Myopia Prevalence in Canadian School Children - a Pilot Study

NCT ID: NCT01942057

Last Updated: 2015-07-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

173 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-12-31

Study Completion Date

2015-04-30

Brief Summary

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The goal of this study is to determine the prevalence of nearsightedness in Canadian school children living in the Waterloo Region.

Detailed Description

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Conditions

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Myopia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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School Grades 1+2

Children currently enrolled in grades 1 and 2

No interventions assigned to this group

School Grades 6+7

Children currently enrolled in grades 6 and 7

No interventions assigned to this group

School Grades 11+12

Children currently enrolled in grades 11 and 12

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Has had a parent/legal guardian read the study consent form and who agrees to allow them to participate in the study by signing the consent form
* Has had the "letter of assent for children" explained to them, the child has agreed to participate and the letter has been signed by the study investigator and the child
* Has provided the completed Questionnaire (Appendix 4A for parents to complete on behalf of their children in school grades 1 and 2, 6 and 7; Appendix 4B for children to complete that are in school grades 11 and 12)
* Is currently in school grades 1 and 2, 6 and 7 or 11 and 12
* Is willing and able to follow instructions and maintain the appointment schedule

Exclusion Criteria

* Has not given verbal assent to participate
* Has known sensitivity to the diagnostic pharmaceuticals to be used in the study
* Has undergone refractive error surgery or orthokeratology
* Has serious medical disorders or eye diseases/abnormalities such as amblyopia and cataract or a cognitive inability to conduct the tests
Minimum Eligible Age

6 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Waterloo

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Lyndon Jones, PhD

Role: PRINCIPAL_INVESTIGATOR

Center for Contact Lens Research

Locations

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Centre for Contact Lens Research

Waterloo, Ontario, Canada

Site Status

Countries

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Canada

Related Links

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http://cclr.uwaterloo.ca/

Centre for Contact Lens Research Website

Other Identifiers

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19043

Identifier Type: -

Identifier Source: org_study_id

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