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Recruiting NCT07642999

Longitudinal Measurements of Visual Diet in Children

Conditions: Myopia, Visual Diet, Pupil, Viewing Distance, Illuminance, Wavelength, Vergence, Accommodative Facility

Sex: All
Ages: 7 Years – 12 Years
Healthy volunteers: Yes
Enrollment: 60
Sponsor: State University of New York College of Optometry

Location: SUNY College of Optometry New York New York

Summary

Myopia is a leading cause of visual impairment worldwide, with prevalence rising rapidly among children. Growing evidence suggests that environmental and behavioral factors play a dominant role in ocular growth; however, current studies typically isolate single components of the visual environment, such as near work or light intensity, limiting investigators' understanding of how multiple visual stimuli interact within individuals over time. The retina is continuously exposed to a dynamic "visual diet," encompassing viewing distance, illuminance, spectral composition of light, and temporal viewing patterns, as well as associated visuomotor responses such as eye vergence and pupil dynamics. A critical barrier to myopia prevention is the lack of longitudinal, quantitative measurements that integrate these factors in real-world settings during childhood ocular development. The long-term goal of this project is to prevent myopia onset and slow myopia progression through individualized, patient-centered monitoring and modification of the visual diet. The overall objective of this proposal is to longitudinally characterize visual diet and visuomotor behavior in children and to identify the most influential environmental and physiological factors driving myopia onset and progression. The investigators will conduct a 3-year longitudinal observational study enrolling 60 children aged 7-12 years, including myopic children and non-myopic children stratified by risk of myopia progression.

Eligibility Criteria

Inclusion Criteria: * Age: 7-12 years old (inclusive) * Astigmatism of \< 1.50D * Stereopsis equal or better 100 seconds of arc * Normal binocular functions. In addition, for the Myopic group: \- Cycloplegic autorefraction (spherical equivalent, SEQ) between -0.50D and -6.00D, who are not currently pursuing nor intending to start myopia control at the time of enrollment. For the non-myopic group: \- SEQ between plano and +2.50D. Exclusion Criteria for both groups: * History of refractive surgery or myopia control * Binocular abnormalities * Ocular and systemic pathologies * Developmental delay * Unable to wear the VEET at home for 8 days every 6 months for 3 years * Pre-term birth (\< 34 weeks of gestational age).

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07642999). StuddyBuddy aggregates publicly available trial information.