Clinical trial Recruiting at 1 site Observational Ages 18 to 70

Eye movement and visual attention in people with thyroid-associated eye disease

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

Run by Shanghai Changzheng Hospital · NCT07381413 · Data updated 2026-11-12

This project uses non-invasive eye tracking to test whether people with thyroid-associated ophthalmopathy track moving objects and scan faces differently than healthy volunteers.

Quick facts

Study typeObservational
Ages18 Years to 70 Years
SexAll
Enrollment100 (estimated)
SponsorShanghai Changzheng Hospital
Academic / other
Locations1 site (Shanghai)
StatusRecruiting
StartedJanuary 31, 2026
Main results expectedMay 2029
Study endsMay 2029
Registry record updatedFebruary 6, 2026
Trial IDNCT07381413 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18–70 with adequate corrected vision who have TAO or are healthy volunteers, can give informed consent, and can follow on-screen instructions.

Probably not a fit

People with severe visual impairment, neurological or psychiatric disorders, prior eye muscle surgery, or recent use of sedating medications are unlikely to benefit or be eligible.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational project will enroll about 100 participants, including people with thyroid-associated ophthalmopathy (TAO) and healthy volunteers. Participants will sit in front of a screen while non-invasive eye-tracking equipment records gaze patterns as they follow moving targets and view faces. Investigators will measure eye stability, tracking accuracy, and how participants scan facial features to quantify physical and social-visual impacts of TAO. The goal is to produce objective data that could inform future monitoring and treatment strategies.

Why it matters

Potential benefit: If successful, the findings could provide objective measures of eye movement and social-visual changes that help clinicians track disease progression and personalize treatments.

How similar studies have gone: Eye-tracking has been used successfully to characterize gaze and eye-movement patterns in other ocular and neurologic conditions, but its application specifically to TAO is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Aged between 18 and 70 years, inclusive.
* Willing and able to provide written informed consent.
* Best-corrected visual acuity (BCVA) ≥ 1.0 in both eyes, with no history of ocular diseases or thyroid disorders.

Exclusion Criteria:

* Non-TAO Ocular Motility Disorders: History of conditions like myasthenia gravis, cranial nerve palsy, or congenital strabismus.
* Neurological Diseases: Disorders affecting oculomotor control (e.g., Parkinson's, MS, stroke, or brain tumors).
* Significant Visual Impairment: BCVA \< 0.5 due to media opacities or retinopathy, preventing clear visualization of stimuli.
* Prior Ocular Surgery: History of surgeries affecting extraocular muscle mechanics (e.g., strabismus surgery, scleral buckling).
* Psychiatric or Cognitive Disorders: Inability to follow instructions or conditions affecting eye movements (e.g., schizophrenia).
* Medication Interference: Use of drugs affecting reaction time (e.g., sedatives) within 48 hours of testing.

Where it's running

  • Changzheng Hospital
    Shanghai, China
    Recruiting

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.