Clinical trial Recruiting at 1 site Interventional Ages 18 to 35

What your eyes do when you focus after looking at close-up images

Official title: A Randomized, Repeated-measures Study to Measure the Temporal Frequency Response of Ocular Accommodation After Sustained Near Viewing.

Run by Rochester Institute of Technology · NCT07679048 · Data updated 2026-11-12

The study tests how quickly and accurately the eye focuses before and after looking at a computer screen up close in young adults.

Quick facts

Study typeInterventional
Ages18 Years to 35 Years
SexAll
Enrollment20 (estimated)
SponsorRochester Institute of Technology
Academic / other
Locations1 site (Rochester, New York)
StatusRecruiting
StartedJune 25, 2026
Main results expectedDecember 15, 2026
Study endsDecember 15, 2026
Registry record updatedJuly 8, 2026
Trial IDNCT07679048 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18-35 with normal or corrected-to-normal vision.

Probably not a fit

People with vision worse than 20/20 with correction, or conditions prohibiting stable head positioning, may not benefit.

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

What this trial studies

Participants will view a moving Maltese cross while the display changes distance in a controlled way, and eye focus will be measured in real time with a Shack-Hartmann wavefront sensor. The test compares accommodative responses before and after sustained near viewing (25 cm) to see how close-up viewing affects focusing ability. The study uses a Badal relay to adjust image depth while tracking the eye’s optical properties. Normal or corrected-to-normal vision adults aged 18-35 are eligible, and measurements are performed while the head is stabilized. The goal is to better understand short-term changes in accommodation related to near tasks like computer work.

Why it matters

Potential benefit: If successful, the findings could inform guidelines for near-work tasks and eye care to maintain comfortable and accurate focusing.

How similar studies have gone: Prior research has used wavefront sensing to study accommodation, but this specific pre/post near-view protocol is a targeted investigation.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Between 18-35 years of age
* Normal or corrected-to-normal (glasses/contact lenses) vision.

Exclusion Criteria:

* Vision worse than 20/20 while wearing glasses / contact lenses.
* Fragile or loose teeth (participants need to bite a piece of dental clay to stabilize their heads so that measurements can be taken from their eyes)
* Current pregnancy (experiment requires sitting down without moving for stretches of time)
* Heart disease
* Personal/familial history of epilepsy

Where it's running

  • Chester F. Carlson Center for Imaging Science
    Rochester, New York, United States
    Recruiting

Study contacts

  • Principal investigator: Benjamin M Chin, Doctorate — Rochester Institute of Technology
  • Study coordinator: Benjamin M Chin, Doctorate
  • Email: bmccis@rit.edu
  • Phone: 8454534320

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • Longitudinal Visual Diet in Children

    This study follows children ages 7–12 to see how everyday visual factors like distance, light, and viewing patterns relate to myopia development over time.

    Recruiting State University of New York College of Optometry · New York, New York · NCT07642999

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.