Ignite Creation Date:
2025-12-25 @ 1:17 AM
Ignite Modification Date:
2025-12-25 @ 11:26 PM
Study NCT ID:
NCT04740593
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2025-08-11
First Post:
2021-01-14
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
The Effect of Early Glasses on the Development of Amblyopia
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D000550', 'term': 'Amblyopia'}, {'id': 'D012030', 'term': 'Refractive Errors'}], 'ancestors': [{'id': 'D001927', 'term': 'Brain Diseases'}, {'id': 'D002493', 'term': 'Central Nervous System Diseases'}, {'id': 'D009422', 'term': 'Nervous System Diseases'}, {'id': 'D014786', 'term': 'Vision Disorders'}, {'id': 'D012678', 'term': 'Sensation Disorders'}, {'id': 'D009461', 'term': 'Neurologic Manifestations'}, {'id': 'D005128', 'term': 'Eye Diseases'}, {'id': 'D012816', 'term': 'Signs and Symptoms'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D005139', 'term': 'Eyeglasses'}], 'ancestors': [{'id': 'D007909', 'term': 'Lenses'}, {'id': 'D055096', 'term': 'Optical Devices'}, {'id': 'D004864', 'term': 'Equipment and Supplies'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['OUTCOMES_ASSESSOR'], 'maskingDescription': 'The outcome assessor will only have access to coded data, which cannot be traced back to the individual participants, from the electronic Case Report Forms in Castor, a cloud-based clinical data management platform.'}, 'primaryPurpose': 'PREVENTION', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 601}}, 'statusModule': {'overallStatus': 'ACTIVE_NOT_RECRUITING', 'startDateStruct': {'date': '2021-05-10', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-08', 'completionDateStruct': {'date': '2026-03-31', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-08-05', 'studyFirstSubmitDate': '2021-01-14', 'studyFirstSubmitQcDate': '2021-02-04', 'lastUpdatePostDateStruct': {'date': '2025-08-11', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2021-02-05', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2026-03-31', 'type': 'ESTIMATED'}}, 'outcomesModule': {'otherOutcomes': [{'measure': 'Electronically measured compliance with spectacles wearing', 'timeFrame': 'Yet to be defined, probably time = 12-24 months', 'description': 'During home visits an Occlusion Dose Monitor (ODM) will be fixed firmly to the spectacles next to the temple by imbedding the ODM in an occlusion eye patch for one week. After one week it will be removed during a subsequent home visit and the recording will be downloaded.'}, {'measure': 'The evolution of hyperopia, anisometropia and astigmatism, all three based on the means of these three types of discrete variables, measured repeatedly between age 1 and 4 by retinoscopy in cycloplegia in all children with high refractive error at age 1.', 'timeFrame': 'First to final examination, time = 0 to 30-36 months', 'description': 'It involves three longitudinal outcome measures, based on the repeated measurement of the three types of refractive errors that are of interest for this study from age 1 to 4 (each potentially stratified for severity of refractive error at age 1). A Mixed Model linear regression model will be use to correct for inner participant data clustering.'}, {'measure': 'Family history for ocular disease', 'timeFrame': 'First examination, time = 0', 'description': 'Anamnesis'}, {'measure': 'Ethnicity', 'timeFrame': 'First examination, time = 0', 'description': 'Anamnesis'}, {'measure': 'Parental level of education, social economic status and language skill', 'timeFrame': 'First examination, time = 0', 'description': 'Anamnesis'}, {'measure': 'Gender', 'timeFrame': 'First examination, time = 0', 'description': 'Anamnesis'}], 'primaryOutcomes': [{'measure': 'The occurrence of amblyopia at the final examination, stratified according to visual acuity of the amblyopic eye in the intervention group (group 1) and in the control group (group 2)', 'timeFrame': 'Final examination, time = 30-36 months', 'description': "The prevalence of amblyopia at age 4 stratified according to visual acuity of the amblyopic eye in the intervention group (group 1) and the control group (group 2) at the final examination. When a child is diagnosed with amblyopia during the course of the study, the child's visual acuity at the moment of referral will be used as primary outcome, after correcting for age."