- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05906173
Augmented Reality (AR) Chile
May 10, 2025 updated by: Thomas Caruso, Stanford University
Successful 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 NTS during a neonatal medical crisis.
Simulation experts in the United States will facilitate the AR simulations with anesthesiology residents in Chile.
The medical simulation itself is grounded in traditional best practices in accordance with the American Heart Association and Neonatal Resuscitation Program.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
36
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
Stanford, California, United States, 94304
- Lucile Parkard Children's Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- age above 18
Exclusion Criteria:
- a history of severe motion sickness
- currently have nausea, a history of seizures
- wear corrective glasses (they are not compatible with the AR hardware).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mixed Reality Simulation
Participants in the experimental arm will be introduced to workplace training modules through an Augmented Reality (AR) headset.
|
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
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Individual performance of non-technical skills assessed by Anaesthetist Non-Technical Skills (ANTS)
Time Frame: immediately after simulation
|
The Anaesthetist Non-Technical Skills (ANTS) tool previously published by Fletcher et al. translated in French.
The 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
|
immediately after simulation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Individual performance of non-technical skills assessed by Behaviorally Anchored Rating Scale (BARS)
Time Frame: immediately after simulation
|
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)
|
immediately after simulation
|
|
System Usability Scale (SUS) Score
Time Frame: immediately after simulation
|
The scale has 10 items.
Scores ranges from 1-5 (1 = strongly disagree and 5 = strongly agree)
|
immediately after simulation
|
|
ISO Ergonomic scale
Time Frame: immediately after simulation
|
The scale has 6 items.
Scores ranges from 1-5 (1 = strongly disagree and 5 = strongly agree)
|
immediately after simulation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Thomas J Caruso, MD,PhD, Stanford University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 10, 2024
Primary Completion (Actual)
December 30, 2024
Study Completion (Actual)
December 30, 2024
Study Registration Dates
First Submitted
June 7, 2023
First Submitted That Met QC Criteria
June 7, 2023
First Posted (Actual)
June 15, 2023
Study Record Updates
Last Update Posted (Actual)
May 13, 2025
Last Update Submitted That Met QC Criteria
May 10, 2025
Last Verified
May 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 70882
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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