- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06766539
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
Status
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Tingting Wang, PhD
- Phone Number: +86 13606812800
- Email: wtingting@zju.edu.cn
Study Locations
-
-
Zhejiang
-
Hangzhou, Zhejiang, China
- Recruiting
- 2nd Affiliated Hospital, School of Medicine, Zhejiang University, China
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
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
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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