Actively Recruiting
Characterization of Multiple Factors in Training and Plasticity in Central Vision Loss: Macular Degeneration
Led by University of Alabama at Birmingham · Updated on 2026-02-09
60
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Alabama at Birmingham
Lead Sponsor
U
University of California, Riverside
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying how the brain adapts and changes after central vision loss, focusing on macular degeneration (MD), a common cause of vision loss that affects central vision. This research aims to better understand how different visual processes and brain systems work together to improve daily vision tasks such as reading, navigation, and face recognition. The study compares perceptual learning (PL) in people with natural and simulated central vision loss to explore brain plasticity and its effects on vision rehabilitation. The study evaluates two training approaches for improving vision in people with MD. One approach trains early visual processing by teaching participants to distinguish orientations of specific visual patterns (Gabor patches) at very low contrast levels. The other combines training in visual sensitivity, spatial integration, and attention to eye movements. These trainings are delivered over approximately seven weeks, with effects measured shortly after training completion. Participants will undergo assessments before and after training, including tests measuring changes in visual crowding, eye movement precision, and fixation stability. Eye-tracking and psychophysical tests will evaluate how training affects vision and brain activity. The study also involves reviewing medical records and visual sensitivity tests to confirm eligibility. Researchers will monitor participants' progress, aiming to understand how vision training can support brain plasticity and improve vision-related functions in people with MD.
CONDITIONS
Brief Title
Factors in Learning And Plasticity: Macular Degeneration
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18-89 years
- Severely impaired vision in both eyes (20/100 or worse)
- Diagnosis of Macular Degeneration by an Ophthalmologist
- Light sensitivity in the macular retina at least 10 dB worse than peripheral regions demonstrated by scanning laser ophthalmoscope (MAIA)
- Medical record indicating this severity has been present for at least 2 years
- Reside within 50 miles of the study site
You will not qualify if you...
- Pacemaker or any ferromagnetic metal implanted in the body
- Any metal implanted in the head (limited dental work is acceptable)
- Claustrophobia
- Hearing impairment
- Weight over 300 pounds
- Maximum body girth over 60 inches
- Previous serious head injury
- Presence of hallucinations or delusions
- Excessive old or colorful tattoos near the head
- Pregnancy
- Braces or permanent retainer
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 - Approximately 7 weeks
Participants undergo behavioral training to improve visual processing through either training visual sensitivity or combination training involving multiple visual tasks.
Daily training sessions during the treatment period
Duration - Up to 3 weeks after treatment completion
Participants are assessed for changes in visual performance measures including radial bias, saccadic precision, and fixation stability within 3 weeks after completing training.
1 to 2 follow-up visits
Trial Site Locations
Total: 1 location
1
UAB
Birmingham, Alabama, United States, 35294
Actively Recruiting
Research Team
R
Rachel A Chua, MS
K
Kristina M Visscher, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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