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A prospective cohort study on the correlation between eye-use behavior and myopia in children based on Eye-Monitor

A prospective cohort study on the correlation between eye-use behavior and myopia in children based on Eye-Monitor

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102788
Enrollment
Unknown
Registered
2025-05-20
Start date
2022-10-31
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myopia

Interventions

Sponsors

Affiliated Eye Hospital of Shandong University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
7 Years to 9 Years

Inclusion criteria

Inclusion criteria: 1. All children in grades 2-3; 2. The astigmatism in both eyes is = 1.0; 4. No organic lesions are diagnosed based on clinical or laboratory evidence; 5. The intensity and environment of the children's eye use are similar; 6. Participants voluntarily sign informed consent forms.

Exclusion criteria

Exclusion criteria: 1. Individuals with organic lesions such as corneal, iris, lens, and fundus lesions that affect vision in both or one eye, as well as subjects with amblyopia; 2. Children under myopia-control treatments are excluded within 3 months prior to the start of the project, including Long term use of traditional Chinese medicine external treatment methods (including acupuncture, electroacupuncture, tuina, moxibustion, ear acupressure, etc.), orthokeratology, rigid gas permeable contact lens, progressive multifocal spectacles, peripheral defocus spectacles, multifocal and defocus soft contact lenses, low concentration atropine eye drops, visual therapy and other related treatments that have not been terminated; 3. Individuals with severe systemic diseases, such as cardiovascular, cerebrovascular, liver, kidney, hematopoietic system, and mental disorders; 4. Individuals with communication disorders and mental illness; 5. Individuals participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
The changes in spherical equivalent of right eye;

Secondary

MeasureTime frame
The changes in axial length of right eye;The percentage of children with newly developed myopia of right eye;Fast myopic rate shift of right eye;

Countries

China

Contacts

Public ContactBi Hongsheng

Affiliated Eye Hospital of Shandong University of Traditional Chinese Medicine

hongshengbi1@163.com+86 139 5311 3696

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026