}], 'secondaryOutcomes': [{'measure': 'Prevalence of amblyopia at age 1', 'timeFrame': 'First examination, time = 0', 'description': 'Defined/noted by study orthoptist'}, {'measure': 'Type and magnitude of refractive error at age 1', 'timeFrame': 'First examination, time = 0', 'description': 'Measured by retinoscopy in cyloplegia'}, {'measure': 'Occurrence of amblyopia at age 4 stratified according to visual acuity of the amblyopic eye at the final examination in the children without refractive error at age 1 (group 2 and 3).', 'timeFrame': 'Final examination, time = 30-36 months', 'description': 'Defined/noted by study orthoptist'}, {'measure': 'Pre-literacy skills in the intervention and control group at age 4', 'timeFrame': 'Final examination, time = 30-36 months', 'description': 'Measured with the Test of Preschool Early Literacy (TOPEL)'}, {'measure': 'In all groups, occurrence of strabismus at the final examination', 'timeFrame': 'Final examination, time = 30-36 months', 'description': 'Defined/noted by study orthoptist'}]}, 'oversightModule': {'isUsExport': False, 'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['Glasses', 'Vision screening'], 'conditions': ['Amblyopia', 'Refractive Errors']}, 'referencesModule': {'references': [{'pmid': '14566312', 'type': 'BACKGROUND', 'citation': 'Donahue SP, Arnold RW, Ruben JB; AAPOS Vision Screening Committee. Preschool vision screening: what should we be detecting and how should we report it? Uniform guidelines for reporting results of preschool vision screening studies. J AAPOS. 2003 Oct;7(5):314-6. doi: 10.1016/s1091-8531(03)00182-4. No abstract available.'}]}, 'descriptionModule': {'briefSummary': 'In a randomized controlled trial, we will establish whether early glasses for high refractive error at age one reduce the development of amblyopia between age one and four. As a secondary outcome early literacy will be compared in groups with and without glasses.', 'detailedDescription': "Background of the study:\n\nAmblyopia (prevalence approx. 3.4%) develops in early childhood when the child's eyes have severe refractive error, when they squint, or both. It can effectively be treated with glasses and patching the better eye, but treatment should start before age 6 to be effective. Therefore, visual acuity should be measured in all children aged 4-5 to detect amblyopia early enough. In an effort to prevent the development of amblyopia all together, in some countries devices are being used to measure refractive error in toddlers and, when refractive error is severe, fit them glasses before amblyopia develops. In Flanders, the measurement of refractive error in 1- and 2.5-year-olds began in 2012, in addition to regular vision screening with measurement of the visual acuity at the age of 3, 4 and 5. Between 2012 and 2017 the percentage of 4-year-old glasses wearing children had risen from 4.7% to 6.4%, but it was unknown how many cases of amblyopia had been prevented from developing. A prospective comparison seems warranted between this new method and the current national vision screening program in the Netherlands.\n\nObjective of the study:\n\nTo investigate whether treating children with high refractive errors at age one with glasses prevents the development of amblyopia.\n\nStudy design:\n\nWe will perform an interventional prevention study comparing the effect of prescribing glasses to children with high refractive error at age 1 (intervention) versus no prescription of glasses (control) on the prevalence of amblyopia at age 4. 12-18-months-old children will be recruited by the study physician after visiting the children's healthcare centers (CHCs) at 11 or 14 months. Refractive error will be determined by retinoscopy in cycloplegia in all children. Children with refractive error exceeding the AAPOS 2003 criteria (Donahue et al. 2003) are considered to have high refractive error in this study. We anticipate that 8% of all children will have high refractive error according to these criteria. These children will be randomized to the intervention group or the control group, and will be followed up until final examination at age 4 with visual acuity serving as primary outcome. In case amblyopia or strabismus develops during the course of the study, children will be referred for immediate treatment, and visual acuity at the moment of referral will be used as primary outcome. In all children in the intervention group compliance with wearing spectacles will be measured electronically. At age 4 pre-literacy skills will be measured in the intervention group and the control group.