Longitudinal Study Examining At-Home tDCS

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50-100
SponsorLady Davis Institute

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial design

Design model

Single group

Treatments tested in this trial

  • Transcranial Direct Current Stimulation

    Device

    Brain Stimulation Devices attached to scalp

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: At Home tDCS UsersExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

General Cognition

Improved General Cognition as defined by scores on the Montreal Cognitive Assessment. Test has scores from 0-30, where higher scores reflect better cognition. In this study, an increased score would reflect an improvement in general cognition, which we would interpret as associated with the application of transcranial direct current stimulation

Time frame
two years

Secondary outcomes

Other outcomes

Sponsors and contacts

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