NCT07706218

Brief Summary

Refractive error is a common visual disorder encompassing myopia, hyperopia, astigmatism and other subtypes. Refractive error in preschool children refers to refractive abnormalities occurring during the preschool period (0-6 years old). Studies conducted across diverse regions and populations report that the prevalence of refractive error among preschool children ranges approximately from 10% to 30%, with this proportion showing a gradual upward trend in recent years. Existing evidence suggests that preschool refractive status is correlated with multiple ocular and systemic diseases. Furthermore, the preschool years represent a highly sensitive window for children's visual development; uncorrected refractive errors at this stage can disrupt visual maturation and induce permanent visual impairment. Accordingly, identifying the full spectrum of comorbidities associated with preschool refractive error, alongside implementing early diagnosis and intervention, is clinically critical. Nevertheless, substantial challenges persist in the clinical management of preschool refractive errors: the complete comorbidity spectrum remains undefined, its natural history has not been fully elucidated, and high-quality evidence-based guidelines for refractive correction and visual rehabilitation are lacking. Establishing a prospective cohort of preschool children with refractive errors is therefore of great significance for clarifying disease progression and risk factors, generating evidence for standardized refractive interventions and visual rehabilitation protocols, and ultimately preventing visual impairment and improving quality of life in this vulnerable pediatric population. Our research team has previously completed preliminary investigations characterizing myopia in preschoolers. Building on this foundational work, we aim to construct a dedicated cohort of preschool children with refractive errors to delineate the natural history, progression risks and comorbidity profiles of preschool refractive error, and explore effective refractive correction and visual rehabilitation approaches for affected young children.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
28mo left

Started Aug 2026

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 9, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

July 15, 2026

Completed
17 days until next milestone

Study Start

First participant enrolled

August 1, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2028

Last Updated

July 15, 2026

Status Verified

July 1, 2026

Enrollment Period

4 months

First QC Date

July 9, 2026

Last Update Submit

July 9, 2026

Conditions

Keywords

Refractive errorpreschool

Outcome Measures

Primary Outcomes (1)

  • Ocular Biometry Parameters

    A set of objective ocular structural measurements mainly including axial length (AL), alongside corneal curvature, anterior chamber depth, lens thickness and vitreous chamber depth. Axial length, the core indicator in this study, refers to the linear distance from the anterior corneal surface to the retinal pigment epithelium, which is closely associated with the onset and progression of refractive errors in preschool children. All biometric indices will be measured using standardized ophthalmic biometry equipment at each follow-up visit to dynamically observe the developmental rules of ocular dimensions and their correlation with refractive status.

    From date of enrollment until the date of loss to follow-up from any cause, whichever came first, assessed up to 36 months

Secondary Outcomes (5)

  • BCVA

    From date of enrollment until the date of loss to follow-up from any cause, whichever came first, assessed up to 36 months

  • Contrast Sensitivity

    From date of enrollment until the date of loss to follow-up from any cause, whichever came first, assessed up to 36 months

  • SER

    From date of enrollment until the date of loss to follow-up from any cause, whichever came first, assessed up to 36 months

  • WES (Whole Exome Sequencing)

    From date of enrollment until the date of loss to follow-up from any cause, whichever came first, assessed up to 36 months

  • OCT

    From date of enrollment until the date of loss to follow-up from any cause, whichever came first, assessed up to 36 months

Study Arms (1)

Refractive error

Refractive error in preschool children

Eligibility Criteria

Age0 Years - 6 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)
Sampling MethodNon-Probability Sample
Study Population

This study enrolls preschool children aged 0-6 years with refractive errors as the observation group. Eligible subjects meet the following inclusion criteria: refractive error onset during preschool period confirmed by available medical records, spherical power ≤ -0.50 D or ≥ +3.00 D in any meridian, and written informed consent provided by legal guardians. Children who cannot cooperate with ophthalmic examinations and long-term follow-up will be excluded.

You may qualify if:

  • Onset of refractive error occurs during preschool age (0-6 years old) supported by retrievable medical records;
  • Spherical equivalent power ≤ -0.50 D or ≥ +3.00 D in any meridian;
  • Legal guardians agree to participate and sign written informed consent.

You may not qualify if:

  • Children unable to cooperate with examinations and follow-up visits.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Zhongshan Ophthalmic Center Sun Yat-Sen University

Guangdong, Guanzhou, 510060, China

Location

MeSH Terms

Conditions

Refractive Errors

Condition Hierarchy (Ancestors)

Eye Diseases

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
3 Years
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 9, 2026

First Posted

July 15, 2026

Study Start

August 1, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2028

Last Updated

July 15, 2026

Record last verified: 2026-07

Locations