Can zapping the brain slow language decline? new trial investigates
NCT ID NCT07158216
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether two types of non-invasive brain stimulation—TMS and tDCS—can slow language decline in people with primary progressive aphasia, a condition that gradually impairs speech and understanding. Over 6 months, 80 participants will receive either real or sham stimulation along with language therapy. The goal is to see if these brain-zapping techniques can help preserve communication skills longer.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Transcranial magnetic stimulation (TMS) and transcranial direct current stimulation (tDCS)
- What this could lead to
- If successful, this could point toward a non-drug way to help people with primary progressive aphasia maintain language skills longer.
- What could go wrong
- This is an early-stage trial with only 80 participants, so results may not apply to everyone. The benefits might be small or temporary, and the stimulation can cause mild discomfort or headache.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosis of PPA according to the current consensus criteria proposed by Gorno-Tempini et al., 2011), based on the presence of progressive language impairment as the most prominent and primary cause of functional decline and the exclusion of other medical, psychiatric, or non-neurodegenerative causes,a s well as early prominent memory, visuoperceptual or behavioral disturbances; * Diagnosis of one of the three variants of PPA (non-fluent, semantic, or logopenic) according to the consensus criteria (Gorno-Tempini et al., 2011), based on the language profile and supported by neuroimaging (FDG-PET or MRI). * Clinical Dementia Rating scale equal or less than 1; * The language impairment is the main neurological deficit for the patient. Exclusion Criteria: * Patient diagnosed with a condition other than PPA that could cause language impairment; * History of epilepsy or presence of focal epileptiform pathology on EEG recording; ·Contraindications related to the treatments or procedures to be used (TMS and tDCS), such as ferromagnetic material, pregnancy, or breastfeeding; * Terminal illness or active malignancy; * Alcohol or substance abuse within the past year; * Major psychiatric disorders (schizophrenia, schizoaffective disorders, bipolar disorder, obsessive-compulsive disorder, or personality disorders); * Absolute inability to communicate (mutism), or poor command of the language that, in the investigator's judgment, would prevent participation in the study; * Severity of PPA that prevents participation in interventions or assessments at the time of inclusion; * Participation in another clinical trial within the previous 4 months; * Chronic use of medications that could affect study outcomes; * Antiepileptic drugs: allowed if on stable doses for at least 3 months before inclusion. If needed during the study due to seizure occurrence, they may be added; * Diazepam and derivatives: permitted only if on stable doses for at least 3 months before inclusion. Dose adjustments during the study are allowed; * Donepezil, Galantamine, Rivastigmine, and Memantine: allowed if on stable doses for at least 3 months before inclusion; * SSRIs (Selective Serotonin Reuptake Inhibitors): permitted only if on stable doses for at least 3 months prior to inclusion. If necessary during the study, they may be added; * Medications that may lower the seizure threshold (e.g., tricyclic antidepressants, antipsychotics): allowed if on stable doses for at least 3 months before inclusion.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hospital Clinico San Carlos
RECRUITINGMadrid, Spain
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