Actively Recruiting
Transcranial Electrical Stimulation and the Reading Brain: Toward Novel Interventions for Reading Impairments
Led by Silvia Brem · Updated on 2026-05-22
60
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
S
Silvia Brem
Lead Sponsor
S
Swiss National Science Foundation
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the effects of transcranial electrical stimulation (tES) on the brain to enhance learning related to reading. This study focuses on adults with a range of reading abilities and explores how tES, particularly transcranial random noise stimulation (tRNS), may support learning in developmental dyslexia, a common childhood learning disorder that can persist into adulthood. The study aims to find new treatment techniques beyond standard reading exercises, which often do not fully address the difficulties experienced by individuals with dyslexia. Participants will receive either active tRNS applied to the left superior temporal gyrus using a high-definition electrode setup or a sham stimulation where no electrical current is applied. Both groups perform an artificial orthography learning task, simulating letter-speech sound learning, while undergoing functional magnetic resonance imaging (fMRI). The study includes two sessions: a baseline session and a second session up to eight weeks later. During the study, participants will be assessed using behavioral tests and brain imaging to measure learning performance and brain activity related to reading. The main outcomes include task performance and fMRI activation and connectivity during print processing. Additional cognitive and reading-related measures will also be collected. Participants are involved for up to eight weeks, including brain imaging sessions and stimulation while performing the learning tasks, with safety and brain function monitored throughout.
CONDITIONS
Brief Title
Enhancing Letter-Speech Sound Learning and Reading Network Activation With Transcranial Electrical Stimulation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18-35 years
- All genders
- Written informed consent by the participant
- Native German speaker
- Right-handed
You will not qualify if you...
- Diagnosed neurological disorders, intellectual disabilities, or psychiatric disorders (excluding dyscalculia, ADHD, or Autism Spectrum Disorders)
- History of acquired brain damage or fetal alcohol syndrome
- Uncorrected hearing or vision problems
- Inability to understand or follow instructions in Swiss-German or German
- Current use of psychoactive medications or history of substance abuse affecting brain function or MRI quality
- Nonverbal IQ below 80
- Previous participation in a transcranial electrical stimulation study
- Ability to read or write in a language using non-Latin alphabet letters
- Contraindications to brain stimulation or MRI including epilepsy, severe migraine, skull breaches, neurostimulators, pacemakers, non-MR safe hearing devices, metal implants, claustrophobia, recent surgery, pregnancy, inability to lie still, or non-removable dental braces
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.
1 visit (in-person)
Duration - Up to 8 weeks
Participants receive either active transcranial random noise stimulation or sham stimulation while performing an artificial orthography learning task with simultaneous fMRI scanning.
2 visits (in-person) including baseline and follow-up sessions with fMRI and stimulation
Trial Site Locations
Total: 1 location
1
University Hospital of Psychiatry
Zurich, Switzerland
Actively Recruiting
Research Team
S
Silvia Brem, Prof. Dr.
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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