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OpenTrials
Completed

NCT Number: NCT04376255

Augmented Reality Medical Simulation

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Lucile Packard Children's Hospital Stanford

Palo Alto, California, 94303, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

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

Primary outcomes

  1. 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

  1. System Usability Scale (SUS) Questionnaire

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

    The first secondary aim is to evaluate AR simulation usability via the System Usability Scale (SUS) and ISO 9241-400 Assessment of human-ergonomic factors.

  2. Ergonomic Survey

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

    : The final secondary aim will evaluate the ergonomics of the headset via the ISO 9241-400 Assessment of human-ergonomic factors.

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Registry information

Official study title

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

Important dates

Study start
2020
Primary completion
2024
Study completion
2024
First posted
May 6, 2020
Registry last updated
Sep 5, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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