Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
Healthy Volunteers
ID05523505

Bridging the Gap Between Brain Network Science and High-definition Non-invasive Brain Stimulation to Develop a Scalable Adult Literacy Intervention

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

100

Participants Needed

1

Research Sites

N/A

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

This research aims to develop a scalable adult literacy intervention by combining brain network science of resilience to reading disorders with advances in high-definition non-invasive brain stimulation. The study focuses on adults aged 18 to 40 with a range of reading comprehension abilities, addressing the lack of effective treatments for low adult literacy. It investigates how non-invasive brain stimulation affects reading behavior and brain function compared to traditional behavioral interventions, with potential wider impacts on clinical treatments for other disorders. The study involves 100 adults who will participate in three lab visits including behavioral tests, MRI, and EEG assessments. Participants are randomly assigned to one of three stimulation groups: sham stimulation, real stimulation targeting the left angular gyrus, or real stimulation targeting both the left dorsolateral prefrontal cortex and left angular gyrus. All will also receive a standard paper-and-pencil reading comprehension intervention. Brain stimulation sessions occur during MRI and EEG recording to assess immediate and prolonged effects. During participation, individuals will undergo baseline assessments, receive stimulation combined with behavioral testing, and return for follow-up evaluations to measure changes in reading comprehension and brain activity. Researchers will monitor reading comprehension changes on standardized tests over 12 months and brain activation changes during reading tasks. The total involvement includes multiple visits with detailed behavioral and brain imaging measures to evaluate the intervention effects safely and thoroughly.

CONDITIONS

Brief 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
  • Adults aged 18 to 40 years
  • Typical word reading ability (at or above 15th percentile)
  • Range of reading comprehension ability (good or poor)
  • Willingness to participate in three lab visits including behavioral testing, MRI, and EEG
Not Eligible

You will not qualify if you...

  • Personal history of stroke or seizures
  • Taking medications prescribed for stroke or seizures
  • Previous diagnosis of intellectual disability
  • Known uncorrectable visual impairment
  • Documented hearing loss greater than or equal to 25 dB
  • Medical contraindication to MRI (e.g., metal devices)
  • IQ below 70
  • Pervasive developmental disorder
  • Neurologic pathologies such as epilepsy, spina bifida, cerebral palsy, brain tumors, or traumatic brain injury
  • Recent diagnosis of migraines
  • Pregnancy
  • History of syncope
  • Severe fatigue
  • Bilingualism or low English proficiency
  • Poor reading ability preventing task completion
  • Comorbid severe psychiatric disorders
  • Hairstyles preventing proper EEG net fitting or risking EEG net damage

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

3 visits to the lab including behavioral testing, MRI, and EEG

Treatment

Duration - Across 3 visits over the study period

Participants receive non-invasive brain stimulation combined with a behavioral reading comprehension intervention during in-person lab visits.

3 visits to the lab: Visit 1 (baseline measures, 3.5 hours), Visit 2 (stimulation intervention, 3 hours), Visit 3 (follow-up assessment, 2.5 hours)

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

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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