Actively Recruiting

Age: 21Years - 75Years
All Genders
Healthy Volunteers
NCT05286736

Neuroplasticity in Parkinson's Disease

Led by University of Minnesota · Updated on 2025-08-08

50

Participants Needed

1

Research Sites

401 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this project is to increase our understanding of the early state and temporal evolution of neuroplastic changes in the cortex and subthalamic nucleus (STN) of people with PD, and the relationship of these changes to the emergence and expression of PD motor and non-motor signs. Neurophysiological biomarkers derived from this work may be important for the early detection and prediction of progression of disease. They can also provide the means to assess the efficacy of interventions designed to prevent or slow disease progression.

CONDITIONS

Official Title

Neuroplasticity in Parkinson's Disease

Who Can Participate

Age: 21Years - 75Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants with Parkinson's Disease diagnosed by a neurologist using PD Society Brain Bank criteria
  • Not receiving levodopa or dopamine agonist treatment at the start of the study
  • Able to walk independently without assistive devices for 50 meters
  • Healthy controls matched by age (+/- 3 years) and sex to PD participants
  • Healthy controls able to walk independently without assistive devices for 50 meters
Not Eligible

You will not qualify if you...

  • Diagnosed dementia or impaired capacity to consent
  • History of musculoskeletal disorders affecting limb movement
  • History of bipolar disorder, PTSD, or major depression
  • Other neurological disorders affecting study participation
  • Implanted deep brain stimulation or neurosurgery for Parkinson's
  • Pregnancy
  • History of seizures, epilepsy, stroke, multiple sclerosis, or traumatic brain injury (for TMS experiments)
  • Recent frequent fainting episodes due to blood, emotional, or sensory triggers (for TMS)
  • Intracranial metallic or magnetic implants
  • Pacemaker or implanted medical devices
  • History of surgery on blood vessels, brain, or heart
  • Unexplained recurring headaches or concussion in past six months
  • Severe hearing impairment

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

University of Minnesota

Minneapolis, Minnesota, United States, 55455

Actively Recruiting

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Research Team

C

Colum MacKinnon, PhD

CONTACT

M

Madison Aasen

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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