This is a prospective, school-based randomized controlled trial designed to evaluate auricular acupressure for myopia prevention in non-myopic primary school students with insufficient hyperopic reserve. Enrolled students in grades 1 to 4 will be randomly assigned to either an auricular acupressure intervention or usual daily activities without additional study-related myopia prevention intervention. Outcomes will include changes in axial length and cycloplegic spherical equivalent refraction, incident myopia, intervention adherence, and safety outcomes over 12 months.
Inclusion Criteria:
Exclusion Criteria:
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Participants in the intervention group will receive auricular acupressure for myopia prevention during the 12-month study period. The intervention will be delivered by trained medical personnel according to a standardized protocol.
Participants in the control group will receive standard school-based eye health education and maintain their usual daily activities during the 12-month study period. They will not receive auricular acupressure or other additional study-related myopia prevention intervention.
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School-based Myopia Prevention Trial for Children With Adequate Hyperopic Reserve
Effects of Auricular Point Pressing With Pellets in Children With Insufficient Hyperopia Reserve
The Efficacy and Safety of Periocular Acupoint Stimulation on Myopia Progression in Children