Actively Recruiting

Phase Not Applicable
Age: 11Years - 45Years
All Genders
Healthy Volunteers
NCT06586437

Neuromodulation of the Cortex and Spinal Cord

Led by Father Flanagan's Boys' Home · Updated on 2025-09-29

50

Participants Needed

1

Research Sites

289 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Specific Aim 1: To further quantify the difference in the sensorimotor cortical activity, spinal cord activity, and corticospinal coherence of persons with CP. Overall hypotheses: The sensorimotor cortical activity, spinal cord activity, and corticospinal coherence will be uncharacteristic in persons with CP when compared with neurotypical controls. Furthermore, the extent of the alterations in the sensorimotor cortical activity, spinal cord activity, and corticospinal coherence will be tightly linked with the clinical presentations of persons with CP. Specific Aim 2: To investigate the effect of transcutaneous current stimulation applied over the cortex and/or spinal cord on the sensorimotor cortical activity, spinal cord dynamics, and corticospinal coherence. Overall hypotheses: Compared with the sham controls, those receiving the transcutaneous current stimulation will demonstrate alterations in the strength of the sensorimotor cortical activity, spinal cord activity, and corticospinal coherence. Moreover, the extent of the alterations in the sensorimotor cortical activity, spinal cord activity, and corticospinal coherence will be tightly linked with the clinical presentations of persons with CP.

CONDITIONS

Official Title

Neuromodulation of the Cortex and Spinal Cord

Who Can Participate

Age: 11Years - 45Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Cerebral palsy participants with Gross Motor Function Classification (GMFCS) levels between I and IV
  • Neurotypical controls with no known atypical neurodevelopment such as autism, Down Syndrome, or ADHD
  • Age between 11 and 45 years
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Any condition considered by the investigator to contraindicate participation
  • Presence of any ferrous metal implant or orthodonture interfering with MEG or MRI safety
  • Orthopedic surgery within the last 6 months
  • Metal in the body that precludes MRI use

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

Boys Town National Research Hospital

Boys Town, Nebraska, United States, 68010

Actively Recruiting

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Research Team

M

Max J Kurz, PhD

CONTACT

J

Jennifer M Kime, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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