A Study of HD-tDCS and Cognitive Training to Improve Cognitive Function in MCI
Completed · Not applicable · Has a placebo group
Conditions studied: Mild Cognitive Impairment, Memory Disorders, Memory Loss
In brief
The primary objective of this project is to assess the feasibility of multi-field, extended HD-tDCS (MFE-HD-tDCS) with simultaneous computerized CT as a viable intervention to improve cognitive function in patients with MCI. This double-blinded, randomized pilot clinical trial of repetitive daily HD-tDCS/sham HD-tDCS, administered in combination with CT to subjects with MCI in 3 monthly blocks of 5 daily sessions for a total of 15 sessions will enroll 8 participants.
Key facts
- Study ID
- NCT04246164
- Run by
- Medical College of Wisconsin
- People needed
- 8
- Starts
- 2021-01-25
- Expected to finish
- 2023-02-23
- Last updated by the study team
- 2026-04-23
Who can join
Age: 50 and older, up to 90. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥50-90 years
- Willing and able to undergo all procedures
- Retains decisional capacity at initial visit
- Meets criteria for MCI, amnestic type (Petersen, 2004).
You may not qualify if…
- Significant kidney injury requiring hemodialysis
- Automatic Internal Cardiac Defibrillator (AICD) or Pacemaker
- Significant congestive heart failure
- History of clinically significant ischemic or hemorrhagic stroke, or lacune or infarct considered by radiologist likely to cause or contribute significantly to cognitive symptoms
- History of thalamic lacunar stroke
- Modified Hachinski Ischemia Score >4 points
- History of seizure disorder requiring medication
- History of brain surgery (for seizure disorder, aneurysms, or benign/malignant tumor)
- History of HIV/AIDS
- Severe untreated obstructive sleep apnea
- Greater than three servings alcohol daily or illicit drug use
- Major neurologic disorders other than dementia (e.g., MS, ALS)
- Schizophrenia, bipolar disorder, other serious mental illnesses
- Other significant medical conditions at investigators' discretion
- Pregnancy
- Lack of study partner (Participants are allowed to find a new study partner if the original study partner withdraws)
Where it is running
- The Medical College of Wisconsin — Milwaukee, Wisconsin, United States
Full record on ClinicalTrials.gov
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