Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Using brain stimulation to improve language function in primary progressive aphasia

Official title: Effects of Transcranial Direct Current Stimulation (tDCS) on Inhibition and Brain Function in Primary Progressive Aphasia

Run by Centre Hospitalier Universitaire de Nice · NCT06473714 · Data updated 2026-11-12

This study is testing whether a type of brain stimulation can help improve language skills in people with primary progressive aphasia.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment20 (estimated)
SponsorCentre Hospitalier Universitaire de Nice
Academic / other
Locations1 site (Nice)
StatusRecruiting
StartedNovember 4, 2024
Main results expectedSeptember 2027
Study endsSeptember 2027
Registry record updatedNovember 5, 2024
Trial IDNCT06473714 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are right-handed adults over 18 years old with a diagnosis of primary progressive aphasia who can read and speak French.

Probably not a fit

Patients with severe cognitive or language disorders, neurodevelopmental or non-degenerative neurological disorders, or those with contraindications to tDCS may not benefit from this study.

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

What this trial studies

This study investigates the effects of transcranial direct current stimulation (tDCS) on brain function and inhibition in individuals diagnosed with primary progressive aphasia (PPA). By applying a small electrical current to the scalp, the study aims to enhance neuronal activity in targeted brain regions associated with language processing. Participants will undergo treatment sessions to assess changes in their language abilities and executive functions compared to a control group. The research seeks to explore the potential for neuroplasticity in the brains of individuals with PPA.

Why it matters

Potential benefit: If successful, this approach could lead to improved language function and quality of life for patients with primary progressive aphasia.

How similar studies have gone: While the use of tDCS in language disorders is an emerging field, there have been promising results in similar studies exploring its effects on cognitive functions.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Be a male or female over the age of 18 with a primary progressive aphasia diagnosis
* Available for treatment and testing sessions
* able to read and speak French
* Be right-handed

Exclusion Criteria:

* Presence of neurodevelopmental disorders or non-degenerative neurological disorders
* Post-stroke aphasia
* Language or cognitive disorders too severe to allow task performance or communication
* Pre-existing psychiatric disorders; severe depression, schizophrenia
* People with pacemakers or metal implants, epilepsy
* Presence of a medical condition that represents a contraindication to tDCS
* Active use of psychotropic drugs
* Treatment with tDCS or TMS in the last 3 months
* Additional language therapy
* Pregnancy or breast-feeding

Where it's running

  • CHU de Nice
    Nice, France
    Recruiting

Study contacts

  • Principal investigator: Auriane Gros, Pr — Centre Hospitalier Universitaire de Nice
  • Study coordinator: Auriane Gros, Pr
  • Email: gros.a2@chu-nice.fr

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.