Augmented Reality (AR) Chile

NCT05906173 | Completed

• 1 other identifier: 70882
• Study Type: interventional
• Target: 36
• Locations: 1 country
• Sites: 1

Brief 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 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.

Conditions

Educational Problems

Outcome Measures

Primary Outcomes (1)

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

  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 Outcomes (3)

• Individual performance of non-technical skills assessed by Behaviorally Anchored Rating Scale (BARS)

  immediately after simulation

• System Usability Scale (SUS) Score

  immediately after simulation

• ISO Ergonomic scale

  immediately after simulation

Study Arms (1)

Mixed Reality Simulation

EXPERIMENTAL

Participants in the experimental arm will be introduced to workplace training modules through an Augmented Reality (AR) headset.

Other: Augmented Reality (AR)

Interventions

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

Mixed Reality Simulation

Eligibility Criteria

• Age: 18 Years - 99 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• age above 18

You may not qualify if:

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

Sponsors & Collaborators

• Stanford University: lead

Study Sites (1)

Lucile Parkard Children's Hospital

Stanford, California, 94304, United States

Location

Study Officials

• Thomas J Caruso, MD,PhD

  Stanford University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: SUPPORTIVE CARE
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Clinical Professor

Study Record Dates

• First Submitted: June 7, 2023
• First Posted: June 15, 2023
• Study Start: August 10, 2024
• Primary Completion: December 30, 2024
• Study Completion: December 30, 2024
• Last Updated: May 13, 2025

Record last verified: 2025-05

Locations

US (1)