Affiliation:
1. State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Guangdong Provincial Key Laboratory of Ophthalmology Visual Science, Guangdong Provincial Clinical Research Center for Ocular Diseases, Sun Yat-sen University, Guangzhou, China
2. Foshan Women and Children‘s Hospital, Foshan, Guangdong, China.
3. Department of Ophthalmology, Shenzhen People‘s Hospital (The Second Clinical Medical College, Jinan University), Shenzhen, Guangdong, China
Abstract
ImportanceEarly onset of myopia increases the risk of high myopia, which can lead to irreversible retinal damage and even loss of central vision.ObjectiveTo investigate the efficacy and safety of naked-eye 3-dimensional vision training (NVT) in preventing the progression of myopia in children.Design, Setting, and ParticipantsThis 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).InterventionChildren in the intervention group received 20 minutes of NVT treatment every day, whereas children in the control group lived as usual without vision training.Main Outcome and MeasureThe primary outcome was the change in axial length at 6 months. Spherical equivalent refraction (SER) was included as a secondary outcome.ResultsAmong 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.Conclusions and RelevanceNVT is a safe and promising means to control myopia progression in children with good adherence.Trial RegistrationClinicalTrials.gov Identifier: NCT05468775
Publisher
American Medical Association (AMA)
Cited by
1 articles.
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