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Recruiting

NCT Number: NCT05184660

Smart Eyewear to Automatically Detect Drug Delivery Events

This project is designed as a prospective observational study of medication preparation and delivery using a novel wearable data input device to automate detection of drug delivery events in the anesthesia workspace at University of Washington Medical Center.

Recruiting

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

Detailed Summary: The goal of this study is to devise a high-fidelity system that automatically collects data about anesthesia care, specifically drug preparation and delivery to the patient. We use a novel wearable data input device that collects computer processed images (video only, no audio) to determine details of the preparation and delivery of medications in the operating room. The wearable data input device is used by an anesthesia provider. The device collects computer processed images and in the anesthesia workspace, which will be used to develop machine learning algorithms that can automatically recognize drug administration events in order to automate medical record keeping in this environment.

Procedure: The principle investigator or a study coordinator will review the electronic operating room schedule to screen for potential data collection. The operating room team will be notified of the study the day prior to and day of data collection. The consented anesthesia provider will wear a point of view device to record drug preparation and drug delivery events in the operating room. Video recordings will be edited to remove Protected Health Information (PHI). Edited footage will then be annotated by volunteers on a computer vision learning tool website. The computer processed images will be then used to develop machine learning algorithms that can automatically recognize drug administration events.

Participants: The initial recruitment goal for the study is 10 nurse anesthetists recording 5 days each in the operating room. Nurse anesthetists are recruited as participants through word of mouth. If determined after data analysis that additional data needs to collected, additional anesthesia providers will be consented.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Anesthesia providers (attending anesthesiologist or certified registered nurse anesthetist) who work in an operating room at University of Washington Montlake Medical Center

Exclusion criteria

  • Medical students and anesthesiology residents

Treatment and study plan

Primary outcomes

  1. Operating room footage

    Time frame: 8-10 hours

    Operating room footage of drug preparation and drug delivery events recorded by anesthesia provider using a point-of-view device.

Secondary outcomes

  1. Computer vision toolkit

    Time frame: 8-10 hours

    A computer vision toolkit which can identify syringes and medications in the hand of a provider in near real time.

Study contacts

Contact information is provided by the study sponsor or research team.

Kelly Michaelsen, MD, PhD

CONTACT

[email protected]

7169085411

Sharon T Nguyen, BS

CONTACT

[email protected]

2066188673

Sponsors and collaborators

Lead sponsor

University of Washington

Other

Registry information

Official study title

The Use of a Wearable Data Input Device (Google Glass, Microsoft HoloLens or GoPro Like Camera Mounted to Eyewear) to Collect Drug Delivery Event Data

Important dates

Study start
2021
Primary completion
2026
Study completion
2026
First posted
Jan 11, 2022
Registry last updated
May 8, 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.