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Effect of Using Myopia Prediction Algorithm on Myopia School-aged Children

Primary Purpose

Myopia

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Myopia prediction algorithm
Sponsored by
Sun Yat-sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Myopia focused on measuring Vision Disorders, Artificial intelligence, Myopia prediction

Eligibility Criteria

8 Years - 10 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Children aged 8-10
  • Has the record of eye refraction examined in the past year, SER<-0.5D
  • Current BCVA≥0.8, SER<-0.5D, Astigmatism less than 1.50 D, anisometropia less than 1.50 D
  • Written informed consents provided

Exclusion Criteria:

  • Definitive diagnosis of other diseases except for refractive error
  • Previous eye surgery
  • Previous usage of orthokeratology lenses and atropine
  • Unwilling to participate in this trial

Sites / Locations

  • Zhongshan Ophthalmic CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Using myopia prediction algorithm

Not using myopia prediction algorithm

Arm Description

After examination of visual acuity, eye refraction and biometrics, the examination results are shown to the children. Meanwhile, myopia prediction algorithm will be used to predict SER at 3 years.

After examination of visual acuity, eye refraction and biometrics, the examination results are shown to the children.

Outcomes

Primary Outcome Measures

Incidence of SER development of at least -1.0 dioptres (D)
SER: spherical equivalent refraction, sphere + ½ 360 cylinder; SER development of at least -1.0 dioptres: SER2 - SER1≤-0.5D; SER1: SER at baseline; SER2: SER up to 2 year
Incidence of SER development of at least -0.5 dioptres (D)
SER: spherical equivalent refraction, sphere + ½ 360 cylinder; SER development of at least -0.5 dioptres: SER2 - SER1≤-0.5D; SER1: SER at baseline; SER2: SER up to 1 year

Secondary Outcome Measures

Changes in SER \ and AL
Changes in SER \ and AL will be calculated; AL: axial length
Changes in SER \ and AL
Changes in SER \ and AL will be calculated; AL: axial length
Changes in proportion of children using atropine
Changes in proportion of children using atropine will be calculated
Changes in proportion of children using atropine
Changes in proportion of children using atropine will be calculated
Changes in proportion of children using orthokeratology lenses
Changes in proportion of children using orthokeratology lenses will be calculated
Changes in proportion of children using orthokeratology lenses
Changes in proportion of children using orthokeratology lenses will be calculated
Changes in proportion of children using spectacles
Changes in proportion of children using spectacles will be calculated
Changes in proportion of children using spectacles
Changes in proportion of children using spectacles will be calculated
Changes in child's average outdoor activity time per day
Changes in child's average outdoor activity time per day will be calculated
Changes in child's average outdoor activity time per day
Changes in child's average outdoor activity time per day will be calculated
Changes in child's average screen time per day
Changes in child's average screen time per day will be calculated
Changes in child's average screen time per day
Changes in child's average screen time per day will be calculated

Full Information

First Posted
August 2, 2019
Last Updated
August 6, 2019
Sponsor
Sun Yat-sen University
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1. Study Identification

Unique Protocol Identification Number
NCT04045951
Brief Title
Effect of Using Myopia Prediction Algorithm on Myopia School-aged Children
Official Title
Effect of Using Myopia Prediction Algorithm on Myopia School-aged Children's Eye Refraction in China: a Multi-center Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Unknown status
Study Start Date
August 3, 2019 (Actual)
Primary Completion Date
November 30, 2021 (Anticipated)
Study Completion Date
November 30, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sun Yat-sen University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In this study, the investigators aim to perform a prospective, randomized controlled study to compare the myopia development between myopia children using myopia prediction algorithm and myopia children without using myopia prediction algorithm
Detailed Description
The investigators propose to enroll myopia children aged 8-10 in China. Children will be given examinations of visual acuity, eye refraction and biometrics, and be assigned to two groups: participants in group A use myopia prediction algorithm to predict myopia development, while in Group B, the participants do not use myopia prediction algorithm to predict myopia development. The visual acuity, eye refraction and biometrics will be investigated over the one-year follow-up period, aiming at comparison of actual myopia development between the two groups

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myopia
Keywords
Vision Disorders, Artificial intelligence, Myopia prediction

