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Search / Trial NCT05589402

Temporary Inactivation of Strong Muscle Sensation to Improve Rehabilitation Interventions in SCI

Launched by UNIVERSITY OF TEXAS RIO GRANDE VALLEY · Oct 17, 2022

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Rehabilitation Numbing Temporary Deafferentation Induced Cortical Plasticity

ClinConnect Summary

This clinical trial is exploring a new way to help people with spinal cord injuries (SCI) recover and regain strength in their muscles. Researchers are testing whether using an over-the-counter numbing cream on the non-paralyzed muscles of the arms while exercising the paralyzed muscles can improve strength, function, and sensation. This study is open to individuals aged 18 to 75 who have had a cervical incomplete spinal cord injury for at least 18 months. Participants will need to show that they can perform certain movements and meet specific strength requirements.

If you decide to join the trial, you’ll be asked to follow some study procedures and participate in exercises. It's important to know that there are certain health conditions that might prevent someone from participating, such as having a pacemaker, a history of seizures, or current substance abuse. Overall, this study aims to find innovative ways to support rehabilitation for individuals with spinal cord injuries, potentially leading to better recovery outcomes.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • SCI Patients:
  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Male or female, aged between 18 and 75 years old
  • Have physician diagnosed cervical incomplete spinal cord injury or lesion (iSCI)
  • Classified by the American Spinal Cord Association (AIS) impairment scale as AIS C or D
  • iSCI occurred at least 18 months ago
  • Level of injury or lesion is between C2 and T1
  • Bicep strength must be classified as ≥ 3 muscle grade as defined by the medical research council scale
  • Tricep strength must be at least an MRC grade of 2 and bet at least 1 muscle grade lower than the bicep
  • Both the biceps and triceps will be required to elicit an active motor evoked potential \>200 uV with transcranial magnetic stimulation
  • Must maintain current medication regime
  • Must present with a weaker side of the body, as indicated by a Upper extremity motor score difference between the left and right side
  • UEMS \< 40 (50 max score)
  • Must be able to perform reaching movement training task
  • Healthy Controls:
  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Male or female, aged between 18 and 75 years old
  • Must be right-handed
  • Must be able to perform hand exercises
  • Exclusion Criteria:
  • SCI Patients:
  • Pacemaker or another implanted device
  • Metal in the skull
  • History of seizures
  • Pregnancy
  • First-degree relative with medication-resistant epilepsy
  • Current participation in upper limb rehabilitation therapies
  • Current use of illicit drugs, abusing alcohol, or have withdrawn from alcohol in the last 6 months
  • Other neurological impairment or condition
  • Pressure ulcers
  • Significant lower motor neuron loss at C7 as noted by a nerve conduction velocity \<50 m/s
  • History of traumatic brain injury as documented by Rancho Scale Impairment of \<5
  • History of brain MRI documented focal cerebral cortex infarct (e.g. hydrocephalus)
  • Contractures at the elbow
  • Severe spasticity as noted by a modified ashworth scale (MAS) \> 4
  • Documented, non-sedated post-traumatic amnesia lasting more than 48 hours
  • Pregnancy
  • Allergic to lidocaine
  • A neuroactive medication that has the potential to lower the seizure threshold
  • Based on documented publications in stroke, this will include bupropion (wellbutrin), psychostimulants and neuroleptics
  • All medications will be reviewed with physician, Dr. Amol Utturkar (DHR)
  • Healthy Controls:
  • Pacemaker or other implanted device
  • Metal in the skull
  • History of seizures
  • First-degree relative with medication-resistant epilepsy
  • Current use of illicit drugs (including heroin, crack/cocaine, marijuana), abusing alcohol or having withdrawn from alcohol in the last 6 months
  • Allergy to lidocaine
  • Other neurological impairment or condition
  • Pregnancy
  • A neuroactive medication that has the potential to lower the seizure threshold
  • Based on documented publications on stroke, this will include bupropion (wellbutrin), psychostimulants and neuroleptics

About University Of Texas Rio Grande Valley

The University of Texas Rio Grande Valley (UTRGV) is a prominent academic institution dedicated to advancing healthcare through innovative research and clinical trials. With a focus on addressing the unique health challenges of the Rio Grande Valley region, UTRGV integrates education, community engagement, and cutting-edge research to foster improved health outcomes. The university's commitment to diversity and inclusion enhances its ability to conduct impactful clinical trials, ensuring that research findings are relevant and beneficial to the populations it serves. Through collaborative efforts with local and national partners, UTRGV strives to contribute significantly to medical knowledge and public health.

Locations

Harlingen, Texas, United States

Patients applied

0 patients applied

Trial Officials

Kelsey Baker

Principal Investigator

University of Texas Rio Grande Valley

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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