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RecruitingSpinal Cord Injuries

Remote Ischemic Conditioning for PwSCI

Eligible age

18+ yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

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About this study

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.

Sponsor: Washington University School of Medicine

You may qualify if…

  • 18 years of age or older
  • Diagnosis of SCI
  • Live within the community (not nursing facility)
  • Not actively engaged in physical activity for exercise
  • Not having the ability to participate in physical activity due to physical capacity or environmental barriers
  • Medically stable
  • Ability to obtain physician approval to participate in the study
  • Willingness to participate in a 2-day initial assessment visit at research testing location, 30 intervention sessions conducted independently by the participant or caregivers, 2-day post intervention assessment visit at research testing location.

You may not qualify if…

  • Medically unstable
  • Have had a heart-related condition within the past year
  • Have had a blood clot in the past year
  • Have a stage 3 or 4 pressure injury
  • Have taken blood thinners in the past year
  • Have had surgery in the past year
  • Have uncontrolled hypertension
  • Have peripheral artery disease

Where it's recruiting

Missouri

St Louis

Source: ClinicalTrials.gov · NCT07488793 · last updated 2026-03-23