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NCT Number: NCT06473714

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

Primary progressive aphasia (PPA) is a focal dementia characterized by primary impairment of language abilities and functional disturbances associated with language.

Although PPA is a progressive disorder, new techniques are being proposed to try to activate parts of the brain previously thought to be potentially inactive, due to the possibility of "neuroplasticity". This concept refers to our brain's modularity and learning potential. Transcranial direct current stimulation is a powerful neuromodulatory technique, in which a small current is applied to the participant's scalp through the targeted positioning of an anode and a cathode. The positive or anodal stimulation of tDCS is supposed to increase neuronal activity under the electrode, while cathodal stimulation is supposed to do the opposite.

This project will provide new insights into the nature of the neural activity underlying executive functions in people with primary progressive aphasia compared to those without. The investigators expect to find reduced amplitude of electrophysiological responses and lower accuracy in people with primary progressive aphasia compared with healthy controls. Given the results of previous studies showing the efficacy of tDCS protocols in the treatment of aphasia, the investigators might expect them to improve executive functions. If so, the investigators expect significantly greater electrophysiological responses after stimulation sessions compared with sham conditions. This project is of great clinical relevance. This research will improve current therapeutic protocols used in the treatment of PPA by providing critical findings on whether and how the use of tDCS improves executive functions. Crucially, the research will advance knowledge of executive function decline as a sensitive marker of PPA, informing us about the possibility of early detection of this disorder. At the same time, the investigators will analyze the possibility of controlling symptomatological evolution via the analysis of acoustic and vocal markers. This will enable us to observe the evolution of sensory markers such as acoustic markers according to symptomatological evolution. This will enable us to check whether acoustic markers correlate with the patient's level of symptomatological impairment and/or pathological physiological data.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU de Nice

Nice, France

Location status: Recruiting

Location contact

Justine LEMAIRE

CONTACT

+33492034778

Who can participate

Healthy volunteers accepted: No

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

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

Treatment and study plan

tDCS

Device

Transcranial direct current stimulation of the dorsolateral prefrontal cortex will be made at 1,5mA

SHAM

Device

Transcranial direct current stimulation of the dorsolateral prefrontal cortex will not be made. The electrodes are placed on the skull and a slight but non-continuous intensity is applied.

Primary outcomes

  1. Flanker task

    Time frame: 6 week

  2. Stroop task

    Time frame: 6 week

Study contacts

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

Auriane Gros, Pr

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Nice

Other

Registry information

Acronym: Stim-APHA

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Jun 25, 2024
Registry last updated
Nov 5, 2024

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

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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.

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