Implementing a Decision Support Tool to Prevent Community-Acquired Pressure Injury in Spinal Cord Injury (SCI) in the Spinal Cord Injury Clinic

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorVA Office of Research and Development

About this trial

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.

Eligibility criteria

Qualifiers

assigned provider in SCI clinic who is willing to participate in the study

has a scheduled appointment in the SCI clinic

ability to complete survey

Disqualifiers

active diagnosis of dementia

Trial design

Treatments tested in this trial

  • Provider training
  • CAPP-FIT intervention with RA facilitation
  • CAPP-FIT implementation during maintenance phase

Treatment groups

808 Participants
are divided into 3 treatment groups

Sponsors and collaborators

VA Office of Research and Development

Lead sponsor

VA Palo Alto Health Care System

Collaborator

VA Long Beach Healthcare System

Collaborator

Saint Louis VA Medical Center

Collaborator

James A. Haley Veterans' Hospital

Collaborator

Louis Stokes VA Medical Center

Collaborator

Michael E. DeBakey VA Medical Center

Collaborator

Iowa City Veterans Affairs Medical Center

Collaborator

San Diego Veterans Healthcare System

Collaborator

Edward Hines Jr. VA Hospital

Collaborator