- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02458846
Efficacy of Visual Screening in Ontario
March 17, 2020 updated by: Agnes Wong, The Hospital for Sick Children
The Efficacy of a Visual Screening Program to Reduce Later Amblyopia and Untreated Refractive Errors
Amblyopia (lazy eye), is the leading treatable cause of vision loss in childhood.
Uncorrected refractive errors (ie farsightedness) can lead to difficulties in school.
Unfortunately, many children do not receive vision screening until they have already developed irreversible vision problems.
We will conduct a cluster randomized clinical trial in which schools, not individual children, are randomly allocated to receive a kindergarten visual screening program or to receive no intervention by the research team (i.e., "care as usual").
We will compare the prevalence of visual problems (and proportion of children with reading problems) when the children are in Grade 2, after allowing for at least one year of treatment.
Study Overview
Status
Completed
Conditions
Detailed Description
The proposed study is a single-masked cluster randomized clinical trial, with randomization and analyses occurring at the level of "schools" (i.e., we are not randomly assigning individuals to groups).
To assess the efficacy of a visual screening program, we will compare visual outcomes in 25 schools randomly chosen to receive the program and 25 schools allocated to "care as usual" one year after screening.
The screening tools are HOTV crowded acuity, Preschool Randot Stereoacuity Test, and Plusoptix Autorefractor.
The outcome measures will assess later differences between schools receiving the visual screening program and control schools for prevalence of (1) visual and (2) reading problems.
A lower prevalence of either or both problems in schools where the visual screening program was offered would provide evidence for the efficacy of vision screening.
Primary outcome measure is the prevalence of amblyopia, reduced stereo vision, and untreated clinically significant refractive errors in "screened" versus "care as usual" schools.
Secondary outcome measure is the proportion of children performing 1 standard deviation below average on reading scores in "screened" versus "care as usual" schools.
Study Type
Interventional
Enrollment (Actual)
2597
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Ontario
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Toronto, Ontario, Canada, M5G 1X8
- The Hospital for Sick Children
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
3 years to 8 years (CHILD)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Screening: children enrolled in senior kindergarten (age 5-6 years)
- Follow-up: children enrolled in Grade 2 (age 7-8 years)
Exclusion Criteria:
• None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: DIAGNOSTIC
- Allocation: NON_RANDOMIZED
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Screened Schools
25 schools.
Screening involved: crowded HOTV acuity test, Preschool Randot Stereoacuity Test, and Plusoptix autorefractor.
Referral criteria followed AAPOS guidelines for screening for amblyopia and amblyopia risk factors.
Children who fail any one of the three tests (including uncooperative/unable children) will be given a referral letter, which includes an assigned appointment time for a comprehensive eye exam at school with a licensed optometrist.
Any needed glasses will be dispensed at no cost to the parents.
6 months after the eye exam, we will follow up with a phone call to parents to offer any additional support (such as replacing broken/lost glasses)
|
This is one of the most sensitive tests of acuity for vision screening of young children.
The child is asked to recognize a letter (H,O,T,V) that is surrounded by bars to induce the crowding effects typical of amblyopia.
Children were tested monocularly and was required to achieve at least 20/32 in each eye to pass.
Children already wearing glasses were tested with their glasses on.
This is a reliable screening test for stereo depth perception for young children.
Children wear polarized stereoglasses and are asked to identify or match shapes that are "hiding in the snow", which cannot be perceived if the child has abnormal binocular vision.
Children were required to achieve at least 60 arcseconds of disparity to pass.
Children already wearing glasses were tested with their glasses worn under the stereo glasses.
Autorefractors are electronic devices that measure refractive errors by focusing a light onto the child's eyes and recording how their reflections from the retina return to the camera.
The Plusoptix has been shown to have high sensitivity and specificity in previous research.
AAPOS (2013) guidelines were used to determine the referral criteria.
Children who did not pass all three screening tests were referred for full cycloplegic optometry exams, with a parent/guardian present.
Optometrists assessed visual history, monocular visual acuity (near & far), strabismus, binocular function, abnormalities of the anterior segment, and cycloplegic refraction.
If the optometrist prescribed glasses, frames were chosen at the time of the exam and the glasses were dispensed either at school (with an optician) or at the optometrist's office.
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No Intervention: Care As Usual Schools
25 schools were randomly allocated to the "care as usual" schools.
No intervention was provided by the research team, however, children may have received optometry/ophthalmology care via regular referral channels (e.g., family physicians, teachers)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevalence of amblyopia
Time Frame: 16 months
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Prevalence of suspected amblyopia, defined as 2-or-greater line difference in acuity between eyes
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16 months
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Prevalence of refractive errors
Time Frame: 16 months
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Untreated clinically significant refractive errors defined by AAPOS (2013) guidelines
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16 months
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Prevalence of reduced stereo vision
Time Frame: 16 months
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Stereoacuity is often reduced in patients with some types of amblyopia, and will defined as worse than 30 arcsec
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16 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Proportion of below-average readers Year 1
Time Frame: 10 months
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Proportion of Grade 1 children reading 1 SD below average
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10 months
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Proportion of below-average readers Year 2
Time Frame: 22 months
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Proportion of Grade 2 children reading 1 SD below average
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22 months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Agnes Wong, The Hospital for Sick Children
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2014
Primary Completion (Actual)
December 15, 2019
Study Completion (Actual)
December 15, 2019
Study Registration Dates
First Submitted
January 8, 2015
First Submitted That Met QC Criteria
May 27, 2015
First Posted (Estimate)
June 1, 2015
Study Record Updates
Last Update Posted (Actual)
March 19, 2020
Last Update Submitted That Met QC Criteria
March 17, 2020
Last Verified
March 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1000045972
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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