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Zapping the brain while training memory: a new hope for MCI?
NCT ID NCT04246164
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study tested whether combining a gentle brain stimulation technique called HD-tDCS with computer-based cognitive training is feasible for people with mild cognitive impairment (MCI). Eight participants completed 15 sessions over three months. The main goal was to see if people would stick with the treatment, not to prove it works. Early results suggest the approach is worth studying further in larger trials.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- high definition transcranial direct current stimulation (HD-tDCS) combined with cognitive training
- What this could lead to
- If this approach proves feasible and effective in larger trials, it could point toward a non-drug way to slow memory decline in people with mild cognitive impairment.
- What could go wrong
- This is a very small pilot study with only 8 participants, so results may not apply to everyone. The main goal was feasibility, not proof of benefit, and larger studies are needed.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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8 people
The number who actually took part.
- Started
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Jan 2021
- Finished
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Feb 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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50 to 90 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥50-90 years 2. Willing and able to undergo all procedures 3. Retains decisional capacity at initial visit 4. Meets criteria for MCI, amnestic type (Petersen, 2004). Exclusion Criteria: 1. Significant kidney injury requiring hemodialysis 2. Automatic Internal Cardiac Defibrillator (AICD) or Pacemaker 3. Significant congestive heart failure 4. History of clinically significant ischemic or hemorrhagic stroke, or lacune or infarct considered by radiologist likely to cause or contribute significantly to cognitive symptoms 5. History of thalamic lacunar stroke 6. Modified Hachinski Ischemia Score \>4 points 7. History of seizure disorder requiring medication 8. History of brain surgery (for seizure disorder, aneurysms, or benign/malignant tumor) 9. History of HIV/AIDS 10. Severe untreated obstructive sleep apnea 11. Greater than three servings alcohol daily or illicit drug use 12. Major neurologic disorders other than dementia (e.g., MS, ALS) 13. Schizophrenia, bipolar disorder, other serious mental illnesses 14. Other significant medical conditions at investigators' discretion 15. Pregnancy 16. Lack of study partner (Participants are allowed to find a new study partner if the original study partner withdraws)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
The Medical College of Wisconsin
Milwaukee, Wisconsin, 53226, United States
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