Auricular Acupressure to Help Prevent Myopia in Young Kids With Limited Hyperopic Reserve
Official title: A Randomized Controlled Trial of School-based Auricular Acupressure for Myopia Prevention in Non-myopic Children With Insufficient Hyperopic Reserve
Run by Shanghai Eye Disease Prevention and Treatment Center · NCT07746804 · Data updated 2026-11-12
This trial tests whether auricular acupressure, added to standard eye health education, can help prevent myopia in elementary students who don’t have enough hyperopic reserve.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 6 Years to 11 Years |
| Sex | All |
| Enrollment | 130 (estimated) |
| Sponsor | Shanghai Eye Disease Prevention and Treatment Center Academic / other |
| Locations | 1 site (Shanghai, Shanghai Municipality) |
| Status | Recruiting |
| Started | June 1, 2026 |
| Main results expected | June 2027 |
| Study ends | December 2027 |
| Registry record updated | August 5, 2026 |
| Trial ID | NCT07746804 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are non-myopic children in grades 1–4 with insufficient hyperopic reserve and with guardian consent.
✕Probably not a fit
Children with normal hyperopic reserve, existing myopia, or conditions preventing auricular acupressure are less likely to benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
In this school-based, randomized study, children in grades 1–4 with insufficient hyperopic reserve and no myopia are assigned to receive auricular acupressure plus eye health education or eye health education alone for 12 months. The primary outcome is change in axial length from baseline to 12 months, with secondary outcomes including changes in cycloplegic refraction, incident myopia, adherence, and safety. Assessments occur at baseline, 6 months, and 12 months through comprehensive eye examinations. The study aims to determine if the auricular acupressure intervention can slow eye growth and help prevent myopia in this at-risk group.
Why it matters
Potential benefit: If successful, the intervention could become a low-burden option to help delay or reduce the onset of myopia in children.
How similar studies have gone: Previous studies have explored non-traditional approaches for myopia prevention, but evidence for auricular acupressure in this setting is limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Students in grades 1 to 4 from participating primary schools. * Non-myopic children with insufficient hyperopic reserve, defined as cycloplegic spherical equivalent refraction in the worse eye greater than +0.75 D and below the following age-specific upper limits: +1.72 D at age 6 years; +1.48 D at age 7 years; +1.19 D at age 8 years; +1.11 D at age 9 years; +0.92 D at age 10 years; and +0.83 D at age 11 years. * Written informed consent provided by a parent or legal guardian, with willingness to participate in baseline and follow-up assessments during the study period. Exclusion Criteria: * Strabismus, amblyopia, or other ocular abnormalities. * Systemic disease or other medical conditions that may affect study participation. * Has received any myopia prevention intervention in the past 3 months. * Known skin sensitivity, local ear skin lesions, or other conditions judged unsuitable for auricular acupressure. * Any other condition judged by the study doctors to make participation inappropriate.
Where it's running
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Shanghai Eye Disease Prevention and Treatment Center
Shanghai, Shanghai Municipality, China Recruiting
Study contacts
- Study coordinator: Xiangui He, PhD
- Email: xianhezi@163.com
- Phone: +86 021-62717733
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.