Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
Healthy Volunteers
NCT05523505

Noninvasive Brain Stimulation to Enhance Reading Comprehension Ability in Adults

Led by Vanderbilt University · Updated on 2025-08-01

100

Participants Needed

1

Research Sites

200 weeks

Total Duration

On this page

Sponsors

V

Vanderbilt University

Lead Sponsor

N

National Institutes of Health (NIH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this project is to address the urgent need for effective, scalable adult literacy interventions by integrating breakthroughs in two separate fields: 1.) the brain network science of resilience to reading disorders and 2.) high-definition non-invasive brain network stimulation. This study will first establish the efficacy of a novel, noninvasive stimulation protocol on reading behavior and brain metrics; then will determine how stimulation-induced effects interact with baseline reading comprehension ability; and lastly, will identify whether stimulation-induced effects are more clinically-beneficial than canonical behavioral interventions. Results may change the foundation for how we treat low adult literacy, and have the potential for wider reaching impacts on non-invasive stimulation protocols for other clinical disorders.

CONDITIONS

Official Title

Noninvasive Brain Stimulation to Enhance Reading Comprehension Ability in Adults

Who Can Participate

Age: 18Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Right-handed, native English monolingual speakers
  • Age between 18 and 40 years
  • Typical word reading ability at or above the 15th percentile
  • Reading comprehension ability either above 25th percentile (good) or at or below 25th percentile (poor)
Not Eligible

You will not qualify if you...

  • Personal medical history of stroke or seizures
  • Use of medications specifically prescribed for stroke or seizures treatment
  • Previous diagnosis of intellectual disability
  • Uncorrectable visual impairment
  • Hearing impairment of 25 dB or greater
  • Medical contraindications to MRI
  • Known IQ below 70
  • Pervasive developmental disorders
  • Neurologic pathologies including epilepsy, spina bifida, cerebral palsy, traumatic brain injury, brain tumors
  • Recent diagnosis of migraines
  • Pregnancy
  • History of syncope
  • Severe fatigue
  • Bilingualism or low English proficiency
  • Poor reading ability preventing task completion
  • Severe psychiatric disorders
  • Hair styles preventing proper EEG net fitting or posing risk to EEG net

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Vanderbilt University Medical Center

Nashville, Tennessee, United States, 37203

Actively Recruiting

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Research Team

T

Tess Fotidzis, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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