Actively Recruiting

Phase Not Applicable
Age: 50Years - 80Years
All Genders
Healthy Volunteers
ID03887481

Targeting Language-specific and Executive-control Networks With Transcranial Direct Current Stimulation in Aphasic Alzheimer's Disease (Logopenic Variant PPA)

Led by Johns Hopkins University · Updated on 2025-09-15

60

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

J

Johns Hopkins University

Lead Sponsor

N

National Institute on Aging (NIA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating transcranial direct current stimulation (tDCS) combined with language therapy to improve language and cognitive functions in people with logopenic variant Primary Progressive Aphasia (lvPPA), a form of Alzheimer's disease that severely affects language and communication. This condition typically begins between the ages of 50 and 65, impacting work and family life. The study builds on previous findings that tDCS over a brain language center enhances therapy effects and explores stimulation of two brain areas to test how benefits may generalize to different language and executive functions. Participants will undergo two treatment periods separated by a three-month break. They will receive either active high-definition tDCS (HD-tDCS) combined with language and cognitive interventions or a sham (inactive) stimulation combined with the same interventions. The stimulation targets either the left supramarginal gyrus (involved in phonological memory) or the left dorsolateral prefrontal cortex (involved in executive control). Each stimulation session lasts up to 20 minutes with 2 milliamperes of current. During the study, participants will be assessed before, immediately after, and up to three months following each intervention. Assessments include language tests measuring word and sentence repetition, memory spans, naming, spelling, and connected speech, along with brain imaging scans to monitor functional connectivity and neurotransmitter levels. The study also collects data on cognitive, clinical, physiological, and demographic factors to identify predictors of treatment response. Total participation includes both treatment phases and follow-up evaluations.

CONDITIONS

Brief Title

Targeting Language-specific and Executive-control Networks With Transcranial Direct Current Stimulation in Logopenic Variant PPA

Who Can Participate

Age: 50Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Must be between 50-80 years of age.
  • Must be right-handed.
  • Must be proficient in English.
  • Must have a minimum of high-school education.
  • Must be diagnosed with Primary Progressive Aphasia (PPA) or dementia.
  • Diagnosis based on current consensus criteria in specialized or early dementias clinics.
  • Healthy age- and education-matched controls may be included.
Not Eligible

You will not qualify if you...

  • Previous neurological diseases including vascular dementia, stroke, developmental dyslexia, dysgraphia, or attentional deficit.
  • Uncorrected hearing loss.
  • Uncorrected visual acuity loss.
  • Advanced dementia or severe language impairments (MMSE <18, MOCA <15, or FTD-CDR ≤2).
  • Left-handed individuals.
  • Pre-existing psychiatric disorders such as severe depression or schizophrenia that prevent study compliance.
  • Severe claustrophobia.
  • Presence of cardiac pacemakers or ferromagnetic implants.
  • Pregnant women.

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Approximately 6 weeks per treatment phase with a 3-month washout period between treatments

Participants receive either active high-definition transcranial direct current stimulation (HD-tDCS) combined with language and cognitive exercises, or sham stimulation combined with language and cognitive exercises, in a crossover design with a washout period.

Multiple visits including baseline, immediately after intervention, 1 month post intervention, and 3 months post intervention assessments per treatment phase

Follow-up

Duration - 3 months post each treatment phase

Participants are monitored for changes in language, memory, and brain function up to 3 months after each treatment phase.

Visits at 1 month and 3 months post intervention per treatment phase

Trial Site Locations

Total: 1 location

1

Johns Hopkins Hospital

Baltimore, Maryland, United States, 21287

Actively Recruiting

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Research Team

C

Cesia Diaz

K

Kelly Eun

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Augmentation of spelling therapy with transcranial direct current stimulation in primary progressive aphasia: Preliminary results and challenges.

Kyrana Tsapkini, Constantine Frangakis, Yessenia Gomez...

https://pubmed.ncbi.nlm.nih.gov/26097278

Electrical brain stimulation in different variants of primary progressive aphasia: A randomized clinical trial.

Kyrana Tsapkini, Kimberly T Webster, Bronte N Ficek...

https://pubmed.ncbi.nlm.nih.gov/30258975

The use of spelling for variant classification in primary progressive aphasia: Theoretical and practical implications.

Kyriaki Neophytou, Robert W Wiley, Brenda Rapp...

https://pubmed.ncbi.nlm.nih.gov/31401078

Dissociation within the frontoparietal network in verbal working memory: a parametric functional magnetic resonance imaging study.

Anne Sophie Champod, Michael Petrides

https://pubmed.ncbi.nlm.nih.gov/20220020

The Role of Language Severity and Education in Explaining Performance on Object and Action Naming in Primary Progressive Aphasia.

Marianna Riello, Andreia V Faria, Bronte Ficek...

https://pubmed.ncbi.nlm.nih.gov/30425638