Protocol-guided Rapid Evaluation of Veterans Experiencing New Transient Neurological Symptoms "PREVENT"

Enrolling by invitation

Phase N/A Results N/A

Trial Description

This program will seek to implement a quality improvement program to improve the care of Veterans with TIA or minor stroke at 6 Veteran Health Administration Hospitals. The investigators will evaluate the implementation and effectiveness of the quality improvement program.

Detailed Description

Aim 1. To develop a quality improvement program to improve the care of Veterans with TIA or minor stroke that can be deployed nationwide. The program will include multiple components: a reporting system that is based on validated electronic quality measures (eCQMs) that will allow staff to monitor the time-sensitive processes of care and outcomes of their population of Veterans with TIA or minor stroke; clinical protocols to improve the timeliness and completeness of care; professional education materials; and clinical note templates for use by nursing and pharmacy staff. Lessons learned at the individual sites engaged in the quality improvement program will be shared across sites by use of a web-based platform and a virtual collaborative.
Aim 2. To evaluate the effectiveness of the Aim 1 QI intervention program for Veterans with TIA or minor stroke against usual care. Teams at the 6 intervention sites will be given the quality improvement program components. The primary effectiveness outcome is the proportion of Veterans who received all of the guideline-concordant processes of care for which they are eligible referred to as the "Without-Fail" care rate. The secondary effectiveness outcome is the 90-day recurrent vascular event rate.
Aim 3. To evaluate the implementation of the QI intervention program across the 6 participating sites. The implementation outcomes will be: participating clinician satisfaction with the quality improvement program; participating staff members' assessment of the quality improvement program components including the eCQM and the web-based platform in terms of usability, complexity, and relative advantage; and the adaptability of the program over the course of the study.
Aim 4. To evaluate CFIR constructs and contextual factors associated with successful and suboptimal implementation of this new program for Veterans with an acute medical problem requiring timely care.
Secondary Aim To evaluate the sustainability of the program. Sustainability will be evaluated over a one-year period that begins immediately after the one-year active implementation period.

Conditions

Interventions

  • Quality Improvement Program Other
    Other Names: QI Intervention
    Intervention Desc: The Intervention is a QI Program that will include multiple components as described above.
    ARM 1: Kind: Experimental
    Label: QI with External Facilitation
    Description: Receive external facilitation to support implementation of the quality improvement program

Trial Design

  • Allocation: Randomized
  • Masking: Open Label
  • Purpose: Health Services Research
  • Intervention: Factorial Assignment

Outcomes

Type Measure Time Frame Safety Issue
Primary Implementation: Eligible Veterans enrollment- direct count During One Year of active implementation No
Primary Effectiveness: Defect-free care rate Over the course of One Year active implementation No
Primary Effectiveness: Recurrent vascular event rate During one year after patient enrolls No
Secondary Sustainability: Eligible Veterans enrollment Over a one-year period that begins immediately after the one-year active implementation period No
Primary Effectiveness: Without-fail care rate Over the course of One Year active implementation

Sponsors