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Clinical Trials/NCT05583136
NCT05583136
Completed
Not Applicable

Restoring Neural Oscillatory Communication Between Dorsal and Ventral Visual Streams in Developmental Dyslexia

IRCCS Ospedale San Raffaele1 site in 1 country78 target enrollmentDecember 14, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Developmental Dyslexia
Sponsor
IRCCS Ospedale San Raffaele
Enrollment
78
Locations
1
Primary Endpoint
Reading score
Status
Completed
Last Updated
last year

Overview

Brief Summary

Developmental dyslexia (DD) is a multifactorial disorder that hampers the education of about 10% of individuals across cultures and is associated to both phonological and visual deficits. The latter have been linked to a deficit in the magnocellular-dorsal (M-D) visual stream, that has a critical role in guiding the activity of ventral visual stream areas where letters identity is extracted. Here, we will test the efficacy of transcranial alternate current stimulation (tACS) of the M-D stream combined with reading trainings in adult participants with DD, assessing the neurophysiological underpinnings of these new trainings with EEG and fMRI/DTI.

Registry
clinicaltrials.gov
Start Date
December 14, 2021
End Date
December 23, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Luca Ronconi

Professor

IRCCS Ospedale San Raffaele

Eligibility Criteria

Inclusion Criteria

  • Adult patient (age between 18 and 35)
  • Official Diagnosis of Developmental Dyslexia (DD)
  • Normal or corrected-to-normal vision and hearing
  • Normal motor skills

Exclusion Criteria

  • Participants that cannot sign the consent form
  • Participants unable to read or understand and correctly complete the procedures foreseen by the study
  • Participants with a diagnosis or personal history of epilepsy or patients with a positive family history of epilepsy
  • Pregnant or breastfeeding patients
  • Participants with major psychiatric or neurological disorders and/or currently in psychopharmacological treatments.
  • Participants with metal implants in the brain, pacemakers, brain stimulators, cochlear implants.
  • Participants with claustrophobia (only for fMRI)

Outcomes

Primary Outcomes

Reading score

Time Frame: Pre-training, 1-7 days post-training, follow-up at 1 and 6 months

Text, word and pseudowords reading score

Study Sites (1)

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