Recruiting

tDCS

Sponsor:

Lady Davis Institute

Code:

NCT04524338

Conditions

Alzheimer Disease

Eligibility Criteria

Sex: All

Age: 50 - 70+

Healthy Volunteers: Not accepted

Interventions

Transcranial Direct Current Stimulation

Study Details

Brief summary:

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

Alzheimer Disease

Study ID

NCT04524338

Start date

Feb 22, 2021

Status verified date

Aug, 2024

Completion date

Oct 31, 2026

Anticipated

Primary completion date

Oct 31, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 50 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Diagnosis of Alzheimer's Disease or other form of dementia (e.g., Primary Progressive Aphasia)

Exclusion Criteria:

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

Study Design

Enrollment

20 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: At Home tDCS Users

Participants conducting tDCS at home

Interventions

Transcranial Direct Current Stimulation

Brain Stimulation Devices attached to scalp

Primary outcome measure

  • General Cognition [ Time Frame: two years ]

Central Contacts and Locations

Locations

Perform Centre

Recruiting

Montreal, Quebec, Canada, H4B 1R6

Contacts

More Information

Sponsor

Lady Davis Institute

Last update posted

Aug 13, 2024

Last verified

Aug, 2024

Keywords

  • Transcranial Direct Current Stimulation

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Lady Davis Institute on 2024-08-13.