Biofeedback training for children with idiopathic infantile nystagmus

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of biofeedback training (BT) for children diagnosed with idiopathic infantile nystagmus (IIN), a condition that affects eye movement and vision. The approach involves using advanced microperimetry instruments to provide real-time feedback during eye movement control training. The goal is to systematically assess the impact of BT on visual acuity and eye movement stability in affected children, ultimately formulating guidelines for its clinical application. Traditional therapies have focused on surgical and optical interventions, making this a novel approach in low vision rehabilitation.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Diagnosed as Infantile idiopathic nystagmus (IIN)
* Ability to follow the visual and auditory stimuli and training instructions

Exclusion Criteria:

* Ocular diseases not related to the nystagmus physiopathology
* Both eyes with media opacity that impairs microperimetry testing
* Peripheral nystagmus cases
* Other types of nystagmus than IIN
* Inability to perform during testing and training

Where it's running

• Cnib
  Toronto, Ontario, Canada Recruiting

Study contacts

• Principal investigator: Samuel Markowitz, MD — University of Toronto
• Study coordinator: Monica Daibert-Nido, MD
• Email: monica.nido@uhn.com
• Phone: 4164819995

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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.