Remote Ischemic Conditioning for PwSCI (NCT07488793)
Remote Ischemic Conditioning Intervention to Enhance the Cardiometabolic Health of Persons With SCI
๐ฉบ Plain-English Summary (8th-Grade Level)
The long-term goal of this project is to improve the overall cardiometabolic health of persons with spinal cord injury (SCI). This pilot study will test the feasibility and acceptability of remote ischemic conditioning implemented in a home setting by persons with SCI and collect cardiometabolic health outcomes to inform appropriate outcomes for a future larger trial. Researchers will compare, RIC high dose using standard blood pressure cuff to RIC high dose using automated blood flow restriction cuff to RIC low dose using standard blood pressure cuff, to determine cardiometabolic health improvements amongst groups. Participants will: Complete an initial 2-day assessment, participate in a 6-week intervention using remote ischemic conditioning (RIC) within their home, complete a 2-day post assessment.
Who can join: Review the eligibility criteria below.
Location: Washington University School of Medicine โ St Louis, Missouri
Age range: 18 Years
๐งช Interventions in This Study
- RIC high-dose standard blood pressure cuff (BEHAVIORAL)
- RIC high-dose automated blood flow restriction cuff (BEHAVIORAL)
- RIC low-dose standard blood pressure cuff (BEHAVIORAL)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- Washington University School of Medicine โ St Louis, Missouri
๐ Contact the Study Coordinator
Phone: (314) 286-1659
Email: morgank@wustl.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Spinal Cord Injuries
- Use of Point-of-care Neuro-sacral Electrophysiology Following Spinal Cord Injury โ Montreal, Quebec
- Wearable Electrical Stimulation on the Back to Modulate Spinal Cord Activity โ Philadelphia, Pennsylvania
- SCIVAX: Biomarkers of Immune Dysfunction and Vaccine Responsiveness in Chronic SCI โ Manhasset, New York
- Autologous Adipose Derived Mesenchymal Stem Cells for Spinal Cord Injury Patients โ Rochester, Minnesota
- Standing, Stepping and Voluntary Movement Spinal Cord Epidural Stimulation โ Louisville, Kentucky
- Acute Intermittent Hypoxia on Leg Function Following Spinal Cord Injury โ Cambridge, Massachusetts
Explore by condition: All Spinal Cord Injuries clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.