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Clinical Trials/NCT04376255
NCT04376255
Enrolling By Invitation
Not Applicable

Augmented Reality Medical Simulation: A Multi-Collaborative Study of Acceptance and Usability

Stanford University1 site in 1 country150 target enrollmentAugust 18, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Educational Problems
Sponsor
Stanford University
Enrollment
150
Locations
1
Primary Endpoint
Qualitative Interview Assessment of Remote Simulations
Status
Enrolling By Invitation
Last Updated
2 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
August 18, 2020
End Date
August 18, 2025
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Thomas Caruso

Clinical Associate Professor

Stanford University

Eligibility Criteria

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)

Outcomes

Primary Outcomes

Qualitative Interview Assessment of Remote Simulations

Time Frame: Post-Simulation, Approximate time duration (3-5 minutes)

Primary Aim: The primary aim is to study the acceptance of AR simulation among anesthesia residents using the Technology Acceptance Model (TAM)

Secondary Outcomes

  • System Usability Scale (SUS) Questionnaire(Post-Simulation, Approximate time duration (3-5 minutes))
  • Ergonomic Survey(Post-Simulation, Approximate time duration (3-5 minutes))

Study Sites (1)

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