Actively Recruiting
Viewing Strategy Training in Children With (Cerebral) Visual Impairment: From Spontaneous Eye Movements to a Structured Viewing Strategy
Led by Royal Dutch Visio · Updated on 2026-01-07
60
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
R
Royal Dutch Visio
Lead Sponsor
R
Radboud University, Behavioural Science Institute, Nijmegen, The Netherlands
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying how children with normal vision, ocular visual impairment, and cerebral visual impairment (CVI) use viewing strategies to process visual information. The study aims to understand differences in these strategies among these groups and to evaluate if training can improve how children process visual information. This project addresses a gap in scientific evidence about the effectiveness of viewing strategy training, which is often used in clinical practice but not yet proven. Children in the study receive viewing strategy training lasting six weeks, with sessions twice a week for 30 minutes each. During training, they learn specific ways to look at visual tasks, including structured gaze direction, zooming in and out, and improving visual discrimination. The training follows a set protocol and uses verbal instructions and exercises supported by a textbook documenting children's reactions. The study has two groups: an early training group and a late training group, each with scheduled assessments at baseline, shortly after training, and follow-up periods up to eight months. Participants will be assessed through measures including reading accuracy and speed, visual search accuracy and speed, and eye movement patterns such as saccade amplitude and fixation duration. Additional tests evaluate visual processing speed and selective attention. These assessments occur at multiple time points depending on the group, with follow-ups up to eight months after training. The study includes children aged 5 to 12 years, and researchers will monitor progress to understand how training affects visual processing over time.
CONDITIONS
Brief Title
Viewing Strategy Training in Children With (Cerebral) Visual Impairment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children aged 5 to 12 years
- Typically developing children with normal vision: linear distant visual acuity of 0.1 logMAR or better
- Children with ocular visual impairment: linear distance visual acuity better than 0.1 and up to 1.3 logMAR, intact central visual field greater than 30 degrees
- Children with cerebral visual impairment (CVI): linear distance visual acuity up to 0.3 logMAR, diagnosis verified by ophthalmologists
- Verbal IQ above 70
- No developmental disorders or psychiatric problems like autism spectrum disorder (ASS) or attention deficit/hyperactivity disorder (AD(H)D)
- For training effectiveness evaluation: children aged 5 to 9 years with indication for viewing strategy training and problems in academic task performance
You will not qualify if you...
- Children with visual impairment having linear near visual acuity greater than 1.0 logMAR
- Children with visual field defects less than 30 degrees
- Verbal IQ below 70
- Children who attended vision training in the past two years
- Children with psychiatric problems like autism spectrum disorder (ASS) or attention deficit/hyperactivity disorder (AD(H)D)
- Auditory impairment or language impairments
- Major life events during training
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 6 weeks
Participants receive viewing strategy training consisting of protocol-based verbal instructions and exercises twice a week for six weeks, each session lasting 30 minutes.
2 visits per week for 6 weeks
Duration - Up to 8 months depending on group
Participants have assessments to measure changes in reading and visual search performance after the training, including baseline, posttest, and follow-up measurements depending on group assignment.
3 visits (baseline, posttest within 2 weeks after training, and follow-up at 4 to 8 months)
Trial Site Locations
Total: 1 location
1
Royal Dutch Visio
Nijmegen, Netherlands
Actively Recruiting
Research Team
B
Bianca Huurneman, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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