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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05691296
Other study ID # Tianjin myopia Intervention
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 1, 2020
Est. completion date December 31, 2024

Study information

Verified date May 2024
Source Tianjin Eye Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aimed to collect multi-factor information on school-age children with pre-clinical myopia, and to identify the initial factors and warning signs of myopia.


Description:

The incidence of myopia is high in China. At present, the mechanism of myopia is unclear, and the main theories are genetic and environmental aspects. Many factors may affect the occurrence and development of myopia in students, such as ocular biological parameters, peripheral refractive state, differences in binocular vision function, eye habits, and outdoor time. In this study, the multi-factor information on pre-clinical myopia in school-age children was collected to find out the initial factors and warning signals of myopia.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 4000
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 5 Years to 12 Years
Eligibility Inclusion Criteria: - All students in grades 1 to 4 - Can cooperate with the examination of students Exclusion Criteria: - Obvious strabismus and amblyopia - Eye diseases that affect vision, such as congenital cataracts, glaucoma, and retinal diseases - History of ocular surgery

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Home training
Letter Chart Accomodative Rock Training for 2 minutes each time
School training
Letter Chart Accomodative Rock Training for 2 minutes each time

Locations

Country Name City State
China Tiajin Eye Hospital Tianjin Tianjin

Sponsors (1)

Lead Sponsor Collaborator
Tianjin Eye Hospital

Country where clinical trial is conducted

China, 

References & Publications (1)

Jonas JB, Ang M, Cho P, Guggenheim JA, He MG, Jong M, Logan NS, Liu M, Morgan I, Ohno-Matsui K, Parssinen O, Resnikoff S, Sankaridurg P, Saw SM, Smith EL 3rd, Tan DTH, Walline JJ, Wildsoet CF, Wu PC, Zhu X, Wolffsohn JS. IMI Prevention of Myopia and Its Progression. Invest Ophthalmol Vis Sci. 2021 Apr 28;62(5):6. doi: 10.1167/iovs.62.5.6. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary The rate of new-onset myopia The number of new children with myopia was counted Through study completion, an average of 1 year
Primary The changes of refractive error The changes of refractive error between visit time and baseline which was obtained with a computer refractometer. Every 6 months, up to 3 years
Primary The changes of axial length The axial length was measured by a biological measuring instrument. Every 6 months, up to 3 years
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