Traditional In-Person Vs. Remote AR Clinical Simulation

NCT ID: NCT06326450

Last Updated: 2025-07-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

42 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-06-22

Study Completion Date

2024-08-03

Brief Summary

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This is a non-inferiority, international, controlled trial that aims to evaluate the progression of physicians and residents through an Advanced Cardiac Life Support (ACLS) clinical simulated scenario. The study's primary objective is to compare the performance outcomes between two groups: participants in the traditional in-person simulation and those immersed in the Augmented Reality (AR) scenario

Detailed Description

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Conditions

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Educational Problems

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Experimental: Augmented Reality Enhanced Simulation (Treatment group)

Participants will experience augmented simulations with a holographic mixed-reality setting based on different workplace scenarios such as medical crisis via Augmented Reality (AR) headset.

Group Type EXPERIMENTAL

Augmented Reality simulation

Intervention Type BEHAVIORAL

Augmented simulation of medical crisis scenarios

Traditional In Situ Simulation (Control group)

Participants will experience in-person simulations of different workplace scenarios such as medical error and workplace harassment

Group Type ACTIVE_COMPARATOR

In Person simulation

Intervention Type BEHAVIORAL

In Person simulation of medical crisis scenarios

Interventions

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Augmented Reality simulation

Augmented simulation of medical crisis scenarios

Intervention Type BEHAVIORAL

In Person simulation

In Person simulation of medical crisis scenarios

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Brazilian resident

Exclusion Criteria

* a history of severe motion sickness
* currently have nausea
* a history of seizures
* wear corrective glasses.
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Stanford University

OTHER

Sponsor Role lead

Responsible Party

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Thomas Caruso

Clinical Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Lucile Parkard Children's Hospital

Stanford, California, United States

Site Status

Countries

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United States

Other Identifiers

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74626

Identifier Type: -

Identifier Source: org_study_id

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