24 Participants NeededMy employer runs this trial

Remote Ischemic Conditioning for Spinal Cord Injury

W
KA
Overseen ByKerri A Morgan, PhD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Washington University School of Medicine

What You Need to Know Before You Apply

What is the purpose of this trial?

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 Is on the Research Team?

KA

Kerri A Morgan, PhD

Principal Investigator

Washington University School of Medicine - Program in Occupational Therapy

Are You a Good Fit for This Trial?

Inclusion Criteria

* Medically stable
* Ability to obtain physician approval to participate in the study
I am 18 years old or older.
See 5 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2 days
2 visits (in-person)

Treatment

Participants undergo a 6-week remote ischemic conditioning (RIC) intervention at home, with daily logs of sessions

6 weeks
Home-based intervention

Post-assessment

Participants complete a 2-day post-assessment to evaluate cardiometabolic health outcomes

2 days
2 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

2 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • RIC

How Is the Trial Designed?

3

Treatment groups

Active Control

Placebo Group

Group I: Remote ischemic conditioning (RIC) high-dose using the automated blood flow restriction cuffActive Control1 Intervention
Group II: Remote ischemic conditions (RIC) high-dose using standard blood pressure cuffActive Control1 Intervention
Group III: Remote ischemic conditioning (RIC) low-dose using standard blood pressure cuffPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Washington University School of Medicine

Lead Sponsor

Trials
2,027
Recruited
2,353,000+

The Craig H. Neilsen Foundation

Collaborator

Trials
62
Recruited
3,100+