Clinical trial Recruiting at 1 site Interventional Ages 18 to 35

Cortical Excitability and DLPFC Structure in Healthy Adults Using TMS, EEG, and High-Field MRI

Official title: Study of the Correlation Between Cortical Excitability and Cytoarchitectonics of Prefrontal Cortex in Healthy Adult Participants, Using Transcranial Magnetic Stimulation Coupled to EEG and High-field MRI

Run by Institut National de la Santé Et de la Recherche Médicale, France · NCT07071259 · Data updated 2026-11-12

This study tests how reproducible brain signals from transcranial magnetic stimulation relate to the anatomy of the left prefrontal cortex in healthy adults.

Quick facts

Study typeInterventional
Ages18 Years to 35 Years
SexAll
Enrollment34 (estimated)
SponsorInstitut National de la Santé Et de la Recherche Médicale, France
Government
Locations1 site (Marseille)
StatusRecruiting
StartedJune 29, 2026
Main results expectedApril 2028
Study endsApril 2028
Registry record updatedJuly 7, 2026
Trial IDNCT07071259 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Healthy adults aged 18 to 35 who are right-handed and meet all inclusion criteria.

Probably not a fit

Individuals with current medical or psychiatric conditions or those not qualified as healthy volunteers are unlikely to benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Healthy adults will receive repetitive transcranial magnetic stimulation (rTMS) targeting the dorsolateral prefrontal cortex while EEG and high-field MRI measurements are recorded to explore links between cortical excitability and prefrontal cytoarchitectonics. The study builds on prior small-sample findings suggesting EEG and brain structure patterns may correspond to response tendencies. It uses TMS stimulation with concurrent neuroimaging while monitoring safety and comfort. No disease treatment is being tested in this nonpatient population. The aim is to better understand brain–structure–function relationships in the DLPFC under TMS.

Why it matters

Potential benefit: If successful, findings could improve understanding of how brain structure relates to stimulation effects, informing future personalized brain stimulation approaches.

How similar studies have gone: Previous small studies have shown patterns in EEG theta activity linked to TMS response, but results have varied and standardization is ongoing.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* People aged 18 to 35
* People affiliated with a social security scheme or beneficiary of such a scheme
* People who have signed the informed consent
* Right-handed people
* People with a body mass index between 18 and 26
* People able to abstain from alcohol for 24 hours prior to the experiment
* People able to remain perfectly still for 15 minutes straight, and able to have reduced mobility for 3 hours
* People able to of not using narcotics (marijuana, cocaine, ecstasy, MDMA, ketamine, etc.) during the 15 days preceeding the experiment.
* Conducting a pregnancy test before inclusion for women of childbearing age and when the research is conducted over a long period, at a frequency adapted to the gaze of the research acts
* Effective contraception for women of childbearing potential

Exclusion Criteria:

* Pregnant, parturient, or breastfeeding
* Protected adults
* Minors
* People staying in a healthcare or social institution
* People in an emergency situation
* People deprived of their liberty
* People with the usual contraindications to MRI

  * Ferromagnetic surgical clips, ocular implants, metallic foreign bodies intraocularly or in the nervous system, implants or metallic objects susceptible to concentrate the radio frequency field, cochlear implants, brain stimulator or cardiac pacemaker, presence of a craniotomy scar, agitation
  * Claustrophobia
  * Large, black tattoo close to the orofacial area
* People not wishing to be informed of abnormalities discovered at the MRI
* People with a history of epilepsy or suffering from epilepsy
* Individuals whose parents, children, siblings, or parents have a history of epilepsy
* People with known neurological and/or psychiatric disorders with past and/or current medical treatment, or drug addiction
* Staff with a hierarchical link to the investigators

Where it's running

  • Hôpital la Timone
    Marseille, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.