RecruitingNot ApplicableNCT05508841

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


Sponsor

Baycrest

Enrollment

42 participants

Start Date

Sep 1, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

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

Min Age: 50 YearsMax Age: 90 Years

Plain Language Summary

Simplified for easier understanding

This study investigates how Alzheimer's disease affects the brain's response to a non-invasive brain stimulation technique called transcranial direct current stimulation (tDCS). Researchers want to understand whether the disease changes how effective this therapy is at improving memory and thinking. **You may be eligible if...** - You have been diagnosed with mild to moderate Alzheimer's disease - You scored between 18 and 25 on a cognitive test called the MoCA (Montreal Cognitive Assessment) - You are able to complete a memory task (N-Back task) during screening **You may NOT be eligible if...** - You have a history of stroke or traumatic brain injury - You have shunts or metal implants in your body or head - You have a significant history of heart disease, alcoholism, or drug use - You are taking medications that could interfere with brain stimulation effects - You are unable to cooperate with study procedures Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERtDCS and Cognitive Training

Participants will receive mild stimulation or no stimulation along with cognitive training


Locations(1)

Baycrest Health Sciences

Toronto, Ontario, Canada

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NCT05508841


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