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Effect of MyopiaEd Messaging on Improving Eye-use Behavior and Myopia Control Among Primary School Students in China

Effect of MyopiaEd Messaging on Improving Eye-use Behavior and Myopia Control Among Primary School Students in China: A Randomized Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07211893
Enrollment
1330
Registered
2025-10-08
Start date
2025-12-05
Completion date
2026-12-31
Last updated
2025-12-10

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

Conditions

Myopia

Brief summary

Myopia represents a significant global public health challenge, with China experiencing particularly high myopia prevalence among children and adolescents. The World Health Organization (WHO) acknowledges the critical role of health education in eye care and has collaborated with the International Telecommunication Union (ITU) to launch the Be He@lthy, Be Mobile (BHBM) initiative, which includes MyopiaEd-a mobile health project specifically designed to address myopia. Developed in partnership with international experts and informed by evidence-based guidelines, MyopiaEd provides standardized, scientifically validated content for effective myopia control. The MyopiaEd library has been translated and adapted by the Zhongshan Ophthalmic Center for use in China. Therefore, we aim to investigate whether the Chinese version of MyopiaEd can improve eye care behaviors among primary school students and enhance parental knowledge regarding myopia prevention and control in China.

Interventions

OTHERSend myopia-related health education message

Guardians of students in the intervention group will receive regular myopia-related health education messages, comprising text and images, from the MyopiaEd information repository via class-based WeChat groups. The intervention will last for 12 months.

Sponsors

National Health Commission of the People's Republic of China
CollaboratorUNKNOWN
Zhongshan Ophthalmic Center, Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
8 Years to 12 Years
Healthy volunteers
Yes

Inclusion criteria

* primary school students in the third grade; * the guardians of students can receive, read, and understand multimedia (image-text) messages via WeChat on their mobile phones; * voluntary participation in this study, with guardians' consent and a signed informed consent form.

Exclusion criteria

* with other ocular diseases that severely affect vision * with systematic diseases or mental disorders, inability to understand or cooperate with the study

Design outcomes

Primary

MeasureTime frameDescription
The proportion of children having improved eye-use behaviors after 1 year.12 monthsChildren are considered to have improved behaviors if they meet three or more of the following criteria after 12 months: Outdoor Time: Increase of ≥ 30 minutes for those initially \< 2 hours; maintain ≥ 2 hours for those initially ≥ 2 hours. Near Work Time: Reduce ≥ 30 minutes for those initially ≥ 1 hour; maintain \< 1 hour for those initially \< 1 hour. Screen Time: Reduce ≥ 30 minutes for those initially ≥ 1 hour; maintain \< 1 hour for those initially \< 1 hour. Eye Exam Frequency: Increase of ≥ 1 exam for those with \< 2 exams initially; maintain ≥ 2 for those with ≥ 2 exams. Sitting Posture: Increase of ≥ 1 point for those with ≤ 3; maintain ≥ 4 for those with ≥ 4. Resting Behavior During Near Work: Increase of ≥ 1 point for those with ≤ 3; maintain ≥ 4 for those with ≥ 4. Spectacle-Wearing: Children not wearing glasses begin after 12 months. Daily Spectacle Wear for Myopic Children: Increase of ≥ 1 hour for those wearing ≤ 8 hours; maintain \> 8 hours for those wearing \> 8 hour.

Secondary

MeasureTime frameDescription
Change in myopia-related knowledge score of students' guardians between baseline and 12 months12 monthsChange in myopia-related knowledge score of students' guardians between baseline and 12 months, assessed via questionnaire. The score ranged from 1 to 20, with higher scores indicating better knowledge.
Difference in incidence of myopia between the two groups after 12 months12 monthsDifference in incidence of myopia between the two groups after 12 months
Difference in the change of spherical equivalence between baseline and 12 months in the two groups12 monthsDifference in the change of spherical equivalence between baseline and 12 months in the two groups. Spherical equivalence is calculated as sphere plus half of cylindrical power, as assessed by auto-refraction.
The satisfaction of the MyopiaEd information by the guardians12 monthsThe satisfaction of the MyopiaEd information by the guardians, assessed by a study questionnaire. Satisfaction score ranges from 1 to 5, with higher scores indicating better satisfaction.

Contacts

Primary ContactLingyi Liang
lianglingyi@gzzoc.com+8602087330487

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026