaesthetist Non-Technical Skills (ANTS) scoring system uses four categories assessing task management, teamworking, situation awareness and decision-making (1 to 4 points by categories). The minimum score is 4 and the maximum 16

    Measured: immediately after simulation

Secondary outcomes (3)
  1. Individual performance of non-technical skills assessed by Behaviorally Anchored Rating Scale (BARS)

    The BARS scoring system uses four categories assessing situation awareness, decision-making, communication and teamwork. The score ranges from 1 and 9 (1 = poor and 9 = excellent)

    Measured: immediately after simulation

  2. System Usability Scale (SUS) Score

    The scale has 10 items. Scores ranges from 1-5 (1 = strongly disagree and 5 = strongly agree)

    Measured: immediately after simulation

  3. The International Organization for Standardization (ISO) Ergonomic scale

    The scale has 6 items. Scores ranges from 1-5 (1 = strongly disagree and 5 = strongly agree)

    Measured: immediately after simulation

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Jul 2023
  2. Study start1 Nov 2025 (estimated)
  3. Primary completion31 Jul 2026 (estimated)
  4. Study completion31 Jul 2026 (estimated)

Why it stopped: The collaborator has no intention to initiate the study at this moment.

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05940103
Sponsor's protocol ID
71248
Status last verified
Apr 2026
First submitted
2 Jul 2023
Last updated
24 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Augmented Reality (AR) in people with Educational Problems, run by Stanford University at 2 sites in 2 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 24 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States, Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Individual performance of non-technical skills assessed by Anaesthetist Non-Technical Skills (ANTS) (time frame: immediately after simulation). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Apr 2026.

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