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
The outcomes assessors involved in data management and analysis will be blinded to the group assignment. The study participants, the investigators responsible for randomization will not be masked.
Allocation
Randomized
Enrollment
2138 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Using myopia prediction algorithm
Arm Type
Experimental
Arm Description
After examination of visual acuity, eye refraction and biometrics, the examination results are shown to the children. Meanwhile, myopia prediction algorithm will be used to predict SER at 3 years.
Arm Title
Not using myopia prediction algorithm
Arm Type
No Intervention
Arm Description
After examination of visual acuity, eye refraction and biometrics, the examination results are shown to the children.
Intervention Type
Other
Intervention Name(s)
Myopia prediction algorithm
Intervention Description
Candidate predictors included age at examination, SER, and annual progression rate. Using these predictors, the algorithm will be used to predict SER at 3 years.
Primary Outcome Measure Information:
Title
Incidence of SER development of at least -1.0 dioptres (D)
Description
SER: spherical equivalent refraction, sphere + ½ 360 cylinder; SER development of at least -1.0 dioptres: SER2 - SER1≤-0.5D; SER1: SER at baseline; SER2: SER up to 2 year
Time Frame
up to 2 year
Title
Incidence of SER development of at least -0.5 dioptres (D)
Description
SER: spherical equivalent refraction, sphere + ½ 360 cylinder; SER development of at least -0.5 dioptres: SER2 - SER1≤-0.5D; SER1: SER at baseline; SER2: SER up to 1 year
Time Frame
up to 1 year
Secondary Outcome Measure Information:
Title
Changes in SER \ and AL
Description
Changes in SER \ and AL will be calculated; AL: axial length
Time Frame
Up to 1 year
Title
Changes in SER \ and AL
Description
Changes in SER \ and AL will be calculated; AL: axial length
Time Frame
Up to 2 year
Title
Changes in proportion of children using atropine
Description
Changes in proportion of children using atropine will be calculated
Time Frame
Up to 1 year
Title
Changes in proportion of children using atropine
Description
Changes in proportion of children using atropine will be calculated
Time Frame
Up to 2 year
Title
Changes in proportion of children using orthokeratology lenses
Description
Changes in proportion of children using orthokeratology lenses will be calculated
Time Frame
Up to 1 year
Title
Changes in proportion of children using orthokeratology lenses
Description
Changes in proportion of children using orthokeratology lenses will be calculated
Time Frame
Up to 2 year
Title
Changes in proportion of children using spectacles
Description
Changes in proportion of children using spectacles will be calculated
Time Frame
Up to 1 year
Title
Changes in proportion of children using spectacles
Description
Changes in proportion of children using spectacles will be calculated
Time Frame
Up to 2 year
Title
Changes in child's average outdoor activity time per day
Description
Changes in child's average outdoor activity time per day will be calculated
Time Frame
Up to 1 year
Title
Changes in child's average outdoor activity time per day
Description
Changes in child's average outdoor activity time per day will be calculated
Time Frame
Up to 2 year
Title
Changes in child's average screen time per day
Description
Changes in child's average screen time per day will be calculated
Time Frame
Up to 1 year
Title
Changes in child's average screen time per day
Description
Changes in child's average screen time per day will be calculated
Time Frame
Up to 2 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Children aged 8-10 Has the record of eye refraction examined in the past year, SER<-0.5D Current BCVA≥0.8, SER<-0.5D, Astigmatism less than 1.50 D, anisometropia less than 1.50 D Written informed consents provided Exclusion Criteria: Definitive diagnosis of other diseases except for refractive error Previous eye surgery Previous usage of orthokeratology lenses and atropine Unwilling to participate in this trial
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yahan Yang
Phone
+8615521013933
Email
yah.yang39@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Haotian Lin
Phone
+8613802793086
Email
haot.lin@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Haotian Lin
Organizational Affiliation
Zhongshan Ophthalmic Center, Sun Yat-sen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Zhongshan Ophthalmic Centre
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510623
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yahan Yang
Phone
+86-15521013933

12. IPD Sharing Statement

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Effect of Using Myopia Prediction Algorithm on Myopia School-aged Children

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