Enhancing Letter-Speech Sound Learning With Non-Invasive Brain Stimulation
Official title: Transcranial Electrical Stimulation and the Reading Brain: Toward Novel Interventions for Reading Impairments
Run by Psychiatric University Hospital, Zurich · NCT07546292 · Data updated 2026-11-12
Researchers test whether transcranial random noise stimulation (tRNS) helps adults learn letter-sound mappings for reading.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 35 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Psychiatric University Hospital, Zurich Academic / other |
| Locations | 1 site (Zurich) |
| Status | Recruiting |
| Started | April 23, 2026 |
| Main results expected | June 2027 |
| Study ends | June 2027 |
| Registry record updated | May 22, 2026 |
| Trial ID | NCT07546292 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18-35 who are German-speaking, right-handed, and able to consent.
✕Probably not a fit
Individuals with certain neurological, psychiatric, or sensory exclusions, or those who do not meet language and handedness criteria, may not experience benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This trial tests if non-invasive brain stimulation can boost learning related to reading in adults with varied reading abilities. Participants receive transcranial random noise stimulation while performing an artificial orthography learning task, which mimics the process of linking letters with sounds. The study uses behavioral tests and functional MRI to examine learning outcomes and brain activity. The goal is to understand whether tRNS can support reading-related learning and its neural mechanisms, potentially informing future interventions for dyslexia. The research is conducted at a Swiss institution with a focus on translational insights for developmental dyslexia across ages.
Why it matters
Potential benefit: If successful, this approach could lead to new non-invasive methods to support reading learning in individuals with dyslexia or reading difficulties.
How similar studies have gone: Previous tES studies have shown mixed but promising behavioral and neural effects on learning and reading-related tasks.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 18-35 * All genders * Written informed consent by the participant * German speaking (native) * Right-handed Exclusion Criteria: * Diagnoses of neurological disorders, intellectual disabilities, or psychiatric disorders (We do not exclude participants with common comorbidities of dyslexia, specifically dyscalculia, Attention Deficit/Hyperactivity Disorder, or Autism Spectrum Disorders) * History of any acquired brain damage or evidence of fetal alcohol syndrome * Hearing problems and vision problems that cannot be corrected * Inability to follow procedures or understand the instructions given in (Swiss-)German * Current use of psychoactive medications or substances, or a history of substance abuse that may affect brain function, performance or MRI signal quality * A nonverbal IQ \< 80 * Having previously participated in a transcranial electrical stimulation study * Knowledge to read or write in a language using foreign letters (i.e., different from the Latin alphabet) * Contraindications to brain stimulation or MRI, such as: History of epilepsy or severe migraine; Skull breach such as craniotomy; Wearing neurostimulators or cardiac pacemakers; Wearing hearing aid devices or cochlear implants, which are not MR safe; Having metal pieces in their body (e.g., piercings that cannot be removed and contain metal, screws or plates from surgical operations, wounds from metal splinters or similar); Claustrophobia or problems lying in the scanner (e.g., pain, anxiety); Previous surgery on the head or heart; Being pregnant (a pregnancy test will be conducted at the MR center before the measurement if a female participant suspects she might be pregnant or is uncertain about her pregnancy status according to the Swiss Ethics Leitlinie: https://swissethics.ch/assets/pos\_papiere\_leitfaden/20110906\_kek\_mri.pdf); Having problems lying still (strong cold, tremor, etc.); Wearing non-removable dental braces
Where it's running
-
University Hospital of Psychiatry
Zurich, Switzerland Recruiting
Study contacts
- Study coordinator: Silvia Brem, Prof. Dr.
- Email: silvia.brem@kjpd.uzh.ch
- Phone: +41 (0)58 384 67 11
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.