Using brain stimulation to improve hand movement control
Official title: Personalizing Multifocal Transcranial Direct Stimulation Dose to Target the Motor Network in Older Adults
Run by University of Michigan · NCT06561165 · Data updated 2026-11-12
This study is testing whether a personalized brain stimulation technique can help healthy people improve their hand movement control better than a standard method.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 65 Years to 85 Years |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | University of Michigan Academic / other |
| Locations | 1 site (Ann Arbor, Michigan) |
| Status | Recruiting |
| Started | February 25, 2025 |
| Main results expected | January 25, 2027 |
| Study ends | January 25, 2027 |
| Registry record updated | October 20, 2026 |
| Trial ID | NCT06561165 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are healthy, right-handed individuals with normal or corrected-to-normal vision who can provide written consent.
✕Probably not a fit
Patients who are left-handed, pregnant, or have a history of neurological disorders will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates how non-invasive brain stimulation, specifically high-density transcranial direct current stimulation (HD-tDCS), can enhance motor function in healthy individuals. Participants will be randomly assigned to receive either a standard HD-tDCS intervention or a personalized, dose-controlled multifocal network-targeted HD-tDCS. The goal is to determine if personalized stimulation can lead to greater improvements in manual dexterity compared to standard methods. Functional Magnetic Resonance Imaging (fMRI) will be utilized to assess brain activity during the interventions.
Why it matters
Potential benefit: If successful, this approach could lead to improved rehabilitation techniques for enhancing motor function in various populations.
How similar studies have gone: Previous studies using non-invasive brain stimulation techniques have shown promise in improving motor function, suggesting potential success for this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participants should be in good health with normal or corrected-to-normal visual acuity * Right handed * No history of neurological disorder * English speaker * Able to provide written consent prior to admission Exclusion Criteria: * Left-handed * Participants are pregnant, suspect pregnancy or are attempting to become pregnant * Have a pacemaker, intracardiac lines or any other medically implanted device or medicine pump * Have cochlear hearing implants * Taking drugs known to influence neural receptors that facilitate neuroplasticity (see protocol) * Have non removable body piercings or have foreign objects in body * Have metal anywhere in the head that could increase risk of serious injury (not including braces, dental fillings, etc.) (see protocol) * Have a personal or family history of seizure/epilepsy * Taking prescription drugs that lower the threshold for seizures * Recent history of excessive alcohol consumption * History of alcohol addiction/dependence * Recent history of recreational drug use * History of drug addiction/dependence * Recent history of recreational drug use * History of drug addiction/dependence * Diagnosed with a stroke, brain hemorrhage, brain tumor, encephalitis. * Diagnosed with multiple sclerosis * Diagnosed with Parkinson's disease or Alzheimer's disease * Diagnosed with depression in the past 6 months * Diagnosed with attention deficit disorder, schizophrenia, manic depressive (bipolar) disorder * Diagnosed with normal pressure hydrocephalus or increased intra-cranial pressure * Diabetes requiring insulin treatment * Any serious heart disorder or liver disease
Where it's running
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University of Michigan
Ann Arbor, Michigan, United States Recruiting
Study contacts
- Principal investigator: Michael Vesia, PhD — University of Michigan
- Study coordinator: Michael Vesia, PhD
- Email: mvesia@umich.edu
- Phone: 734-764-5237
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.