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Cohort Study on Co-Prevention of Multiple Morbidities in School-Age Children by “Sunlight Eye Care”

Cohort Study on Co-Prevention of Multiple Morbidities in School-Age Children by “Sunlight Eye Care”

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122357
Enrollment
Unknown
Registered
2026-04-13
Start date
2024-12-14
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Myopiasystemic diseasepyscology

Interventions

Control group:none
Intervention group:Group behavior intervention

Sponsors

Shenzhen Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 11 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion Criteria for Study Population: (1) Primary schools in various districts of Shenzhen listed on the roster, randomly selected based on regional distribution; (2) School leadership voluntarily participates in this study and is able to cooperate with the implementation of the research. 2. Inclusion Criteria for Participants: (1) School-age children enrolled in grades one to two of the selected primary schools; (2) Both genders, aged 6 to 11 years; (3) Voluntary participation in this study, with informed consent signed by the participant's legal guardian.

Exclusion criteria

Exclusion criteria: 1. Exclusion Criteria for Study Population: (1) Schools in Shenzhen that are not primary schools; (2) Already participating in other eye disease-related clinical research projects that conflict with this study; (3) Those who refuse to participate in this study; (4) Those deemed unsuitable by the researchers. 2. Exclusion Criteria for Participants: (1) Subjects with eye diseases (excluding refractive errors and allergic conjunctivitis), such as hereditary eye diseases, congenital cataracts, glaucoma, keratopathy, etc.; (2) Those with a recent history of ocular surgery; (3) Those with a recent history of ocular trauma; (4) Those with severe systemic diseases, such as nephropathy, leukemia, etc.; (5) Those unable to cooperate due to psychiatric factors, etc.; (6) Those whose legal guardians refuse to participate in this study; (7) Those deemed unsuitable by the researchers.

Design outcomes

Primary

MeasureTime frame
SE;Annual Change in Refraction (Spherical Equivalent);Changes in Ocular Structural Biometric Parameters (Axial Length, Corneal Curvature, Corneal Thickness, Anterior Chamber Depth, Lens Thickness, Lens Curvature);

Secondary

MeasureTime frame
Annual Change in Refraction (Spherical Equivalent);Scores;Mental health;Biometric outcomes;Whole-body health;

Countries

China

Contacts

Public ContactGuoming Zhang

Shenzhen Eye Hospital

zhang-guoming@163.com+86 138 2350 9060

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026