Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07546292

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

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).

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital of Psychiatry

Zurich, Switzerland

Location status: Recruiting

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Transcranial random noise stimulation

Other

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.

Sham stimulation

Other

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.

Primary outcomes

  1. Performance in the artificial orthography learning task

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

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

  2. fMRI activation and connectivity during print processing

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

    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.

Secondary outcomes

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

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

    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.

  2. Reading and reading-related behavioral measures

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

    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.

  3. Performance in further cognitive tasks

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

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

Study contacts

Contact information is provided by the study sponsor or research team.

Silvia Brem, Prof. Dr.

CONTACT

[email protected]

+41 (0)58 384 67 11

Sponsors and collaborators

Lead sponsor

Silvia Brem

Other

Collaborators

  • Swiss National Science Foundation

Registry information

Official study title

Transcranial Electrical Stimulation and the Reading Brain: Toward Novel Interventions for Reading Impairments

Acronym: LexiStim

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Apr 22, 2026
Registry last updated
May 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.