Actively Recruiting

Phase Not Applicable
Age: 50Years - 90Years
All Genders
NCT05508841

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

Led by Baycrest · Updated on 2024-08-13

42

Participants Needed

1

Research Sites

226 weeks

Total Duration

On this page

Sponsors

B

Baycrest

Lead Sponsor

B

BrightFocus Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 50Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Mild to Moderate AD
  • Score between 18 and 25 on the MoCA
  • Able to do the N-Back task during the initial screening
Not Eligible

You will not qualify if you...

  • History of stroke or traumatic brain injury
  • Presence of shunts or metal in the body
  • History of significant heart disease, alcoholism, or drug use

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Baycrest Health Sciences

Toronto, Ontario, Canada, M6A 2E1

Actively Recruiting

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Research Team

C

Carlos Roncero, PhD

CONTACT

Y

Yashna Kochar, H BSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

3

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