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Recruiting NCT07679048

Measuring How Quickly the Eye Focuses After Sustained Viewing of Close-up Images and Videos

No phase Interventional Distance Viewing Prolonged Near Viewing

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Near viewing first, Distant viewing first.
Who it may be relevant to
Registry conditions: Distance Viewing, Prolonged Near Viewing. Basic parameters: 18 years — 35 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

In this experiment, subjects will view a cross pattern on the screen and be asked to focus their eyes on it. The cross pattern will look like it is moving towards and away from the eye in a back-and-forth motion. As the subjects focus their eyes on the shapes, the investigators will measure the focus of their eyes using a device called a wavefront sensor. This device uses infrared light to measure the optical properties of the eye in real time. Our goal is to find out how well the eye focuses before and after viewing images on a screen up close (25cm). Since many people spend a lot of time looking at a computer screen while at work or at school, it is important to understand how this affects the eye's ability to focus.

Detailed description

In this experiment, subjects will view a Maltese cross pattern on a display through a Badal relay. Subjects will be instructed to accommodate to the pattern while a focus-adjustable lens optically moves the display closer and farther in depth as a sinusoidal function of time. As they do so, the investigators will measure the wavefronts of their eyes using a Shack-Hartmann wavefront sensor. The investigators will measure the gain and phase of the accommodative response of the subjects' eyes. Measurements will be made before and after sustained viewing of images on a computer screen 25cm away.

Interventions

  • Other Near viewing first
    In a given session of the experiment (1.5 hours), participants do 2 sets of accommodation tasks. One task happens after viewing a screen for 20 minutes at 25cm, and the other task happens after looking at a distant object (10m) for 20 minutes. In one intervention, the session is structured such that the screen is viewed first ('near viewing first').
  • Other Distant viewing first
    In a given session of the experiment (1.5 hours), participants do 2 sets of accommodation tasks. One task happens after viewing a screen for 20 minutes at 25cm, and the other task happens after looking at a distant object (10m) for 20 minutes. In one intervention, the session is structured such that the distant object is viewed first ('distant viewing first').

Primary outcome measures

  • Gain and phase of ocular accommodation [Time frame: Each measurement takes 10 seconds. In the experiment, the investigators will take measurements over the course of approximately 1 hour.]

Eligibility 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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Crossover
Masking
Open label
Primary purpose
Basic science

Study locations

United States · 1 center
  • Chester F. Carlson Center for Imaging Science — Rochester

Identifiers

NCT: NCT07679048 · IRB0000131-Exp2 · 4R00EY036497-03

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