Multicenter Study of Near Vision Behavior and Outdoor Time in Children Undergoing Myopia Control

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY

Currently, optical and pharmacological interventions have been developed to prevent the progression of childhood myopia. However, no myopia control strategy has been shown to have complete efficacy in controlling myopia progression in children. One possible reason is that risk factors contributing to the development of myopia were not controlled in previous clinical studies including time outdoors and near vision behaviour. This study aims to quantify time spent outdoors and near vision behavior in myopic children and its impact on myopia control efficacy. The outcomes of this study will guide clinicians on risk management and improve responses to existing treatments for progressive myopia.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 4
Maximum Age: 14
Healthy Volunteers: f
View:

• Aged 6 to below 14 years old

• Spherical equivalent myopic refractive error greater than -0.50 D

• Best corrected logMAR visual acuity of 0.1 or better in each eye for 6- to 14-year-old children, and 0.2 logMAR or better than in each eye for 4 and 5-year-old children (adjusted for age-related expectations)

• Good ocular and general health that would not preclude them from myopia control

• Competent enough in English to fully understand the participant information and consent form

• Willing to undergo treatment to slow myopia progression for one year

Locations
United States
California
School of Optometry, University of California, Berkeley
ACTIVE_NOT_RECRUITING
Berkeley
Massachusetts
New England College of Optometry
RECRUITING
Boston
New York
State University of New York (SUNY), College of Optometry
NOT_YET_RECRUITING
New York
Other Locations
Australia
Optometry and Vision Science, Queensland University of Technology
RECRUITING
Kelvin Grove
School of Optometry and Vision Science, UNSW
RECRUITING
Sydney
Contact Information
Primary
Pauline Kang, PhD
p.kang@unsw.edu.au
612 9065 6112
Time Frame
Start Date: 2023-03-21
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 230
Related Therapeutic Areas
Sponsors
Collaborators: University of California, Berkeley, New England College of Optometry, State University of New York College of Optometry, Queensland University of Technology
Leads: The University of New South Wales

This content was sourced from clinicaltrials.gov