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Clinical Trial Summary

The present study grounds on the absence of evidence-based treatment in individuals with dyslexia. At this topic, the present study will explore the potential effect of transcranial direct current stimulation (tDCS) over parieto-occipital brain regions, cerebral areas usually disrupted in individuals with dyslexia. tDCS will be administered without concomitantly training. Therefore, the investigators hypothesized that active tDCS over parieto-occipital areas will enhance reading skills in children and adolescents with dyslexia. On the contrary, sham tDCS (placebo) over parieto-occipital areas will not have significant effect on reading. Further, both active and sham tDCS will be safe and well-tolerated.


Clinical Trial Description

The study design is randomized stratified, cross-over, double-blind, placebo-controlled. Children and adolescents with dyslexia will be selected and randomly assigned to two different groups: 1. Active tDCS over parieto-occipital areas + sham tDCS over parieto-occipital areas (Active-Sham tDCS); 2. Sham tDCS over parieto-occipital areas + active tDCS over parieto-occipital areas (Sham-Active tDCS). In this project, the investigators will work to understand whether a brain-based intervention, with the use of tDCS without combined training, can enhance reading in individuals with dyslexia. The protocol will allow the investigators to: 1. Testing the efficacy of stand-alone tDCS in enhancing reading in individuals with dyslexia; 2. Testing the critical role of brain regions (parieto-occipital areas) usually involved in reading and disrupted in dyslexia; 3. Predicting outcomes based on reading-related skills; 4. Investigating the safety and tolerability of tDCS; The overarching goal is to provide a scientific foundation for devising new rehabilitation strategies in dyslexia. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04244578
Study type Interventional
Source Bambino Gesù Hospital and Research Institute
Contact
Status Completed
Phase N/A
Start date May 1, 2016
Completion date February 1, 2021

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