Vision Disorders Clinical Trial
Official title:
Viewing Strategy Training in Children With (Cerebral) Visual Impairment: From Spontaneous Eye Movements to a Structured Viewing Strategy
Viewing strategies are strategies used to process visual Information. Many children with visual impairment seem to lack systematic viewing strategies. However, it is unknown how viewing strategies differ between children with normal vision and children with (cerebral) visual impairment. In addition, viewing strategy training is often adopted in clinical practice, but till date there is no scientific evidence about effectiveness of this approach. The current project has two goals: (1) to measure viewing strategies used by children with normal vision, children with ocular visual impairment and children with CVI, and (2) to evaluate whether training viewing strategies results in more efficiënt visual Information processing.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | September 2026 |
Est. primary completion date | June 2026 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 5 Years to 12 Years |
Eligibility | Inclusion criteria typically developing children with normal vision: - Age 5-12 years - linear distant visual acuity of 0.1 logMAR or better - Verbal IQ above 70 - Absence of developmental disorders or psychiatric problems like ASS or AD(H)D Inclusion criteria for children with ocular visual impairment: - Age 5-12 years - Children with linear distance visual acuity better <=1.3logMAR and >0.1 logMAR - Intact central visual field (at least > 30 degrees) - Children with a verbal IQ above 70 - Absence of developmental disorders or psychiatric problems like ASS or AD(H)D Inclusion criteria for children with cerebral visual impairment: - Age 5-12 years - Linear distance visual acuity <=0.3 logMAR - Having the diagnosis CVI (verified by ophthalmologists) - Children with a verbal IQ above 70 - Absence of psychiatric problems like ASS or AD(H)D Additional inclusion criterion for study 2 (evaluating training effectiveness): children with (cerebral) visual impairment should have an indication for viewing strategy training. Training should not be indicated if children have no problems performing academic tasks (i.e. when speed and accuracy of visual processing is within the normal range). The age range for study 2 is 5-9 years. Exclusion criteria: - Children with VI: linear near visual acuity >1.0 logMAR - Children with visual field defect < 30 degrees - Children with a verbal IQ below 70 - Children who attended a form of vision training in the past two years - Children with psychiatric problems like ASS or AD(H)D - Auditory impairment or language impairments - Major life events during training |
Country | Name | City | State |
---|---|---|---|
Netherlands | Royal Dutch Visio | Nijmegen |
Lead Sponsor | Collaborator |
---|---|
Royal Dutch Visio | Radboud University, Behavioural Science Institute, Nijmegen, The Netherlands |
Netherlands,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in reading accuracy after viewing strategy training | Radner reading test | Group A: Day 0, Month 2, Month 8; group B: Day 0, Month 2, Month 4 | |
Primary | Changes in reading speed after viewing strategy training | Radner reading test | Group A: Day 0, Month 2, Month 8; group B: Day 0, Month 2, Month 4 | |
Primary | Changes in visual search accuracy after training | Accuracy during conjunction search | Group A: Day 0, Month 2, Month 8; group B: Day 0, Month 2, Month 4 | |
Primary | Changes in visual search speed after training | Speed during conjunction search | Group A: Day 0, Month 2, Month 8; Group B: Day 0, Month 2, Month 4 | |
Primary | Changes in saccade amplitudes during reading and visual search after training | Saccade amplitudes measured using Radner reading test and conjunction search | Group A: Day 0, Month 2, Month 8; Group B: Day 0, Month 2, Month 4 | |