\n\nThe majority of children, approximately 92%, will have mild or no refractive error at age one. After the first examination, these children will continue regular vision screening at the CHCs. They will have their visual acuity measured at the age of 4 as part of standard vision screening in the Netherlands at the CHCs, which will serve as secondary outcome. If there is uncertainty about the visual outcome at the CHC, the child will receive a supplementary examination. Children with amblyopia or strabismus at the age of one will be excluded from this study and referred for immediate treatment. Due to ethical considerations, children with severe refractive error at the age of one, i.e. exceeding the AAPOS 2003 criteria twofold, will also be excluded from this study and referred for immediate treatment with glasses. Due the nature and design of the study, blinding of the researchers on site and of participants will not be possible.\n\nStudy population:\n\nFor this study we will recruit an estimated 2000-4000 healthy children aged 12-18 months after visiting one of the participating CHCs, located in different regions of the Netherlands: Utrecht, Harderwijk/Ermelo/Putten, Tiel/Geldermalsen/Culemborg,Roermond/Venlo and Eindhoven. It is estimated that approximately 8% of all included children will have high refractive error.\n\nIntervention (if applicable):\n\nChildren assigned to the intervention group will be examined by the study orthoptist one to three times yearly until final examination, and will be fitted with glasses, based on accurate determinations of refractive error by retinoscopy in cycloplegia. Children with high refractive error assigned to the control group will be examined by the study orthoptist one to three times yearly until final examination, but will not be fitted with glasses.\n\nPrimary study parameters/outcome of the study:\n\nThe occurrence of amblyopia at the final examination, stratified according to visual acuity of the amblyopic eye in the intervention group and in the control group. The final examination will take place at the age of 4, unless children have been referred to an orthoptist and/or ophthalmologist before, for example when amblyopia or strabismus are suspected before the age of 4.\n\nSecondary study parameters/outcome of the study:\n\n* Prevalence of amblyopia at age 1;\n* Type and severity of refractive error at age 1;\n* Occurrence of amblyopia at the final examination, stratified according to visual acuity of the amblyopic eye in the children without high refractive error at age 1;\n* Pre-literacy skills in the intervention and control group at age 4;\n* Occurrence of strabismus, determined at the final examination in all groups.\n\nOther outcome measures:\n\n* Electronically measured compliance with spectacles wearing;\n* The evolution of refractive error between age 1 and 4;\n* Gender;\n* Family history for ocular disease;\n* Ethnicity;\n* Parental level of education, social economic status and language skill.\n\nNature and extent of the burden and risks associated with participation, benefit and group relatedness:\n\nThe expected burden and risks associated with participation can be considered minimal. In order to measure refractive error accurately, retinoscopy will be done by study orthoptists after the instillation of cycloplegic eye drops, as happens daily in clinical practice of orthoptists and pediatric ophthalmologists. We will install 1 eyedrop of cyclopentolate 1% in each eye, which we will repeat after 10 minutes. Cyclopentolate can cause sleepiness in rare cases: children are difficult to awaken for several minutes, but can be awoken thereafter, which is without sequelae without exception."