NCT07554105

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
20mo left

Started Mar 2026

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress8%
Mar 2026Dec 2027

Study Start

First participant enrolled

March 17, 2026

Completed
24 days until next milestone

First Submitted

Initial submission to the registry

April 10, 2026

Completed
18 days until next milestone

First Posted

Study publicly available on registry

April 28, 2026

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2027

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2027

Last Updated

April 28, 2026

Status Verified

April 1, 2026

Enrollment Period

1.5 years

First QC Date

April 10, 2026

Last Update Submit

April 20, 2026

Conditions

Keywords

languagetRNS

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

OTHER

age 15-35 years

Device: transcranial random noise stimulationDevice: sham stimulation

Elderly adults

OTHER

age 60-90 years

Device: transcranial random noise stimulationDevice: sham stimulation

Interventions

active HD-tRNS

Elderly adultsYounger adults

current will be ramped up for 30 seconds and then switched of, to mimic the subjective sensation of tRNS.

Elderly adultsYounger adults

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

MeSH Terms

Conditions

Language

Interventions

Transcranial Direct Current Stimulation

Condition Hierarchy (Ancestors)

CommunicationBehavior

Intervention Hierarchy (Ancestors)

Electric Stimulation TherapyTherapeuticsConvulsive TherapyPsychiatric Somatic TherapiesBehavioral Disciplines and ActivitiesElectroshockPsychological Techniques

Central Study Contacts

Adrian Guggisberg, MD

CONTACT

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

EEG and behavioral data

Time Frame
After publication
Access Criteria
Depository

Locations