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Randomized Controlled Trial
. 2009 Oct;116(10):1839-45.
doi: 10.1016/j.ophtha.2009.04.004. Epub 2009 Jul 9.

A randomized, clinical trial evaluating ready-made and custom spectacles delivered via a school-based screening program in China

Affiliations
Randomized Controlled Trial

A randomized, clinical trial evaluating ready-made and custom spectacles delivered via a school-based screening program in China

Yangfa Zeng et al. Ophthalmology. 2009 Oct.

Abstract

Purpose: We sought to evaluate visual performance and satisfaction with ready-made spectacles (RMS) in Chinese school-aged children with uncorrected refractive error.

Design: Randomized, double-blind, clinical trial.

Participants: Junior high school students from urban Guangzhou, China, aged approximately 12 to 15 years with > or =1 diopter (D) of uncorrected spherical equivalent (SE) refractive error. Students were excluded with > or =2.00 D astigmatism, > or =2 D myopic anisometropia, and > or =1 D hyperopic anisometropia and ocular disease affecting vision.

Methods: Refractive error was determined by cycloplegic subjective refraction. Students were randomly assigned to receive RMS or custom spectacles (CS) and assessed after 1 month of use. We required 175 students to complete in each arm to be able to measure a 15% difference in compliance.

Main outcome measures: Compliance with spectacles lens wear, patterns of use, vision, symptoms, and perceived value.

Results: Screening identified 965 of 4607 (20.9%) students with reduced distance vision; 212 of the 965 (22.0%) refused evaluation and 187 of the 965 (20.8%) had <1 D of SE refractive error. Sixty-one (6.3%) were referred for further evaluation and the remaining 495 (51.3%) participated. Social, demographic, and ocular parameters were similar in the 2 groups. Average SE refractive error was -2.57+/-1.31 (mean value +/- standard deviation [SD]). Spectacle vision (Snellen acuity, mean +/- SD) was worse with RMS in the eye with lower SE (20/25(-0.5)+/-0.9 lines vs 20/25(+1)+/-0.7 lines; P = 0.004) and higher SE (20/25(-2)+/-1.2 lines vs 20/25(+1)+/-0.8; P<0.001). There were no differences (P>0.05) in the rate of use (94.3% vs 92.2%), wearing to the 1-month visit (46.9% vs 51.5%), planned use (93.3% vs 93.7%), value (89.5% vs 91.7% "moderate or high value or most valued possession"), or symptoms (blur, 21.1% vs 19.4% [P = 0.8] and other symptoms [P>0.2]).

Conclusions: Although visual acuity was better with CS, no difference was found in acceptability in this population of students with predominantly simple myopic refractive error. This study supports the use of RMS in a school-based refractive services program, saving costs and improving the logistics of service delivery.

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Figures

Figure 1
Figure 1
Flow chart of screening and recruitment at 5 junior high schools and progress through the clinical trial. D = diopter; CS = custom spectacles; RMS = ready-made spectacles; SE = spherical equivalent refractive error.
Figure 2
Figure 2
Visual acuity (VA) with the study spectacles for the eye with lower spherical refractive error and the eye with higher spherical refractive error. LogMar = logarithm of the minimum angle of resolution; RMS = ready-made spectacles; SE = spherical equivalent refractive error.

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