Richmond, VANCT05423600Now EnrollingIRB Ready

Tetraplegia/Tetraparesis Clinical Trial in Richmond, VA

Access cutting-edge tetraplegia/tetraparesis treatment through this clinical trial at a research site in Richmond. Study-provided care at no cost to qualified participants.

Sponsored by Virginia Commonwealth University

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Expert Care in Richmond

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IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related tetraplegia/tetraparesis treatment provided free

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Check if you qualify for this tetraplegia/tetraparesis clinical trial in Richmond, VA

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Why Participate?

  • No-Cost Study Care

  • Local to Richmond

    Convenient for VA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Richmond site if eligible
  4. 4Begin participation

About This Tetraplegia/Tetraparesis Study in Richmond

The purpose of the current study is to evaluate whether a home-based, telehealth-supported intervention combining Blood Flow Restricted Exercise (BES) and Transspinal Stimulation (TS) will improve motor and functional abilities greater than BES+sham TS in persons with chronic, incomplete tetraplegia.

Sponsor: Virginia Commonwealth University

Who Can Participate

Inclusion Criteria

A written clearance from the study medical doctor to ensure that the participant is safely able to engage in the study.
Participants must have a companion that will be able to help him/her throughout the study.
Greater than 1-year post SCI, neurologic level of C8 or above.
American Spinal Injury Association Impairment Scale (AIS) scores of B, C, or D indicating presence of an incomplete SCI.
Visible muscle contraction response to NMES wrist extensors, bilaterally.
Agreement to use telehealth services for delivery of research exercise training by study staff. Possesses appropriate technology to engage in telehealth including a personal web camera, computer, microphone, speakers, and high-speed broadband internet connection, valid email address (needed to obtain VA issued video conferencing software), and telephone number used to obtain login credentials for the In-Home Video Software - Cisco Jabber Video for Telepresence Software.
Response of muscle contraction of wrist extensors bilaterally to neuromuscular electrical stimulation.

Exclusion Criteria

Unhealed fracture in upper or lower extremities.
Severe scoliosis, severe upper extremity contractures, or other musculoskeletal issues that would impede participation in a BES + TS intervention or valid evaluation of outcome measures.
High resting blood pressure greater than 140/80 mmHg.
Taking anti-coagulants or anti-platelet agents, including aspirin if unable to be off this medication for medical reasons.
Pregnancy (female participants). A home pregnancy test will be conducted to role out any pregnancy before the study at the McGuire VAMC. The test will be repeated every month during the course of the study.
Implanted pacemakers and/or implanted defibrillator devices.
Other exclusion criteria may include the presence of implanted electrical device, cancer, thrombosis, pacemaker, defibrillator, or seizures. Patients who are currently on or receive anti-platelet or anticoagulant medications will be excluded from the trial.
Any condition that, in the judgment of the principal investigator or medical provider, precludes safe participation in the study.
Other exclusion criteria at the discretion of the medical team may include:
Uncontrolled autonomic dysreflexia (AD), refers to episodes of AD that do not respond to medications to ensure stable blood pressure in persons with SCI
Concurrent severe neurological injuries other than SCI: MS, CP, severe TBI, and stroke.
Unresolved deep vein thrombosis.
Psychiatric or cognitive impairments that preclude adherence to the intervention.
Known cardiac pathology that precludes safe participation.
Metabolic conditions such as cardiovascular disease, uncontrolled type II diabetes mellitus, uncontrolled hypertension, and those on insulin.
Presence of pressure sores stage three or greater.
Presence of a symptomatic urinary tract infection.
Severe spasticity as assessed by the Modified Ashworth Scale.
Changing neurologic status due to conditions such as progressive posttraumatic syringomyelia.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Richmond?

Yes, this clinical trial (NCT05423600) has an active research site in Richmond, VA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Tetraplegia/Tetraparesis Treatment Options in Richmond, VA

If you're searching for tetraplegia/tetraparesis treatment options in Richmond, VA, this clinical trial (NCT05423600) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Richmond research site is actively enrolling participants for this clinical trial. You'll receive care from experienced tetraplegia/tetraparesis specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all tetraplegia/tetraparesis clinical trials near you to find additional studies recruiting in your area.

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