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Study of Theories About Myopia Progression (STAMP)

Primary Purpose

Myopia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
progressive addition spectacle lens (bifocal)
Single Vision Lenses (SVLs)
Sponsored by
Ohio State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myopia focused on measuring myopia progression, bifocal

Eligibility Criteria

6 Years - 11 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: 6 to 11 years of age Best corrected vision of at least 20/30 in each eye Birth weight > 1250g (The criteria below will be evaluated at a screening visit to find out if the child can participate) Accommodative lag >= 1.30 D (for a 4D stimulus) At least -0.75 D myopia in each meridian measured with cycloplegic autorefraction but not more than -4.50 D in each meridian in each eye Esophoria at near if more than -2.25 D spherical equivalent (high myopia) Astigmatism < 2.00 DC in each eye Anisometropia < 2.00 D Exclusion Criteria: Strabismus (eye turn) History of contact lens wear History of previous bifocal wear Diabetes mellitus

Sites / Locations

  • The Ohio State University College of Optometry

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

PAL

SVL

Arm Description

Progressive Addition Spectacle Lenses (PALs) with a +2.00 D add worn for first year off study. Single Vision Lenses worn for second year of study.

Single Vision Lenses (SVLs) worn both years of the study.

Outcomes

Primary Outcome Measures

Cycloplegic autorefraction

Secondary Outcome Measures

Phoria
Accommodative lag
AC/A ratio
Corneal shape and thickness
Intraocular pressure
Peripheral ocular shape
Central and peripheral aberrations
Crystalline lens thickness and curvature
Anterior chamber depth
Axial length

Full Information

First Posted
June 7, 2006
Last Updated
October 27, 2022
Sponsor
Ohio State University
Collaborators
National Eye Institute (NEI)
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1. Study Identification

Unique Protocol Identification Number
NCT00335049
Brief Title
Study of Theories About Myopia Progression (STAMP)
Official Title
Study of Theories About Myopia Progression (STAMP)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
December 2006 (undefined)
Primary Completion Date
July 2010 (Actual)
Study Completion Date
July 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Ohio State University
Collaborators
National Eye Institute (NEI)

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
At this time, we do not know what causes a child to become more nearsighted (myopic). STAMP will help us better understand nearsightedness in children. Children will be randomly chosen to wear regular glasses (single vision lenses) or no-line bifocal glasses (progressive addition lenses) for the first year of the study. All children will wear regular glasses for the second year of the study. STAMP will compare how the eye changes shape in the two groups to help us understand why children become nearsighted. The two theories of myopia progression that are being evaluated are based on different factors. One theory is based on environmental factors such as extended near work while the other theory is based on genetically coded factors.
Detailed Description
Eligible children will be enrolled, randomized, and followed at six-month intervals for two years with all children wearing single vision lenses for the second year. At each visit, complete measurements of the components of the eye will be made to explain the mechanism responsible for the Progressive Addition Lens (PAL) treatment effect and why it occurs mainly during the first year of bifocal wear (Gwiazda et al. 2003). While hyperopic retinal blur (blur at the back of the eye) due to accommodative lag (poor focusing when doing close work) has been proposed as a possible mechanism driving myopia progression (Gwiazda et al. 1993), others have shown that accommodative lag accompanies rather than precedes the onset of myopia (Mutti et al., 2006). This suggests that accommodative lag is a result of another possible mechanism resulting in myopia progression such as crystalline lens-induced ciliary-choroidal tension (a model in which the lens in the eye is stretched and is not as good at focusing up close) (Mutti et al., 2000). According to this proposed mechanism, high accommodative lag in myopia results from increased crystalline lens tension that is transmitted through the choroid (an outside layer of the eye). This tension results in restricted equatorial (the vertical dimension of the eye) eye growth with no axial (front to back) restriction to eye growth and yields a prolate ocular shape (an eye that is longer than it is wide) in myopes (Mutti et al., 2000). Comparisons: Refractive error (glasses prescription), axial length (length of the eye), peripheral eye shape, accommodation (focusing ability), corneal shape (shape of the front of the eye), anterior chamber depth, crystalline lens thickness and curvatures (shape of the lens in the eye), central and peripheral higher-order aberrations (how well light focuses in the eye), and phoria (eye alignment) will be measured at six-month intervals. The primary study outcome is refractive error measured by cycloplegic autorefraction. Comparison of the biometric data collected both during the first year when the PAL intervention is present and during the second year when the PAL intervention is removed will allow us to differentiate between the two theories under consideration. We will also evaluate whether the modest PAL treatment effect that has been reported during the first year of PAL wear is permanent.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myopia
Keywords
myopia progression, bifocal

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
85 (Actual)

