Home-based tDCS in Frontotemporal Dementia or Alzheimer's Disease
Launched by JOHNS HOPKINS UNIVERSITY · Jul 28, 2023
Trial Information
Current as of October 15, 2025
Enrolling by invitation
Keywords
ClinConnect Summary
This study is testing whether at-home brain stimulation with a gentle electrical current (tDCS) to the left side of the brain, combined with computer-based thinking and language training, can improve thinking and language abilities in people with Primary Progressive Aphasia (PPA), Frontotemporal Dementia, Mild Cognitive Impairment (MCI), or mild Alzheimer's disease. In a cross-over design, each participant will try both approaches: (1) active tDCS plus cognitive training, and (2) active tDCS alone. The order is chosen randomly, and there is a three-month washout period between the two treatment phases. The researchers will measure changes in language skills, executive function (planning, problem-solving, attention), and overall cognitive ability.
Who may be eligible: adults roughly 50 to 90 years old with a diagnosis of PPA, Frontotemporal Dementia, MCI, or mild Alzheimer’s disease; must be right-handed, fluent in English, and have at least a high school education. Participants will be screened with language testing, brain imaging (MRI), and clinical assessment. Exclusions include significant vision or hearing problems, other major brain disorders, certain pregnancy or MRI safety issues, or devices like pacemakers. Each treatment period includes about 50 sessions over roughly 10 weeks, all conducted at home with remote support. The study is run by Johns Hopkins University in Baltimore and is currently enrolling by invitation, with a projected overall completion in late 2025.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Must be clinically diagnosed with PPA, fronto-temporal dementia (FTD), MCI or mild Alzheimer's disease (AD). Diagnosis will be based on neuropsychological testing, language testing (most commonly the Western Aphasia Battery), MRI, and clinical assessment.
- • Must be right-handed.
- • Must be proficient in English.
- • Must have a minimum high-school education.
- Exclusion Criteria:
- • Uncorrected visual or hearing impairment by self-report.
- • Stroke/other premorbid neurological disorder affecting the brain.
- • Any other developmental language-based learning disorder other than PPA.
- • Inability to follow directions for baseline tasks.
- • Pre-existing psychiatric disorders such as behavioral disturbances, severe depression, and schizophrenia that do not allow them to comply or follow the study schedule and requirements such as repeated evaluation and therapy will be excluded.
- Exclusion Criteria for MRI participation:
- • Severe claustrophobia.
- • Cardiac pacemakers or ferromagnetic implants.
- • Pregnant women.
About Johns Hopkins University
Johns Hopkins University, a prestigious research institution located in Baltimore, Maryland, is renowned for its commitment to advancing medical science and public health through innovative clinical trials. With a rich history of groundbreaking research and a multidisciplinary approach, the university's clinical trial initiatives focus on translating scientific discoveries into effective treatments and interventions. Leveraging state-of-the-art facilities and a collaborative network of experts, Johns Hopkins University conducts rigorous clinical studies that aim to improve patient outcomes and address critical health challenges. Its dedication to ethical standards and participant safety underscores its role as a leader in clinical research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Baltimore, Maryland, United States
Patients applied
Trial Officials
Kyrana Tsapkini, PhD
Principal Investigator
Johns Hopkins University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported