Recruiting

A-tDCS & Perceptual Learning

Sponsor:

University of Waterloo

Code:

NCT04762368

Conditions

Macular Degeneration

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Active anodal tDCS

Sham anodal tDCS

Study Details

Brief summary:

The purpose of this study is to test whether a kind of brain stimulation called anodal transcranial direct current stimulation (a-tDCS) can be combined with perceptual learning to improve the ability of people with age-related macular degeneration (AMD) or juvenile macular degeneration (JMD) to read words presented to them on a computer screen better than if perceptual learning alone were used.

In addition, secondary measures of visual acuity will also be examined to determine whether brain stimulation can allow patients to resolve finer details of an image. The proposed treatment is the application of a-tDCS onto the participant's head, with brain stimulation aimed at Primary Visual Cortex toward the occipital pole, while patients undergo six separate sessions of training. The investigators will test the ability of participants to read words before the start of the training sessions (pre test) and after the completion of all training sessions (post test). This is a between-subjects design, and half of the participants will receive true stimulation, and the other half will receive sham stimulation. The difference between the pre and post tests when receiving active stimulation will be compared to the difference when receiving sham stimulation, because the sham stimulation is not expected to influence reading beyond a placebo. The aim of the study is to examine the potential of concurrent brain stimulation and perceptual learning as an effective treatment for macular degeneration that may be used in conjunction with more traditional eye-based interventions. The investigators hypothesize that the brain stimulation will enable higher performance in the reading task after and secondary measures after perceptual training due to an increase in the cortical excitability of the stimulated brain cells.

Conditions

Macular Degeneration

Study ID

NCT04762368

Start date

Feb 13, 2021

Status verified date

May, 2025

Completion date

Dec, 2026

Anticipated

Primary completion date

Dec, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Diagnosis of AMD (age 60+) or JMD (current age 18+).
2. Visual acuity (VA); between 6/9-6/96 in the better eye
3. Best-corrected near visual acuity of 4.0M at 40 cm or better in the better eye
4. Stable vision in previous 3 months (patient report)
5. Central vision loss

Exclusion Criteria:

1. Diagnosed dementia.
2. Not fluent in reading English (Waterloo) or Chinese characters (Hong Kong).
3. Any ocular surgery (including anti-vegF injections) within the duration of the study, except for: A. Chronic and continuous injections for at least 1 year. B. Injections stopped at least 2 months before participation. C. Injections in the untested eye
4. Ocular pathology other than JMD or AMD that can significantly reduce central vision. Example: mild cataract of grade 2 or below is acceptable
5. Severe hearing impairment.
6. Contraindications for brain stimulation

Study Design

Enrollment

30 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

active comparator: Active + Training

Participants in this arm will be exposed to active stimulation for the first 25 minutes of a roughly hour - long perceptual training procedure in which participants must verbally read sentences presented at various speeds and sizes.

sham comparator: Sham + Training

Participants in this arm will be exposed to sham stimulation for the first 25 minutes of a roughly hour - long perceptual training procedure in which participants must verbally read sentences presented at various speeds and sizes.

Interventions

Active anodal tDCS

a weak electric current is applied to the head through electrodes to affect the cortical excitability of the targeted cells in the brain.

Sham anodal tDCS

The tDCS machine will be used as in active stimulation, except the electrical current will not be applied.

Primary outcome measure

  • Change in Rapid Serial Visual Presentation (RSVP) Reading performance before and right after training. [ Time Frame: The pre test and post test will take roughly 1 hour to complete, and they will be roughly 4-7 weeks apart. ]
  • Change in Rapid Serial Visual Presentation (RSVP) Reading performance 30 days after training [ Time Frame: The test will take roughly 1 hour to complete, and they will be roughly 7-10 weeks apart. ]

Central Contacts and Locations

Central contacts

Locations

University of Waterloo

Recruiting

Waterloo, Ontario, Canada, N2L 3G1

Contacts

Andrew E Silva, PhD

a8silva@uwaterloo.ca

More Information

Sponsor

University of Waterloo

Last update posted

Jan 22, 2026

Last verified

May, 2025

Keywords

  • Macular Degeneration
  • Brain Stimulation
  • Psychophysics
  • Reading
  • tDCS
  • RSVP
  • Visual Acuity
  • Uncrowded Visual Acuity
  • Crowded Visual Acuity
  • Contrast Sensitivity

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Waterloo on 2026-01-22.