8. Arms, Groups, and Interventions

Arm Title
PAL
Arm Type
Experimental
Arm Description
Progressive Addition Spectacle Lenses (PALs) with a +2.00 D add worn for first year off study. Single Vision Lenses worn for second year of study.
Arm Title
SVL
Arm Type
Active Comparator
Arm Description
Single Vision Lenses (SVLs) worn both years of the study.
Intervention Type
Device
Intervention Name(s)
progressive addition spectacle lens (bifocal)
Other Intervention Name(s)
PAL
Intervention Description
Progressive addition lenses (PAL) with a +2.00 D add.
Intervention Type
Device
Intervention Name(s)
Single Vision Lenses (SVLs)
Other Intervention Name(s)
SVL
Intervention Description
Single vision spectacle lenses.
Primary Outcome Measure Information:
Title
Cycloplegic autorefraction
Time Frame
Baseline, 6, 12, 18, and 24 months
Secondary Outcome Measure Information:
Title
Phoria
Time Frame
Baseline, 6, 12, 18, and 24 months
Title
Accommodative lag
Time Frame
Baseline, 6, 12, 18, and 24 months
Title
AC/A ratio
Time Frame
Baseline, 6, 12, 18, and 24 months
Title
Corneal shape and thickness
Time Frame
Baseline, 6, 12, 18, and 24 months
Title
Intraocular pressure
Time Frame
Baseline, 6, 12, 18, and 24 months
Title
Peripheral ocular shape
Time Frame
Baseline, 6, 12, 18, and 24 months
Title
Central and peripheral aberrations
Time Frame
Baseline, 6, 12, 18, and 24 months
Title
Crystalline lens thickness and curvature
Time Frame
Baseline, 6, 12, 18, and 24 months
Title
Anterior chamber depth
Time Frame
Baseline, 6, 12, 18, and 24 months
Title
Axial length
Time Frame
Baseline, 6, 12, 18, and 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
11 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 6 to 11 years of age Best corrected vision of at least 20/30 in each eye Birth weight > 1250g (The criteria below will be evaluated at a screening visit to find out if the child can participate) Accommodative lag >= 1.30 D (for a 4D stimulus) At least -0.75 D myopia in each meridian measured with cycloplegic autorefraction but not more than -4.50 D in each meridian in each eye Esophoria at near if more than -2.25 D spherical equivalent (high myopia) Astigmatism < 2.00 DC in each eye Anisometropia < 2.00 D Exclusion Criteria: Strabismus (eye turn) History of contact lens wear History of previous bifocal wear Diabetes mellitus
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David A Berntsen, OD, PhD
Organizational Affiliation
University of Houston
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Karla Zadnik, OD, PhD
Organizational Affiliation
Ohio State University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Donald O Mutti, OD, PhD
Organizational Affiliation
Ohio State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Ohio State University College of Optometry
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
8449687
Citation
Gwiazda J, Thorn F, Bauer J, Held R. Myopic children show insufficient accommodative response to blur. Invest Ophthalmol Vis Sci. 1993 Mar;34(3):690-4.
Results Reference
background
PubMed Identifier
12657584
Citation
Gwiazda J, Hyman L, Hussein M, Everett D, Norton TT, Kurtz D, Leske MC, Manny R, Marsh-Tootle W, Scheiman M. A randomized clinical trial of progressive addition lenses versus single vision lenses on the progression of myopia in children. Invest Ophthalmol Vis Sci. 2003 Apr;44(4):1492-500. doi: 10.1167/iovs.02-0816.
Results Reference
background
PubMed Identifier
10752937
Citation
Mutti DO, Sholtz RI, Friedman NE, Zadnik K. Peripheral refraction and ocular shape in children. Invest Ophthalmol Vis Sci. 2000 Apr;41(5):1022-30.
Results Reference
background
PubMed Identifier
16505015
Citation
Mutti DO, Mitchell GL, Hayes JR, Jones LA, Moeschberger ML, Cotter SA, Kleinstein RN, Manny RE, Twelker JD, Zadnik K; CLEERE Study Group. Accommodative lag before and after the onset of myopia. Invest Ophthalmol Vis Sci. 2006 Mar;47(3):837-46. doi: 10.1167/iovs.05-0888.
Results Reference
background
PubMed Identifier
23838771
Citation
Berntsen DA, Barr CD, Mutti DO, Zadnik K. Peripheral defocus and myopia progression in myopic children randomly assigned to wear single vision and progressive addition lenses. Invest Ophthalmol Vis Sci. 2013 Aug 27;54(8):5761-70. doi: 10.1167/iovs.13-11904.
Results Reference
derived
PubMed Identifier
22205604
Citation
Berntsen DA, Sinnott LT, Mutti DO, Zadnik K. A randomized trial using progressive addition lenses to evaluate theories of myopia progression in children with a high lag of accommodation. Invest Ophthalmol Vis Sci. 2012 Feb 13;53(2):640-9. doi: 10.1167/iovs.11-7769. Print 2012 Feb.
Results Reference
derived
PubMed Identifier
20688729
Citation
Berntsen DA, Mutti DO, Zadnik K. The effect of bifocal add on accommodative lag in myopic children with high accommodative lag. Invest Ophthalmol Vis Sci. 2010 Dec;51(12):6104-10. doi: 10.1167/iovs.09-4417. Epub 2010 Aug 4.
Results Reference
derived

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Study of Theories About Myopia Progression (STAMP)

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