The purpose of this study is to assess acceptability, and safety of providing tDCS to ADRD patients with behavioral symptoms and to assess the efficacy of tDCS for ADRD-related symptoms, mainly behavioral symptoms.
Age range
60 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Acceptability of the tDCS Treatment as Assessed by the tDCS Acceptability Questionnaire
Timeframe: week 2
Acceptability of the tDCS Treatment as Assessed by the tDCS Acceptability Questionnaire
Timeframe: week 4
Acceptability of the tDCS Treatment as Assessed by the tDCS Acceptability Questionnaire
Timeframe: week 6
Acceptability of the tDCS Treatment as Assessed by the tDCS Acceptability Questionnaire
Timeframe: week 12
Safety as Assessed by the Side Effects Questionnaire
Timeframe: week 2
Safety as Assessed by the Side Effects Questionnaire
Timeframe: week 4
Safety as Assessed by the Side Effects Questionnaire
Timeframe: week 6