Eye Tracking in Laryngology

Sponsor
Mayo Clinic (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05034575
Collaborator
(none)
120
1
1
29.1
4.1

Study Details

Study Description

Brief Summary

The purpose of this study is to assess whether eye-tracking technology can be used to differentiate the visual gaze patterns of experienced and novice laryngoscopists while reviewing prerecorded laryngeal videos with both normal and abnormal findings and to characterize any differences arising between level of training groups.

Condition or Disease Intervention/Treatment Phase
  • Other: Eye Tracking Technology Sensor
N/A

Detailed Description

Novice and experienced participants will be recruited to take part in this study. Novices include medical students without practical experience in otorhinolaryngology and resident physicians at different stages in training. Trainees, residents and experts from fields of gastroenterology and pulmonology will also be included. The experienced group will be defined as consultants and speech pathologists.

This study will look at multiple areas within otolaryngology including laryngology, rhinology, facial plastic surgery, head and neck oncology, and otology. Participants will view prerecorded videos and/or still pictures absent of patient identifiers.

There will be two tasks each taking approximately 10 minutes. Task order will be alternated between subjects with one task asking participants to view 7 still images from video laryngoscopy examinations. After each image participants will rate how likely the image is to represent glottic cancer and what portion of the image they deemed most important to their decision. For the second task, participants will be asked to view a 5 second video of a flexible laryngoscope exam, after which, they will be asked to identify the presence and side of vocal fold paralysis as well as note the location they deemed most important to their decision.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
A Study to Assess Eye Tracking and Visual Gaze Patterns in Laryngology
Actual Study Start Date :
Jun 29, 2021
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Novice and experienced medical personnel

Participants will be asked to complete two tasks each taking approximately 10 minutes while wearing eye-tracking technology to understand focus of gaze during laryngeal endoscopy and stroboscopy interpretation.

Other: Eye Tracking Technology Sensor
Eye tracking will be performed using Tobii Pro eye tracking technology sensor (Tobii Pro Fusion, Stockholm, Sweden), providing binocular eye tracking up to 250 Hz. The sensor, positioned on the inferior aspect of the computer monitor, reflects infrared (IR) light beams off of each cornea and are subsequently captured.

Outcome Measures

Primary Outcome Measures

  1. Time to Fixation Fixation Point [15 minutes]

    Defined as the temporary suspension of eye movement (80ms) on a specific point (≤ 30 pixels) within the field of view.

  2. Percent of Fixation Time on pre determined area of interest [15 minutes]

    Defined as the percent of total gaze time on area of interest

  3. Count of Fixations [15 minutes]

    Number of times observer returns gaze to area of interest

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Adults, age 18 and over.

  • Already professionals in a laryngology related field, residents in a related field or students considering a related field.

  • Related fields include otolaryngology, laryngology, and speech language pathology.

Exclusion Criteria:
  • Anyone not meeting the inclusion criteria or anyone not wishing to participate.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic in Rochester Rochester Minnesota United States 55905

Sponsors and Collaborators

  • Mayo Clinic

Investigators

  • Principal Investigator: Diana Orbelo, PhD, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Diana M. Orbelo, Principal Investigator, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT05034575
Other Study ID Numbers:
  • 20-012365
First Posted:
Sep 5, 2021
Last Update Posted:
Sep 5, 2021
Last Verified:
Aug 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Sep 5, 2021