Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
Healthy Volunteers
NCT05947279

Examining Lateralized Aspects of Motor Control Using Non-invasive Neural Stimulation

Led by Virginia Commonwealth University · Updated on 2026-03-13

60

Participants Needed

1

Research Sites

123 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Motor adaptation and generalization are believed to occur via the integration of various forms of sensory feedback for a congruent representation of the body's position in space along with estimation of inertial properties of the limb segments for accurate specification of movement. Thus, motor adaptation is often studied within curated environments incorporating a "mis-match" between different sensory systems (i.e. a visual field shift via prism googles or a visuomotor rotation via virtual reality environment) and observing how motor plans change based on this mis-match. However, these adaptations are environment-specific and show little generalization outside of their restricted experimental setup. There remains a need for motor adaptation research that demonstrates motor learning that generalizes to other environments and movement types. This work could then inform physical and occupational therapy neurorehabilitation interventions targeted at addressing motor deficits.

CONDITIONS

Official Title

Examining Lateralized Aspects of Motor Control Using Non-invasive Neural Stimulation

Who Can Participate

Age: 18Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Right-handed as determined by the short-form Edinburgh Handedness Inventory
  • Between the ages of 18 and 40
Not Eligible

You will not qualify if you...

  • Mixed- or left-handed as determined by the short-form Edinburgh Handedness Inventory
  • Self-reported history of seizure and/or diagnosis of epilepsy
  • History of fainting spells
  • History of concussion with loss of consciousness
  • History of ringing in the ears (tinnitus)
  • Presence of cochlear implants
  • History of migraines
  • Diagnosed psychological or neurological condition
  • Metal in the scalp
  • Any previous adverse reaction to a brain stimulation technique
  • Any previous adverse reaction to 3D virtual reality environments (i.e., 'cybersickness')
  • Possibility of being currently pregnant (for females only)
  • Current open head wound or skin condition of the scalp
  • Current implanted device(s) such as cardiac pacemaker

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Virginia Commonwealth University Medical Center

Richmond, Virginia, United States, 23219

Actively Recruiting

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Research Team

B

Brooke Dexheimer, PhD, OTD, OTR/L

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

3

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