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Naked-Eye 3-Dimensional Vision Training for Myopia Control

医学 屈光度 随机对照试验 眼科 折射误差 视网膜脱离 干预(咨询) 视力 视网膜 外科 精神科
作者
Rui Xie,Feng Zhao,Jingyi Yu,Bin Luo,Zhidong Jiang,Xing‐Biao Qiu,Yingpin Cao,Yu-Bin Yang,Kezhe Chen,Yuan Zhang,Xiang Liu,Zhirong Wang,Yingting Zhu,Yehong Zhuo
出处
期刊:JAMA Pediatrics [American Medical Association]
标识
DOI:10.1001/jamapediatrics.2024.0578
摘要

Early onset of myopia increases the risk of high myopia, which can lead to irreversible retinal damage and even loss of central vision.To investigate the efficacy and safety of naked-eye 3-dimensional vision training (NVT) in preventing the progression of myopia in children.This randomized clinical trial was conducted in 3 hospitals from May 25, 2022, to February 24, 2023. Participants were children (aged 6-18 years) who had a diagnosis of myopia with a spherical equivalent refraction of -0.75 to -6.00 diopters (D).Children in the intervention group received 20 minutes of NVT treatment every day, whereas children in the control group lived as usual without vision training.The primary outcome was the change in axial length at 6 months. Spherical equivalent refraction (SER) was included as a secondary outcome.Among 263 participants, 125 (47.5%) were male and 138 (52.5%) were female; the mean (SD) age was 10.3 (1.9) years (range, 6.1-15.6 years). A total of 227 patients (86.3%) completed the 6-month follow-up, including 102 in the intervention group and 125 in the control group. In the intervention group, the changes in axial length and SER at 6 months were 0.18 mm (95% CI, 0.16 to 0.20 mm) and -0.25 D (95% CI, -0.31 to -0.19 D), respectively. In the control group, the changes in axial length and SER at 6 months were 0.23 mm (95% CI, 0.21 to 0.25 mm) and -0.35 D (95% CI, -0.41 to -0.30 D), respectively. The differences in AL and SER between the 2 groups were significant (AL difference: -0.06 mm; 95% CI, -0.09 to -0.03; P < .001; SER difference: 0.10 D; 95% CI, 0.02 to 0.19; P = .02). No study-related adverse reactions were reported during follow-up.NVT is a safe and promising means to control myopia progression in children with good adherence.ClinicalTrials.gov Identifier: NCT05468775.
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