Bifocal Lenses In Nearsighted Kids (BLINK)
Primary Purpose
Refractive Errors
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Biofinity Multifocal D +1.50 add
Biofinity Multifocal D +2.50 add
Biofinity
Sponsored by
About this trial
This is an interventional treatment trial for Refractive Errors focused on measuring pediatrics, refractive error - myopia, contact lenses, intervention
Eligibility Criteria
Inclusion Criteria:
- 7 to 11 years, inclusive, at baseline examination
- -0.75 to -5.00 D, inclusive, spherical component, cycloplegic autorefraction
- ≤1.00 DC, cycloplegic autorefraction
- ≥ 2.00 D difference between the sphere components of the two eyes (anisometropia), cycloplegic autorefraction
- 0.1 logMAR or better best-corrected visual acuity in each eye
- 0.1 logMAR or better visual acuity OU distance and near with a +2.50 D add contact lens
- +2.50 D add lens provides adequate fit with respect to movement and centration
Exclusion Criteria:
- Eye disease or binocular vision problems (e.g., strabismus, amblyopia, oculomotor nerve palsies, corneal disease, etc.)
- Systemic disease that may affect vision, vision development, or contact lens wear (eg, diabetes, Down syndrome, etc.)
- Previous gas permeable, soft bifocal, or orthokeratology contact lens wear or bifocal/PAL spectacle wear (longer than 1 month of wear)
- Previous or current participation in myopia control studies
- Chronic use of medications that may affect immunity, such as oral or ophthalmic corticosteroids for ocular or systemic diseases
- Issues that may interfere with the ability to participate over the next 3 years
Sites / Locations
- Ohio State University College of Optometry
- University of Houston College of Optometry
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Experimental
Experimental
Arm Label
Biofinity
Biofinity Multifocal D +1.50 add
Biofinity Multifocal D +2.50 add
Arm Description
Soft spherical contact lens
The Biofinity Multifocal "D" with a +1.50 add is a soft bifocal contact lens that has a medium reading power
The Biofinity Multifocal "D" with a +2.50 add is a soft bifocal contact lens that has a strong reading power
Outcomes
Primary Outcome Measures
Refractive Error Progression
Refractive error, as measured by cycloplegic autorefraction in both eyes, will be measured yearly to assess the difference in progression between the two soft bifocal treatment lenses (+1.50 D add and +2.50 D add) and the control group (soft spherical contact lenses).
Secondary Outcome Measures
Ocular Shape Change and Eye Growth
The outcome of interest is the change in ocular shape and measured by the change in peripheral refractive error in the right eye. The change in peripheral refractive error will be compared among the two treatment groups and the control group to determine whether peripheral defocus changes the shape of the eye globally (across the whole eye) or locally (specific to the region of the eye affected by the defocus).
Association of Peripheral Defocus to Myopic Progression
Peripheral defocus will be measured in 10 areas (Nasal and temporal zones at 20, 30, and 40 degrees, and superior and inferior zones at 20 and 30 degrees) and analyzed for its relation to myopia progression (as measured by cycloplegic autorefraction in the right eye only).
Axial Length Progression
Axial length progression, as measured by Lenstar in both eyes, will be measured yearly to assess the difference in progression between the two soft bifocal treatment lenses (+1.50 D add and +2.50 D add) and the control group (soft spherical contact lenses).
Full Information
NCT ID
NCT02255474
First Posted
September 23, 2014
Last Updated
February 17, 2021
Sponsor
Ohio State University
Collaborators
University of Houston, National Eye Institute (NEI)
1. Study Identification
Unique Protocol Identification Number
NCT02255474
Brief Title
Bifocal Lenses In Nearsighted Kids
Acronym
BLINK
Official Title
Soft Bifocal Contact Lens Myopia Control
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
September 22, 2014 (Actual)
Primary Completion Date
June 24, 2019 (Actual)
Study Completion Date
June 24, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University
Collaborators
University of Houston, National Eye Institute (NEI)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study will evaluate the use of two different bifocal contact lens add powers to prevent further nearsighted progression in children ages 7 to 11 years old. It is theorized that the profile of the bifocal lenses will decrease the amount of change in nearsightedness that the children experience.
