Actively Recruiting

Age: 18Years - 70Years
All Genders
Healthy Volunteers
ID07381413

Eye Tracking Study on Eye Movement Function and Visual Attention Patterns in Patients With Thyroid-Associated Ophthalmopathy

Led by Shanghai Changzheng Hospital · Updated on 2026-02-06

100

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating eye health and visual function in people with Thyroid-Associated Ophthalmopathy (TAO), a condition that can cause bulging eyes and limited eye movement. This study aims to use non-invasive eye-tracking technology to measure how TAO affects eye movement and visual attention compared to healthy individuals. The goal is to objectively understand how the disease impacts physical eye function and social behaviors like eye contact. Participants will undergo a single, standardized visit where they will complete a visual function assessment using a desktop high-frequency eye tracker. The test includes calibration to ensure accurate tracking, oculomotor tasks to evaluate eye stability and smooth pursuit ability, and visual attention tasks to record how participants scan static images. This process is non-invasive and takes about 15 to 20 minutes. During the visit, researchers will record gaze patterns and measure outcomes such as smooth pursuit function, central fixation stability, gaze distribution on eye areas, and extraocular muscle thickness. These measures will help quantify the disease's effects. The study will include 100 participants, both patients with TAO and healthy volunteers, aged 18 to 70 years. The entire participation involves this brief assessment without any treatment or further follow-up.

CONDITIONS

Brief Title

Eye Tracking Study on Eye Movement Function and Visual Attention Patterns in Patients With Thyroid-Associated Ophthalmopathy

Who Can Participate

Age: 18Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged between 18 and 70 years, inclusive
  • Willing and able to provide written informed consent
  • Best-corrected visual acuity (BCVA) 21 1.0 in both eyes, with no history of ocular diseases or thyroid disorders
Not Eligible

You will not qualify if you...

  • History of non-TAO ocular motility disorders such as myasthenia gravis, cranial nerve palsy, or congenital strabismus
  • Neurological diseases affecting eye movement control (e.g., Parkinson's, multiple sclerosis, stroke, brain tumors)
  • Significant visual impairment with BCVA < 0.5 due to media opacities or retinopathy
  • Prior ocular surgery affecting extraocular muscle mechanics (e.g., strabismus surgery, scleral buckling)
  • Psychiatric or cognitive disorders affecting ability to follow instructions or eye movements (e.g., schizophrenia)
  • Use of medication affecting reaction time (e.g., sedatives) within 48 hours of testing

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 1 day

Participants undergo a non-invasive eye tracking assessment to evaluate eye movement function and visual attention patterns.

1 study visit lasting approximately 15-20 minutes (in-person)

Trial Site Locations

Total: 1 location

1

Changzheng Hospital

Shanghai, China

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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