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Clinical Trials/NCT02903628
NCT02903628CompletedNot Applicable

Vice-president, Nurse, Principal Investigator

Wenzhou Medical University0 sites1,517 target enrollmentStarted: June 2012Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
1,517
Primary Endpoint
Prevalence of Myopia

Study Overview

Brief Summary

The purpose of this study is to determine whether Eye Health Intervention can obviously reduce and delay myopia onset and development and improved the awareness rate of knowledge apparently .

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
6 Years to 14 Years (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • primary 1-3 grade students

Exclusion Criteria

  • ocular inflammation
  • eye injury
  • dysgnosia

Outcomes

Primary Outcomes

Prevalence of Myopia

Time Frame: every 6 months, total 3 years

Secondary Outcomes

  • health of eyes behavior(every 6 months, total 3 years, questionnaire)
  • health of eyes knowledge(every 6 months, total 3 years, questionnair)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Chen yanyan

Vice-president, Nurse, Principal Investigator

Wenzhou Medical University

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