Clinical trial Recruiting at 2 sites Interventional Ages 18 to 40

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 typeInterventional
Ages18 Years to 40 Years
SexAll
Enrollment80 (estimated)
SponsorPolytechnic Institute of Porto
Academic / other
Locations2 sites (Coimbra, Coimbra District and 1 other locations)
StatusRecruiting
StartedMay 1, 2025
Main results expectedDecember 31, 2027
Study endsApril 30, 2028
Registry record updatedSeptember 18, 2026
Trial IDNCT07752433 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

  • 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.