Actively Recruiting
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
Eligibility Criteria
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
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
Complete this quick 3-step screening to check your eligibility
Your Study Journey
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
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
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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