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RecruitingNCT07546292LexiStimUpdated May 22, 2026

Enhancing Letter-Speech Sound Learning and Reading Network Activation With Transcranial Electrical Stimulation

An interventional study of Transcranial random noise stimulation and Sham Stimulation in Dyslexia, Developmental, Reading and Dyslexia, sponsored by Silvia Brem. Recruiting at 1 site in Switzerland. Open to participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-22.

Sponsored by Silvia Brem · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

This study investigates the effects of transcranial electrical stimulation (tES) on the brain and its potential to enhance reading-related learning. Adult participants with a range of reading abilities will receive transcranial random noise stimulation (tRNS) while they perform an artificial orthography learning task. This task simulates letter-speech sound learning, an important first step during reading acquisition known to be impaired in individuals with developmental dyslexia. The effects of the intervention will be assessed using both behavioral measures and functional magnetic resonance imaging (fMRI).

Read the detailed description

This study investigates the effects of transcranial electrical stimulation (tES) on the brain and its potential to enhance reading-related learning. The aim is to identify novel techniques for treating developmental dyslexia, which is a common learning disorder that occurs in childhood and can persist into adulthood. Typically, standard therapy for dyslexia consists of specific reading exercises; however, such training often does not fully remediate the difficulties.

This study, therefore, evaluates how transcranial electrical stimulation may be applied to support learning and ultimately reading. During the stimulation, participants perform an artificial orthography learning task simulating letter-speech sound learning. Whereas previous tES reading studies have focused primarily on behavioral outcomes, the present study additionally measures brain activity using fMRI to elucidate how tES affects neural processing and how these effects may relate to reading abilities.

The knowledge gained from this project is intended to support the future development of transcranial electrical stimulation as an intervention for adults and children with developmental dyslexia.

02

Conditions studied

  • Dyslexia, Developmental
  • Reading
  • Dyslexia
  • Learning
  • Learning Disabilities

Keywords

  • Dyslexia
  • tRNS
  • transcranial electrical stimulation
  • non-invasive brain stimulation
  • neuromodulation
  • reading
  • functional magnetic resonance imaging
  • fMRI
  • audiovisual-learning
03

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Age 18-35
  • All genders
  • Written informed consent by the participant
  • German speaking (native)
  • Right-handed

Exclusion criteria

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

04

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Real Stimulation

    Participants will receive transcranial random noise stimulation (tRNS) applied to the left superior temporal gyrus.

    Other: Transcranial random noise stimulation

  • Sham comparator
    Sham Stimulation

    Participants in this group will serve as the control condition. The setup will be identical to the active stimulation group, but stimulation will be sham, such that no electrical current will be applied for the duration of the session.

    Other: Sham Stimulation

Interventions

  • OtherTranscranial random noise stimulation

    Participants will receive high-frequency tRNS (max. 1.5 mA) applied to the left superior temporal gyrus. A high-definition setup (3x1 electrodes) will be used to achieve more focal stimulation. Stimulation will be applied during an artificial orthography learning task with simultaneous fMRI acquisition.

  • OtherSham Stimulation

    Participants will also have electrodes placed on their scalp. The setup is programmed to induce a short ramp-up of the chosen electrical current followed by a ramp-down at the beginning and at the end of the stimulation. In between, no current will be applied. Sham stimulation will be applied during an artificial orthography learning task with simultaneous fMRI acquisition.

05

What researchers measure

Primary outcomes

  1. Performance in the artificial orthography learning task

    Performance on the artificial orthography learning task and the artificial orthography reading fluency test will be compared between the stimulation and sham groups.

    Time frame: At second session, up to 8 weeks after baseline

  2. fMRI activation and connectivity during print processing

    fMRI activation and connectivity of the posterior superior temporal gyrus and other regions of the reading and audiovisual learning networks will be compared before, during and after transcranial electrical stimulation (tES). The fMRI tasks performed in the second session include artificial orthography learning and explicit print processing (lexical decision task), whereas implicit print processing (one-back task) is performed both at baseline and in the second session. These changes in activation and connectivity will be compared between the stimulation group and the sham group.

    Time frame: At baseline (Session 1) and at second session, up to 8 weeks after baseline

Secondary outcomes

  1. fMRI brain activation and connectivity in further fMRI tasks: audiovisual processing and naturalistic movie watching

    Brain activation and connectivity during further fMRI tasks, namely an audiovisual localizer task and a movie-watching paradigm, will be investigated and compared between the two groups. The audiovisual localizer task focuses on brain activation in reading and audiovisual processing regions, and the movie-watching paradigm on connectivity within the resting-state networks.

    Time frame: At baseline (Session 1) and at second session, up to 8 weeks after baseline

  2. Reading and reading-related behavioral measures

    Reading and reading-related tasks, such as word and pseudoword reading, will be performed before and after tES to provide a behavioral estimate of reading skills.

    Time frame: At baseline (Session 1) and at second session, up to 8 weeks after baseline

  3. Performance in further cognitive tasks

    The performance in further cognitive tasks (working memory, attention, rapid automatized naming) will be compared before and after tES.

    Time frame: At baseline (Session 1) and at second session, up to 8 weeks after baseline

06

Study locations

1 of 1 sites recruiting
  • University Hospital of Psychiatry
    Zurich, Switzerland
    Recruiting
07

Registry details

Key details

Study ID
NCT07546292
Lead sponsor
Silvia Brem
Collaborators
Swiss National Science Foundation
Responsible party
Silvia Brem (Head - Developmental Cognitive Neuroscience Group, Psychiatric University Hospital, Zurich) — Sponsor-investigator
First posted
Apr 22, 2026
Start date
Apr 23, 2026
Primary completion
Jun 2027 (estimated)
Completion
Jun 2027 (estimated)
Last update
May 22, 2026

Study contacts

Silvia Brem, Prof. Dr.
Contact
silvia.brem@kjpd.uzh.ch
+41 (0)58 384 67 11

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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