The Application of Eye-Tracking Technology in Perioperative Management and Education

The Application of Eye-Tracking Technology in Perioperative Management and Education: a Prospective Observational Study

The goal of this observational study is to explore the value of eye-tracking technology in perioperative management and teaching. The study aims to understand how eye-tracking can help analyze the attention distribution of clinicians during perioperative procedures and optimize workflows for improved safety and teaching outcomes.

The main questions it seeks to answer are:

How does eye-tracking technology reveal the focus distribution patterns of experienced and novice clinicians in perioperative scenarios? Can visualizing expert clinicians' eye movement patterns improve the learning outcomes and operational skills of medical students?

Participants include anesthesiologists and medical students involved in perioperative management training. Eye-tracking data, such as fixation duration, fixation count, and heatmaps, will be collected during surgical and training scenarios. The study will analyze correlations between attention distribution and operational performance. This research will provide insights into optimizing perioperative safety and revolutionizing medical education using objective attention data.

Study Overview

Study Type

Observational

Enrollment (Estimated)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Zhejiang
      • Hangzhou, Zhejiang, China
        • Recruiting
        • 2nd Affiliated Hospital, School of Medicine, Zhejiang University, China

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Anesthesiologists, including senior physicians and junior doctors and medical students undergoing perioperative management training.

Description

Inclusion Criteria:

  • Anesthesiologists, including senior physicians and junior doctors.
  • Medical students undergoing perioperative management training.

Exclusion Criteria:

  • Individuals with ophthalmological conditions that affect eye movement function.
  • Participants who fail to complete the full experimental protocol.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Identify the "hotspots" where anesthesiologists focus their attention within different areas of the anesthesia machines.
Time Frame: 1 year

Every anesthesiologist will record data from three cases. Data collection will commence as the general anesthesia procedure begins when the patient moves onto the surgical table and will complete when the patient reaches the states of sedation and unconsciousness in preparation for the operation. This period, during which the anesthesiologist plays a leading role, typically lasts less than 10 minutes. No data will be recorded once the surgical operation begins.

The Tobii eye-tracker will generate a diverse dataset, encompassing eye trajectory, fixation (a gaze resting on a spot for more than 150 ms), saccades (rapid eye movements between two distinct points), and pupil size. This comprehensive dataset enables us to identify the "hotspots" where anesthesiologists focus their attention within different areas of the anesthesia machines.

1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The percentage of time anesthesiologists' eyes attention.
Time Frame: 1 year
Moreover, we will calculate the percentage of time anesthesiologists' eyes spend on team members. We will also quantify the duration of eye contact and communication content between the anesthesiologist and each team member.
1 year
Attention of the clinician
Time Frame: 1 year
Finally, we will examine the correlation between these behavioral measures (e.g., fixation on hotspots, percentage of time focused on team members, communication episodes) and the duration of the anesthesia procedure.
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2024

Primary Completion (Estimated)

November 1, 2025

Study Completion (Estimated)

December 1, 2025

Study Registration Dates

First Submitted

December 22, 2024

First Submitted That Met QC Criteria

January 5, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 5, 2025

Last Verified

December 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 2024-1282

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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