Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
Healthy Volunteers
NCT05157282

Spinal Cord Stimulation for Functional Recovery in Humans With Tetraplegia

Led by VA Office of Research and Development · Updated on 2026-01-16

86

Participants Needed

2

Research Sites

209 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In support of the long-term goal of developing new strategies to increase limb function after SCI, the objectives of this proposal are to: 1) Examine the behavioral and physiological effects of TESS on upper-limb muscles after cervical SCI; and 2) Maximize the recovery of reaching and grasping potential by using tailored TESS in a task-specific manner with motor training. Veterans with cervical spinal injuries and healthy volunteers will be recruited for this study.

CONDITIONS

Official Title

Spinal Cord Stimulation for Functional Recovery in Humans With Tetraplegia

Who Can Participate

Age: 18Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female veterans aged 18 to 70 years
  • Chronic spinal cord injury of at least 1 year
  • Cervical spinal cord injury at C8 or above confirmed by MRI
  • Some preserved sensation in C6, C7, and C8 dermatomes
  • Able to make a visible power grip with one hand
  • Minimum score of 2 in cylindrical grasp on GRASSP test
  • For controls: males or females aged 18 to 70 years, right-handed, able to complete grasping tasks
Not Eligible

You will not qualify if you...

  • Uncontrolled pulmonary, cardiovascular, or orthopedic diseases
  • Debilitating diseases causing exercise intolerance prior to SCI
  • Major depression, psychosis, or altered cognitive status
  • History of head injury, concussion, skull fractures, recent unexplained headaches, or stroke
  • Presence of pacemaker or metal plate in skull
  • History of seizures
  • Use of drugs that lower seizure threshold such as certain antipsychotics or antidepressants
  • Pregnancy
  • Ongoing spinal cord compression, syrinx, or diseases like spinal stenosis, spina bifida, or herniated cervical disk

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Shirley Ryan AbilityLab

Chicago, Illinois, United States, 60611

Actively Recruiting

2

Edward Hines Jr. VA Hospital, Hines, IL

Hines, Illinois, United States, 60141-3030

Actively Recruiting

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Research Team

M

Monica A Perez, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

3

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