Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06804642

Spinal Cord Stimulation for Parkinson's Disease Rehabilitation

Led by University of Louisville · Updated on 2026-03-11

20

Participants Needed

1

Research Sites

576 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study explores the use of multifunctional, non-invasive spinal cord transcutaneous stimulation (scTS) to address axial motor symptoms, particularly gait dysfunction, in Parkinson's disease (PD). These symptoms, resistant to levodopa and inadequately managed by deep brain stimulation (DBS), arise from maladaptive spinal network changes. A non-invasive approach like scTS could overcome limitations associated with invasive spinal cord stimulation (SCS), which requires surgical implantation and lacks adaptability in stimulation site adjustments. Gait dysfunction in PD stems from disrupted interactions between spinal and supraspinal networks. scTS provides a non-invasive alternative, shown to enhance locomotor functions in conditions such as spinal cord injury, stroke, and cerebral palsy. This study hypothesizes that scTS applied at multiple spinal levels-cervical (C3-C4), thoracic (T11-T12), and lumbar (L1, L2-L3)-can synergistically activate locomotor central pattern generators (CPGs) and improve gait and postural control in PD. Additionally, it is hypothesized that proprioceptive input, combined with scTS, can counteract disruptions in spinal networks and restore voluntary movement. The primary goal is to evaluate the effects of scTS on stepping performance, postural control, and locomotor recovery in PD. Specific objectives include: 1. Enhancing Locomotor Networks * Determine optimal scTS parameters for inducing rhythmic stepping in PD patients. * Assess interactions between spinal and supraspinal networks during imagined stepping under scTS in a gravity-neutral setting. 2. Improving Postural Networks o Evaluate the effectiveness of scTS in restoring postural control and integrating postural-locomotor functions. 3. Facilitating Neuroplasticity for Movement Recovery o Combine scTS with activity-based recovery training to promote adaptive plasticity in spinal and cortical networks, reducing freezing of gait (FOG). The research will measure scTS's capacity to generate coordinated stepping and postural movements, integrate proprioceptive feedback, and induce long-term improvements in gait parameters. By targeting spinal locomotor and postural systems, scTS offers a novel, non-invasive approach to addressing gaps in the management of PD gait dysfunction. This work has the potential to significantly enhance the quality of life for individuals with PD, providing a safe, adaptable, and patient-centered therapeutic solution.

CONDITIONS

Official Title

Spinal Cord Stimulation for Parkinson's Disease Rehabilitation

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of Parkinson's disease
  • Adults aged 18 to 80 years
  • Competent to give informed consent for the research protocol
  • Able to understand instructions
  • Able to ambulate 10-meters
Not Eligible

You will not qualify if you...

  • Co-morbidities affecting gait
  • Clinically significant cognitive dysfunction
  • Clinically significant depression or major active psychiatric illness such as schizophrenia, bipolar disorder, or major depressive disorder
  • Terminal illness associated with <12-month survival
  • Current diagnosis or condition such as major cardiac insufficiency, determined clinically by study doctors
  • Current uncontrolled or unmanageable alcohol or substance abuse
  • Individuals unable to communicate with the investigator and study staff
  • Any illness that study doctors believe may prevent participation in spinal cord stimulation, activity-based recovery training, or study assessments

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Frazier Rehab Institute

Louisville, Kentucky, United States, 40202

Actively Recruiting

Loading map...

Research Team

A

Andrea Wilhite, MS

CONTACT

K

Kristin Benton, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here