Detailed Description
The primary goal of this project is to determine whether a commercially available soft bifocal contact lens with a distance-center design can slow myopia progression in children. Using soft bifocal contact lenses to manipulate the peripheral optics of the eye is a novel use for a standard contact lens that may keep children from becoming as nearsighted as they would otherwise. Secondary goals are to determine whether the amount of myopic defocus imposed on the peripheral retina by soft bifocal contact lenses is associated in a dose-dependent manner with slowed myopic progression and to determine whether peripheral myopic blur acts to slow eye growth locally or globally. These important pieces of information will enable investigators to learn about the role of peripheral optics for regulating eye growth, which could ultimately lead to optimization of optical signals to slow myopia progression. Ultimately, the information could be used to design optical devices to prevent the onset of myopia in young children.
Slowing myopia progression or eventually preventing myopia onset could potentially affect approximately 60 million children in the United States alone. While the consequences of myopia are rarely sight-threatening, the quality of life for myopic patients is negatively affected and the health care costs to treat myopia are astronomical (approximately $4.6 billion in 1990). The National Eye Institute recognizes the need to "evaluate the efficacy of potential treatments for delaying the onset or for slowing the progression of myopia, such as lenses that alter peripheral defocus."
Using a common treatment of myopia (contact lenses) to potentially slow myopia progression and to learn about optical signals that regulate eye growth is a very novel approach to solving a problem that affects a large proportion of people in the United States.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Refractive Errors
Keywords
pediatrics, refractive error - myopia, contact lenses, intervention
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
294 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Biofinity
Arm Type
Active Comparator
Arm Description
Soft spherical contact lens
Arm Title
Biofinity Multifocal D +1.50 add
Arm Type
Experimental
Arm Description
The Biofinity Multifocal "D" with a +1.50 add is a soft bifocal contact lens that has a medium reading power
Arm Title
Biofinity Multifocal D +2.50 add
Arm Type
Experimental
Arm Description
The Biofinity Multifocal "D" with a +2.50 add is a soft bifocal contact lens that has a strong reading power
Intervention Type
Device
Intervention Name(s)
Biofinity Multifocal D +1.50 add
Intervention Description
This is a monthly disposable contact lens commercially available from CooperVision
Intervention Type
Device
Intervention Name(s)
Biofinity Multifocal D +2.50 add
Intervention Description
This is a monthly disposable contact lens commercially available from CooperVision
Intervention Type
Device
Intervention Name(s)
Biofinity
Intervention Description
This is a monthly disposable spherical contact lens commercially available from CooperVision
Primary Outcome Measure Information:
Title
Refractive Error Progression
Description
Refractive error, as measured by cycloplegic autorefraction in both eyes, will be measured yearly to assess the difference in progression between the two soft bifocal treatment lenses (+1.50 D add and +2.50 D add) and the control group (soft spherical contact lenses).
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Ocular Shape Change and Eye Growth
Description
The outcome of interest is the change in ocular shape and measured by the change in peripheral refractive error in the right eye. The change in peripheral refractive error will be compared among the two treatment groups and the control group to determine whether peripheral defocus changes the shape of the eye globally (across the whole eye) or locally (specific to the region of the eye affected by the defocus).
Time Frame
3 years
Title
Association of Peripheral Defocus to Myopic Progression
Description
Peripheral defocus will be measured in 10 areas (Nasal and temporal zones at 20, 30, and 40 degrees, and superior and inferior zones at 20 and 30 degrees) and analyzed for its relation to myopia progression (as measured by cycloplegic autorefraction in the right eye only).
