Actively Recruiting

Phase Not Applicable
Age: 50Years - 100Years
All Genders
NCT04524338

Longitudinal Study Examining At-Home tDCS

Led by Lady Davis Institute · Updated on 2024-08-13

20

Participants Needed

1

Research Sites

296 weeks

Total Duration

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AI-Summary

What this Trial Is About

Participants with dementia have reported improvements after receiving tDCS in a study at our lab. Although we make an effort to enroll such participants in further tDCS research studies, some participants are ineligible for further studies or simply unwilling to continue being a research participant. These same individuals, however, are interested in purchasing their own tDCS machine and have approached us for advice on how to purchase their own machine. Because these devices are commercially available, there is nothing theoretically stopping these participants from purchasing their own machine. Therefore, we have chosen to carry out a longitudinal study that will allow us to serve as an advisory role for participants who have decided to continue administering tDCS at home. We will recommend the tDCS related items that should be purchased, and train participants on how to properly administer tDCS. Monthly reports will also be collected, which will allow us to monitor the person's condition. We plan to monitor participants for at least two years. From these reports, we will be able determine to what extent tDCS is beneficial when done at home as a treatment for dementia symptoms.

CONDITIONS

Official Title

Longitudinal Study Examining At-Home tDCS

Who Can Participate

Age: 50Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of Alzheimer's Disease or other form of dementia (e.g., Primary Progressive Aphasia)
Not Eligible

You will not qualify if you...

  • Metal in the head or other factors that would make stimulation unsafe

AI-Screening

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Trial Site Locations

Total: 1 location

1

Perform Centre

Montreal, Quebec, Canada, H4B 1R6

Actively Recruiting

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Research Team

S

Shelley Solomon

CONTACT

J

Jacinta Lesmond

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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