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Visual Perceptual Learning for the Treatment of Visual Field Defect

Visual Perceptual Learning for the Treatment of Visual Field Defect

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01959256
Acronym
VIVID
Enrollment
36
Registered
2013-10-09
Start date
2013-10-31
Completion date
2018-01-31
Last updated
2019-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke, Visual Field Defect

Keywords

Stroke, Visual Field Defect, Visual perceptual learning, Brain connectivity

Brief summary

This study will test the hypothesis whether visual field defect caused by chronic stroke could be improved by visual perceptual learning. The secondary hypothesis is that improvement of visual field defect would be accompanied by connectivity changes in visual networks. In addition, investigators will evaluate whether improvement of visual field defect could achieve improvement of subjective visual function.

Detailed description

Study design: A PROBE (Prospective, Randomized, Open-label, Blinded-endpoint) design Methods: 1. Visual perceptual learning (VPL) group 1. Visual perceptual learning (24 times for 2 months, 3 times per week) in visual field defect areas 2. At baseline and post-VPL evaluations (2 months after): Structural & Functional MRIs, Visual field tests, Visual evoked potential, Visual cognitive tests, Subjective visual function questionnaires 2. Control group 1. At baseline and 2-months later: No VPL, Structural & Functional MRIs, Visual field tests, Visual evoked potential, Visual cognitive tests, Subjective visual function questionnaires 2. Visual perceptual learning after 2-month follow-up evaluation (24 times for 2 months, 3 times per week) (The patients who were stratified by age (over 65 years old or not) and degree of visual field defect (quadrantanopia or complete hemianopia) will be randomly assigned into the learning and control group.) 3. Investigations 1. Improvement of visual field test scores between VPL group and control group 2. Analysis of brain network changes in MRI data 3. Correlation analysis of improvement of visual field defect and MRI data 4. Correlation analysis of improvement of visual field defect and visual evoked potential (VEP) data 5. Correlation analysis of improvement of visual field defect and neuropsychological data

Interventions

24 times of training for visual perceptual learning

Sponsors

Asan Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. The patient has chronic stroke more than 6 months after onset. 2. The patient has visual field defect (Quadrantanopia or Hemianopia). 3. The patient has corrected eyesight 0.7 or above.

Exclusion criteria

1. The patient has contraindication to MRI scan. 2. The patient has cognitive impairment (Mini-Mental Status Exam score \<24). 3. The patient has ophthalmologic diseases (e.g., glaucoma, cataract).

Design outcomes

Primary

MeasureTime frameDescription
Improvement of visual field scores in visual field defect areasAt 2 months (plus or minus 7 days) after baseline evaluationImprovement of mean deviation scores in defected areas by Humphrey 750i Field test

Secondary

MeasureTime frameDescription
Performance of visual perceptual learningAt 2 months (plus or minus 7 days) after baseline evaulationPerformance (scores) of visual perceptual learning
Connectivity changes in MRIBetween baseline and 2 months (plus or minus 7 days) after1. Functional connectivity changes in resting-state functional MRI 2. Structural connectivity changes in diffusion tensor imaging
Improvement of visual field score in whole visual field areaAt 2 months (plus or minus 7days) after baseline evaluationImprovement of mean deviation scores in whole visual field by Humphrey 750i Field test
Change of subjective visual functionAt 2 months (plus or minus 7days) after baseline evaluation1. Change in Korean version of National Eye institute Visual Functioning Questionnaire-25 (NEI-VFQ-25) 2. Change of subjective visual field area
Changes of visual evoked potentialBetween baseline and 2 months (plus or minus 7 days) afterChanges between baseline and 2 months after in half-field visual evoked potential (VEP) data

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026