Time Frame
3 years
Title
Axial Length Progression
Description
Axial length progression, as measured by Lenstar in both eyes, will be measured yearly to assess the difference in progression between the two soft bifocal treatment lenses (+1.50 D add and +2.50 D add) and the control group (soft spherical contact lenses).
Time Frame
3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
11 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
7 to 11 years, inclusive, at baseline examination
-0.75 to -5.00 D, inclusive, spherical component, cycloplegic autorefraction
≤1.00 DC, cycloplegic autorefraction
≥ 2.00 D difference between the sphere components of the two eyes (anisometropia), cycloplegic autorefraction
0.1 logMAR or better best-corrected visual acuity in each eye
0.1 logMAR or better visual acuity OU distance and near with a +2.50 D add contact lens
+2.50 D add lens provides adequate fit with respect to movement and centration
Exclusion Criteria:
Eye disease or binocular vision problems (e.g., strabismus, amblyopia, oculomotor nerve palsies, corneal disease, etc.)
Systemic disease that may affect vision, vision development, or contact lens wear (eg, diabetes, Down syndrome, etc.)
Previous gas permeable, soft bifocal, or orthokeratology contact lens wear or bifocal/PAL spectacle wear (longer than 1 month of wear)
Previous or current participation in myopia control studies
Chronic use of medications that may affect immunity, such as oral or ophthalmic corticosteroids for ocular or systemic diseases
Issues that may interfere with the ability to participate over the next 3 years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey Walline, OD, PhD
Organizational Affiliation
Ohio State University
Official's Role
Study Chair
Facility Information:
Facility Name
Ohio State University College of Optometry
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Facility Name
University of Houston College of Optometry
City
Houston
State/Province
Texas
ZIP/Postal Code
77204
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
35413027
Citation
Gaume Giannoni A, Robich M, Berntsen DA, Jones-Jordan LA, Mutti DO, Myers J, Shaw K, Walker MK, Walline JJ; BLINK Study Group. Ocular and Nonocular Adverse Events during 3 Years of Soft Contact Lens Wear in Children. Optom Vis Sci. 2022 Jun 1;99(6):505-512. doi: 10.1097/OPX.0000000000001902. Epub 2022 Apr 12.
Results Reference
derived
PubMed Identifier
32780139
Citation
Walline JJ, Walker MK, Mutti DO, Jones-Jordan LA, Sinnott LT, Giannoni AG, Bickle KM, Schulle KL, Nixon A, Pierce GE, Berntsen DA; BLINK Study Group. Effect of High Add Power, Medium Add Power, or Single-Vision Contact Lenses on Myopia Progression in Children: The BLINK Randomized Clinical Trial. JAMA. 2020 Aug 11;324(6):571-580. doi: 10.1001/jama.2020.10834.
Results Reference
derived
PubMed Identifier
29561497
Citation
Schulle KL, Berntsen DA, Sinnott LT, Bickle KM, Gostovic AT, Pierce GE, Jones-Jordan LA, Mutti DO, Walline JJ; Bifocal Lenses in Nearsighted Kids (BLINK) Study Group. Visual Acuity and Over-refraction in Myopic Children Fitted with Soft Multifocal Contact Lenses. Optom Vis Sci. 2018 Apr;95(4):292-298. doi: 10.1097/OPX.0000000000001207.
Results Reference
derived
PubMed Identifier
28737608
Citation
Walline JJ, Gaume Giannoni A, Sinnott LT, Chandler MA, Huang J, Mutti DO, Jones-Jordan LA, Berntsen DA; BLINK Study Group. A Randomized Trial of Soft Multifocal Contact Lenses for Myopia Control: Baseline Data and Methods. Optom Vis Sci. 2017 Sep;94(9):856-866. doi: 10.1097/OPX.0000000000001106.
Results Reference
derived
Learn more about this trial
Bifocal Lenses In Nearsighted Kids
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