Primary | Changes in fixation duration during reading and search after training | Fixation durations measured using Radner reading test and conjunction search | Group A: Day 0, Month 2, Month 8; Group B: Day 0, Month 2, Month 4 | |
Primary | Changes in average distance between fixation points during conjunction search (EB-VSA) after training | Average distance between fixation points using Radner reading test and conjunction search | Group A: Day 0, Month 2, Month 8; Group B: Day 0, Month 2, Month 4 | |
Secondary | Changes in WISC-V visual processing speed index (VSI) after training | WISC-IV visual processing speed index | Group A: Day 0, Month 2, Month 8; Group B: Day 0, Month 2, Month 4 | |
Secondary | Changes in local visual selective attention after training | TEA-Ch Speurtocht (total number of symbols found in 1 minute) | Group A: Day 0, Month 2, Month 8; Group B: Day 0, Month 2, Month 4 | |
Secondary | Changes in global visual selective attention after training | Gestalt Closure (Kaufman-ABC), number of correct answers | Group A: Day 0, Month 2, Month 8; Group B: Day 0, Month 2, Month 4 | |
Secondary | Changes in visual identification speed after training | 'DST-Plaatjes Benoemen', number of pictures correctly named within 1 minute | Group A: Day 0, Month 2, Month 8; Group B: Day 0, Month 2, Month 4 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT03872479 -
Single Ascending Dose Study in Participants With LCA10
|
Phase 1/Phase 2 | |
Active, not recruiting |
NCT02595502 -
Clinical Evaluation of Two Silicone Hydrogel Daily Disposable Contact Lenses
|
N/A | |
Completed |
NCT02485054 -
A Predictive Score for the Ischemic Etiology of a Transient Visual Disturbances (VASCO)
|
||
Completed |
NCT00985231 -
Performance Evaluation of Contact Lenses Among a Population of Adapted Contact Lens Wearers
|
N/A | |
Recruiting |
NCT05208658 -
Characteristics of the Vergence Responses of Binocularly Normal Subjects After a Vision Therapy Protocol
|
N/A | |
Recruiting |
NCT06077682 -
Cycloplegic Refraction in Pediatric Patients With Esotropia
|
Phase 4 | |
Active, not recruiting |
NCT04123626 -
A Study to Evaluate the Safety and Tolerability of QR-1123 in Subjects With Autosomal Dominant Retinitis Pigmentosa Due to the P23H Mutation in the RHO Gene
|
Phase 1/Phase 2 | |
Recruiting |
NCT04693247 -
Handheld Device Compared With a Standard Eye Care Diagnostic Device in Measuring Ophthalmic Refraction
|
N/A | |
Recruiting |
NCT06451172 -
Novel Antisense Oligonucleotide Eye Drops for Treating Antibiotic-Resistant Bacterial Keratitis
|
Early Phase 1 | |
Completed |
NCT01318577 -
Study of A New Contact Lens Cleaning and Disinfecting Solution
|
N/A | |
Completed |
NCT03763721 -
The ADVISE Study: Advanced Visualization In Corneal Surgery Evaluation
|
N/A | |
Completed |
NCT05602402 -
To Evaluate the Efficacy and Safety of CAEP-01 on Eye Strain in Children With Heavy Screen Use
|
N/A | |
Not yet recruiting |
NCT06085430 -
Kubota Glass Parameter Refinement Study
|
N/A | |
Completed |
NCT04347564 -
Usability of the Software MacuFix for the Categorization of Metamorphopsia
|
||
Completed |
NCT01546402 -
Intraoperative Dexamethasone Implant Improves Outcome of Cataract Surgery With Diabetic Macular Edema
|
Phase 4 | |
Completed |
NCT01698788 -
Effect of Intraoperative Dexamethasone Implant in Taut Posterior Hyaloid Removal in Diabetic Macular Edema
|
N/A | |
Completed |
NCT03169855 -
Validation of Mesopic and Photopic Contrast Vision Tests With Respect to Nighttime Driving Ability
|
||
Terminated |
NCT03913130 -
Extension Study to Study PQ-110-001 (NCT03140969)
|
Phase 1/Phase 2 | |
Recruiting |
NCT03479021 -
SPOT Vision Screening
|
||
Completed |
NCT03780257 -
Study to Evaluate Safety and Tolerability of QR-421a in Subjects With RP Due to Mutations in Exon 13 of the USH2A Gene
|
Phase 1/Phase 2 |