Augmented Reality Medical Simulation

NCT ID: NCT04376255

Last Updated: 2024-09-05

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

101 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-08-18

Study Completion Date

2024-08-16

Brief Summary

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In order to improve the quality of care we provide to patients, medical trainees need to experience low incident, high mortality events in a safe learning environment. There is a selection bias for predisposing characteristics of health care providers, as most people who have pursued a career in medicine are motivated to learn how to manage medical emergencies. Resources have been traditionally enabled with conventional simulation centers or mobile simulation units. However, these are costly and difficult to access. The purpose of this study is to evaluate a mixed reality alternative to conventional simulation. The need for this is inherent in becoming a medical provider and use of these resources will improve health practices and health services.

Detailed Description

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Conditions

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Educational Problems

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Mixed Reality Simulation

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

Group Type EXPERIMENTAL

Augmented Reality (AR)

Intervention Type 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

Interventions

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Augmented Reality (AR)

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

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Trainees or personnel working and/or volunteering at Lucile Packard Children's Hospital Stanford / Stanford Health Care facilities
* 18 years and older

Exclusion Criteria

* Have a history of severe motion sickness
* Currently have nausea
* History of seizures
* Are clinically unstable
* Currently using corrective glasses (not compatible with AR headset)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Stanford University

OTHER

Sponsor Role lead

Responsible Party

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Thomas Caruso

Clinical Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Lucile Packard Children's Hospital Stanford

Palo Alto, California, United States

Site Status

Countries

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United States

Other Identifiers

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55657

Identifier Type: -

Identifier Source: org_study_id

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