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NCT06529094 · ClinicalTrials.gov registry record · NA
Implementing a Decision Support Tool to Prevent Community-Acquired Pressure Injury in Spinal Cord Injury (SCI) in the Spinal Cord Injury Clinic
A NA study of Spinal Cord Injury and Pressure Injury, sponsored by VA Office of Research and Development.
- Recruiting
- Registry status
- NA
- Development phase
- 808
- Enrollment target
- 7
- Study locations
NCT06529094 is a NA study of Spinal Cord Injury and Pressure Injury that is actively recruiting participants, run by VA Office of Research and Development. The registered enrollment target is 808 participants, above the 78-participant average among 99 other Spinal Cord Injury trials with a reported enrollment target (936% higher). The trial reports 7 study locations across 6 states.
The verdict
NCT06529094, a NA study of Spinal Cord Injury and Pressure Injury, is actively recruiting participants, sponsored by VA Office of Research and Development.
- RECRUITING
- Registry status
- NA
- Development phase
- 808 participants
- Enrollment target
- 7
- Study locations
Study Summary
Spinal cord injury (SCI) is a permanent condition affecting every aspect of life including health, daily activities, and participation and quality of life. Persons with SCI are at high risk of pressure injury (PrI) throughout their lives due to loss of sensation, nerve damage and immobility. PrIs are local areas of damage to the skin and underlying soft tissue caused by pressure and shear commonly located over bony prominences. While most PrIs are hospital- or nursing home-acquired, in people with SCI, PrIs typically develop in the community. Community-acquired pressure injuries (CAPrIs) are common, devastating, and costly. This grant proposal will assess how well a decision support tool, called the Community Acquired Pressure Injury Prevention Field Implementation Tool (CAPP-FIT), is used in the clinic and how well it prevents CAPrIs. The CAPP-FIT will be implemented at seven sites across the country in a staggered fashion. The CAPP-FIT includes: 1) an automated Veteran survey to identify risks, actions, and resources needed to prevent CAPrIs and 2) a companion Provider Report immediately available in the electronic health record listing Veteran responses to survey items with recommended evidence-based provider actions. The Veteran survey can be completed via a secured email on the computer or phone. There are three aims in the proposal: Aim 1 is implementing the CAPP-FIT at the seven geographically diverse VA SCI clinics. After CAPP-FIT implementation, each site will determine how the CAPP-FIT will be maintained in clinical practice to support sustainability. Aim 2 assesses how well the CAPP-FIT prevents CAPrIs and CAPrI-associated hospitalizations and assesses provider and Veteran satisfaction. Aim 3 assesses how well the CAPP-FIT is implemented in the SCI clinic.
Conditions Studied
Interventions
- BEHAVIORAL Provider training
- BEHAVIORAL CAPP-FIT intervention with RA facilitation
- BEHAVIORAL CAPP-FIT implementation during maintenance phase
Study Locations (7)
California
- VA Long Beach Healthcare System, Long Beach, CA - Long Beach
- VA Palo Alto Health Care System, Palo Alto, CA - Palo Alto
Florida
- James A. Haley Veterans' Hospital, Tampa, FL - Tampa
Illinois
- Edward Hines Jr. VA Hospital, Hines, IL - Hines
Missouri
- St. Louis VA Medical Center John Cochran Division, St. Louis, MO - St Louis
Ohio
- Louis Stokes VA Medical Center, Cleveland, OH - Cleveland
Texas
- Michael E. DeBakey VA Medical Center, Houston, TX - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 808 participants |
| Start Date | 2024-11-01 |
| Est. Completion | 2028-07-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06529094
The ClinicalTrials.gov registry entry for NCT06529094 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 808 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 78-participant average among 99 other Spinal Cord Injury trials with a reported enrollment target (936% higher). The listed sponsor is VA Office of Research and Development, which has 1,668 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Spinal Cord Injury appearing as the primary indexed condition, and to 3 interventions - of which Provider training is the first listed.
NCT06529094 reports 7 study locations spanning 6 distinct geographic areas - top geographies include California, Florida, Illinois.
Frequently Asked Questions
What is clinical trial NCT06529094 about?
NCT06529094 is a clinical study titled "Implementing a Decision Support Tool to Prevent Community-Acquired Pressure Injury in Spinal Cord Injury (SCI) in the Spinal Cord Injury Clinic". Spinal cord injury (SCI) is a permanent condition affecting every aspect of life including health, daily activities, and participation and quality of life. Persons with SCI are at high risk of pressure injury (PrI) throughout their lives due to loss of sensation, nerve damage and immobility. PrIs ar...
What is the current status of trial NCT06529094?
This trial is currently recruiting. It is a NA study. The enrollment target is 808 participants. The study started on 2024-11-01. Estimated completion is 2028-07-31.
What conditions does trial NCT06529094 study?
This clinical trial studies the following conditions: Spinal Cord Injury, Pressure Injury.
What interventions are being tested in trial NCT06529094?
The interventions under investigation include: Provider training (BEHAVIORAL), CAPP-FIT intervention with RA facilitation (BEHAVIORAL), CAPP-FIT implementation during maintenance phase (BEHAVIORAL).
Who is sponsoring clinical trial NCT06529094?
This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06529094 being conducted?
This trial has 7 study locations across California, Florida, Illinois, Missouri, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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