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD'], 'maximumAge': '18 Months', 'minimumAge': '12 Months', 'healthyVolunteers': True, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Registered at one of the participating CHCs;\n* 12-18 months of age;\n* Voluntary approval for participation by the parents or legal representative/guardian with provided written informed consent;\n* Willingness of the parents/guardian(s) to comply with the study procedures\n\nExclusion Criteria:\n\n* Congenital syndromes;\n* Psychomotor retardation;\n* Known hereditary defects;\n* Known cardiac disease;\n* Severe comorbidity;\n* Children's whose parents do not agree to cyclopegia with the use of cyclopentolate 1% eye drops for orthoptic examination (retinacopy) by the study orthoptist;\n* Refractive error higher than the AAPOS criteria twofold (i.e. hyperopia \\>7 dioptres, anisometropia \\>3 dioptres and astigmatism of \\>3 dioptres at 90º or 180º and \\>2 dioptres in oblique axis (\\>10º eccentric to 90º or 180º);\n* Strabismus;\n* Amblyopia;\n* Ptosis;\n* Cataract or other media opacity;\n* Other ophthalmic disease requiring immediate referral;"}, 'identificationModule': {'nctId': 'NCT04740593', 'acronym': 'EGS', 'briefTitle': 'The Effect of Early Glasses on the Development of Amblyopia', 'organization': {'class': 'OTHER', 'fullName': 'Erasmus Medical Center'}, 'officialTitle': 'The Early Glasses Study: Can Early Glasses Prevent the Development of Amblyopia in Children With High Refractive Errors at Age One', 'orgStudyIdInfo': {'id': 'ABR number: 76412'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Group 1 - High refractive error: Intervention', 'description': 'Children with high refractive error (i.e. exceeding the AAPOS 2003 criteria) at age one, who are randomly assigned to the intervention group', 'interventionNames': ['Other: Orthoptic care with the prescription of glasses from age 12-18 months onwards']}, {'type': 'OTHER', 'label': 'Group 2 - High refractive error: Control', 'description': 'Children with high refractive error (i.e. exceeding the AAPOS 2003 criteria) at age one, who are randomly assigned to the control group', 'interventionNames': ['Other: Orthoptic care without the prescription of glasses from age 12-18 months onwards']}, {'type': 'OTHER', 'label': 'Group 3 - Mild or no refractive error', 'description': 'Children with mild or no refractive error (i.e. not exceeding the AAPOS 2003 criteria) at age one', 'interventionNames': ['Other: First measurement only']}], 'interventions': [{'name': 'Orthoptic care with the prescription of glasses from age 12-18 months onwards', 'type': 'OTHER', 'otherNames': ['Glasses', 'Spectacles'], 'description': 'Children assigned to the intervention group (group 1) will receive orthoptic care, including exams 1-3 (depending on the refractive error) times a year, and glasses, based on accurate determinations of refractive error by retinoscopy in cycloplegia by the study orthoptists at age 12-18 months. The spectacles for the children in this study will be provided by the study via their optician without costs.', 'armGroupLabels': ['Group 1 - High refractive error: Intervention']}, {'name': 'Orthoptic care without the prescription of glasses from age 12-18 months onwards', 'type': 'OTHER', 'description': 'Children with high refractive error in the control group (group 2) will also receive orthoptic care, including exams 1-3 (depending on the refractive error) times a year, but they will not receive glasses.', 'armGroupLabels': ['Group 2 - High refractive error: Control']}, {'name': 'First measurement only', 'type': 'OTHER', 'description': 'Children who have no or mild refractive error (group 3), the majority of all children, will be examined by the study orthoptists only once at the age of 12-18 months, after which youth health care (YHC) physicians and nurses will continue standard vision screening at CHCs, as part of screening for general health disorders and vaccinations. Visual acuity is measured routinely at 42-48 months as part of standard vision screening.', 'armGroupLabels': ['Group 3 - Mild or no refractive error']}]}, 'contactsLocationsModule': {'locations': [{'zip': 'NL3000CA', 'city': 'Rotterdam', 'country': 'Netherlands', 'facility': 'Dept. of Ophthalmology Erasmus Medical Center', 'geoPoint': {'lat': 51.9225, 'lon': 4.47917}}], 'overallOfficials': [{'name': 'Huibert J Simonsz, MD, PhD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Erasmus Medical Center'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Erasmus Medical Center', 'class': 'OTHER'}, 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'Principal Investigator, MD, PhD', 'investigatorFullName': 'Huib Simonsz', 'investigatorAffiliation': 'Erasmus Medical Center'}}}}