NCT06766539

Brief Summary

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.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Dec 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2024

Completed
21 days until next milestone

First Submitted

Initial submission to the registry

December 22, 2024

Completed
18 days until next milestone

First Posted

Study publicly available on registry

January 9, 2025

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

January 9, 2025

Status Verified

December 1, 2024

Enrollment Period

11 months

First QC Date

December 22, 2024

Last Update Submit

January 5, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Identify the "hotspots" where anesthesiologists focus their attention within different areas of the anesthesia machines.

    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 Outcomes (2)

  • The percentage of time anesthesiologists' eyes attention.

    1 year

  • Attention of the clinician

    1 year

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

2nd Affiliated Hospital, School of Medicine, Zhejiang University, China

Hangzhou, Zhejiang, China

RECRUITING

Central Study Contacts

Tingting Wang, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 22, 2024

First Posted

January 9, 2025

Study Start

December 1, 2024

Primary Completion

November 1, 2025

Study Completion

December 1, 2025

Last Updated

January 9, 2025

Record last verified: 2024-12

Locations