Understanding How Alzheimer's Disease Impacts the Therapeutic Response to Transcranial Direct Current Stimulation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50-90
SponsorBaycrest

About this trial

There is currently little symptomatic therapy for Alzheimer's Disease (AD) and nothing effective for individuals with Frontotemporal dementia (FTD). However, neuromodulation with transcranial direct current stimulation (tDCS) has the potential to be a clinically effective therapy for both AD and FTD. The challenge now is to specify the parameters and conditions under which tDCS is most effective to transition from the laboratory to clinical medicine. tDCS studies typically report significant group effects despite the variability demonstrated among participants, with some showing clear, meaningful improvement, while others only show statistical improvement or none at all. These variable results may be related to the conventional stimulation intensity level of 2mA. The investigators predict that administering tDCS at 4.0 mA, a more significant number of participants would show a meaningful response, and those who improve at 2mA may improve even more from 4.0mA due to having a larger electric field produced. The investigators aim to test this hypothesis in people with Alzheimer's Disease.

Eligibility criteria

Qualifiers

Mild to Moderate AD

Score between 18 and 25 on the MoCA

Able to do the N-Back task during the initial screening

Disqualifiers

No history of stroke or TBI

No shunts or metal in the body

No history of significant heart disease, alcoholism and drug use

Trial design

Treatments tested in this trial

  • tDCS and Cognitive Training

Treatment groups

42 Participants
are divided into 3 treatment groups

Sponsors and collaborators

Baycrest

Lead sponsor

BrightFocus Foundation

Collaborator