Clinical trial Recruiting at 1 site Interventional Ages 65 to 85

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 typeInterventional
Ages65 Years to 85 Years
SexAll
Enrollment40 (estimated)
SponsorUniversity of Michigan
Academic / other
Locations1 site (Ann Arbor, Michigan)
StatusRecruiting
StartedFebruary 25, 2025
Main results expectedJanuary 25, 2027
Study endsJanuary 25, 2027
Registry record updatedOctober 20, 2026
Trial IDNCT06561165 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

  • 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.