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Behavioural Intervention
HD-tDCS combined with CT for Memory Loss
N/A
Waitlist Available
Research Sponsored by Medical College of Wisconsin
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age ≥50-90 years
Right handed
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
Study Summary
This trial will test if a new brain stimulation technique called HD-tDCS can improve cognitive function in patients with MCI.
Eligible Conditions
- Memory Loss
- Mild Cognitive Impairment
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Treatment completion rates
Secondary outcome measures
Recruitment rate
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: HD-tDCS combined with CTActive Control1 Intervention
HD-tDCS combined with CT, administered to participants with amnestic MCI (aMCI) in blocks of 5 daily treatments for a total of 15 sessions. There will be one treatment block/month for a total of 3 months
Group II: sham HD-tDCS combined with CTPlacebo Group1 Intervention
sham HD-tDCS combined with CT, administered to participants with amnestic MCI (aMCI) in blocks of 5 daily treatments for a total of 15 sessions. There will be one treatment block/month for a total of 3 months
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Who is running the clinical trial?
Medical College of WisconsinLead Sponsor
604 Previous Clinical Trials
1,162,248 Total Patients Enrolled
Frequently Asked Questions
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