Noninvasive brain stimulation plus augmented reality vision therapy for anisometropic amblyopia in adults
Official title: Combining Noninvasive Brain Stimulation and Augmented Reality-based Dichoptic Therapy for Treating Amblyopic Adults
Run by Polytechnic Institute of Porto · NCT07752433 · Data updated 2026-11-12
This trial tests whether adding HD-tDCS to AR-based dichoptic therapy can improve vision in adults with anisometropic amblyopia.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 40 Years |
| Sex | All |
| Enrollment | 80 (estimated) |
| Sponsor | Polytechnic Institute of Porto Academic / other |
| Locations | 2 sites (Coimbra, Coimbra District and 1 other locations) |
| Status | Recruiting |
| Started | May 1, 2025 |
| Main results expected | December 31, 2027 |
| Study ends | April 30, 2028 |
| Registry record updated | September 18, 2026 |
| Trial ID | NCT07752433 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–40 with unilateral anisometropic amblyopia and at least a 2-line interocular difference in best-corrected visual acuity (worse eye worse than 20/32).
✕Probably not a fit
Individuals with non-anisometropic amblyopia, bilateral amblyopia, or other contraindicating ocular/neuro conditions may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized, double-blind, sham-controlled trial investigates whether combining high-definition transcranial direct current stimulation with augmented reality–based dichoptic therapy improves visual function in adults aged 18–40 with unilateral anisometropic amblyopia. All participants receive the same AR therapy for 10 weeks; during the first 2 weeks they also receive either active or sham HD-tDCS. Primary outcomes include best-corrected visual acuity and depth perception, with secondary measures of contrast sensitivity, interocular suppression, and retinal/visual cortex function. The study leverages individualized contrast adjustments to rebalance binocular input and aims to assess potential neuroplastic gains in adult amblyopia. Enrollment is limited to adults meeting specific anisometropic amblyopia criteria and exclusions to minimize safety risks.
Why it matters
Potential benefit: If successful, participants may experience improved vision in the weaker eye and better depth perception through a noninvasive, AR-based therapy approach.
How similar studies have gone: Prior work suggests that visual training plus noninvasive brain stimulation can induce short-term gains in adult amblyopia, but results vary and this combination with AR dichoptic therapy is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age between 18 and 40 years. * Diagnosis of anisometropic amblyopia. * Unilateral amblyopia with an interocular difference of at least 2 lines in best-corrected visual acuity, with visual acuity worse than 20/32 in the worse-seeing eye. Exclusion Criteria: * Any type of amblyopia other than anisometropic amblyopia. * Bilateral amblyopia. * Ophthalmological or neuro-ophthalmological disease other than amblyopia. * Neurological disease. * Chronic pharmacological treatment. * Presence of an implanted medical device. * Any ocular surgery or treatment within the previous year. * Significant ocular media opacities. * Previous treatment with transcranial direct current stimulation or another non-invasive brain stimulation technique. * Pregnancy or planning to become pregnant during the study period. * Inability to provide informed consent. * History of head trauma, seizures, or frequent headaches. * Electrical or electronic implants, such as a cardiac pacemaker. * Metallic objects or implants in the head, except dental implants.
Where it's running
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Coimbra Institute for Biomedical Imaging and Translational Research (CIBIT), University of Coimbra
Coimbra, Coimbra District, Portugal Recruiting -
RISE-Health, Center for Translational Health and Medical Biotechnology Research (TBIO), School of Health, Polytechnic of Porto
Porto, Porto District, Portugal Recruiting
Study contacts
- Study coordinator: Catarina A Mateus, PhD
- Email: cms@ess.ipp.pt
- Phone: +351 913474780
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Augmented Reality Binocular Therapy for Adult Amblyopia
This trial tests a home-based augmented reality binocular therapy to see if it improves vision in adults 18–40 with anisometropic amblyopia, compared with placebo training.
-
Psilocybin-assisted therapy to help adults with amblyopia see more clearly
This study tests whether a single or small doses of psilocybin can boost the effectiveness of amblyopia treatment in adults.
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Gabor-based visual training for adults with amblyopia
This study tests a computer-based Gabor training program to see if it can improve vision in adults aged 18–39 with amblyopia due to anisometropia or strabismus.
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tDCS for paediatric amblyopia
This study tests whether non-invasive brain stimulation (tDCS) can improve vision for children aged 4–14 with amblyopia who didn’t get enough help from patching.
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Gamified visual training with occlusion for kids with anisometropic amblyopia
This trial tests two kid-friendly digital games plus patching to see if they improve vision and motivation in children aged 4–7 with anisometropic amblyopia compared with patching alone.
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Combined fluoxetine and patching to improve and maintain vision in amblyopia using OCTA and VEP
This project will test whether adding fluoxetine to standard eye patching helps improve and maintain vision in people over 10 with amblyopia.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.