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Clinical Trial Summary

This is a 2-month study in which eligible ADHD adolescents will be provided with personalized VIZO Glasses


Clinical Trial Description

This is a pilot, open-label study of a 2-month treatment with VIZO Glasses. Following the enrollment, the participants will go through an adjustment process where they will be fitted with a personalized pair of VIZO Glasses. The participants will be instructed to wear the glasses throughout the day for two months. A follow-up visit at the end of the 2-month treatment will be conducted to assess the efficacy of VIZO Glasses on managing ADHD symptoms, using the ADHD Rating Scale (ADHD-RS) parent-report questionnaire, the Behavior Rating Inventory of Executive Function (BRIEF), the Conners Continuous Performance Test-3, and the Clinical Global Impression-Improvement (CGI-I). Safety will be monitored by documentation of adverse events. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05835336
Study type Interventional
Source VIZO Specs Ltd
Contact Yael Richter, PhD
Phone +972-54-7384809
Email yaelr@vizo-o.com
Status Recruiting
Phase N/A
Start date April 1, 2022
Completion date September 2023

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