Effect of Transcranial Random Noise Stimulation on the Performance in Language Tasks
tRNSlang
1 other identifier
interventional
90
1 country
1
Brief Summary
Language is an essential part of daily life, enabling us to communicate, understand others, read, and learn. Certain brain injuries can disrupt these abilities, and current treatments do not always lead to a full recovery. To improve future therapeutic approaches, it is necessary to better understand how the brain processes language and how its activity can be modulated. This study aims to evaluate the effects of a non-invasive brain stimulation technique called transcranial random noise stimulation. This method involves applying a very weak electrical current to the scalp to modulate the activity of brain regions involved in language. It is commonly used in research and is considered safe when administered in accordance with current guidelines. Healthy adult volunteers will participate in this study. Each participant will take part in two sessions spaced about a week apart. During one session, active stimulation will be used, and during the other, placebo stimulation will be used. Placebo stimulation resembles the actual stimulation but has no active effect. Neither the participants nor the researchers will know which type of stimulation is being used during each session. During the sessions, participants will perform various language tasks, and their brain activity will be recorded using an electroencephalogram (EEG), a painless method. This study does not provide any direct benefit to participants. The risks are low and limited to temporary sensations, such as a tingling sensation on the scalp. The results will provide a better understanding of how the brain processes language and could eventually contribute to the development of new rehabilitation approaches.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2026
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 17, 2026
CompletedFirst Submitted
Initial submission to the registry
April 10, 2026
CompletedFirst Posted
Study publicly available on registry
April 28, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2027
April 28, 2026
April 1, 2026
1.5 years
April 10, 2026
April 20, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Composite score
composite behavioural score reflecting overall language performance across four language domains (phonological, semantic, morphosyntactic, and reading)
Periprocedural
Secondary Outcomes (5)
Phonological processing
Periprocedural
Semantic processing
Periprocedural
Morphosyntactic processing
Periprocedural
Reading speed
Periprocedural
Sustained attention
Periprocedural
Study Arms (2)
Younger adults
OTHERage 15-35 years
Elderly adults
OTHERage 60-90 years
Interventions
current will be ramped up for 30 seconds and then switched of, to mimic the subjective sensation of tRNS.
Eligibility Criteria
You may qualify if:
- Age: 18-35 years or 60-90 years
- Native French speakers
- Right handed
- Willing and able to provide informed consent
- Normal or corrected-to-normal vision and hearing
You may not qualify if:
- History of neurological or psychiatric disease
- Regular consumption of benzodiazepines, neuroleptics, or psychoactive drugs
- Major language deficit, developmental language disorder, arthropathies and other mechanical language impairments
- Inability to understand or follow study procedures
- Contraindications to brain stimulation, such as
- History of epilepsy or severe migraine
- Pacemaker or other active implants
- Metallic objects in the head
- Skull breach such as craniotomy
- Pregnancy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Division of Neurorehabilitation, University Hospital of Geneva
Geneva, Canton of Geneva, 1211, Switzerland
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Head of Neurorehabilitation
Study Record Dates
First Submitted
April 10, 2026
First Posted
April 28, 2026
Study Start
March 17, 2026
Primary Completion (Estimated)
September 30, 2027
Study Completion (Estimated)
December 31, 2027
Last Updated
April 28, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will share
- Time Frame
- After publication
- Access Criteria
- Depository
EEG and behavioral data