Skip to main content
Clinical Trials/NCT00328640
NCT00328640
Completed
Phase 4

Secondary Prevention After Ischemic Stroke: A Trial of an Evidence-Based System-Wide Intervention

University of California, San Francisco1 site in 1 country1,500 target enrollmentDecember 2005

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Ischemic Stroke
Sponsor
University of California, San Francisco
Enrollment
1500
Locations
1
Primary Endpoint
Medication utilization
Status
Completed
Last Updated
19 years ago

Overview

Brief Summary

Is a secondary prevention intervention, focused on implementation of standardized pre-printed discharge orders for hospitalists, effective at increasing utilization of the following evidence-based treatments 6 months after discharge for ischemic stroke:

  1. Treatment with statins,
  2. Control of hypertension, and
  3. Anticoagulation in patients with atrial fibrillation.

Detailed Description

There are several proven strategies for prevention of recurrent ischemic stroke, including use of statins, treatment of hypertension, and anticoagulation in patients with atrial fibrillation. Preliminary analyses suggest that only 9-15% of Kaiser Permanente Northern California's ischemic stroke patients receive optimal care for secondary prevention of stroke. The purpose of this study is to determine whether or not a quality improvement (QI) intervention can improve the care received by stroke patients. This project consists of a randomized trial of standardized stroke discharge order forms to improve adherence with best practices in secondary stroke prevention. The primary research question is: Is a secondary prevention intervention, focused on implementation of standardized pre-printed discharge orders for hospitalists, effective at increasing utilization of the following evidence-based treatments 6 months after discharge for ischemic stroke: (1) treatment with statins, (2) control of hypertension, and (3) anticoagulation in patients with atrial fibrillation. The primary outcome will be the proportion of patients receiving optimal treatment, as defined by these three goals. The impact of the intervention will be measures as a change after-to-before at intervention hospitals compared to non-intervention (control) hospitals, with the institution as the unit of analysis. Secondary analyses will evaluate the impact of the intervention on each of these components and on 6-month and 1-year rates of mortality, readmission for stroke, and costs of care after discharge.

Registry
clinicaltrials.gov
Start Date
December 2005
End Date
March 2007
Last Updated
19 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Ischemic stroke Kaiser-Permanente Health Plan Member with Pharmacy Benefit Discharged alive to home

Exclusion Criteria

  • tpA patients Hemorrhagic stroke TIA Significant comorbidities

Outcomes

Primary Outcomes

Medication utilization

Best Practices

Recurrent stroke

Secondary Outcomes

  • Mortality
  • Morbidity
  • Cost
  • Hospital readmission

Study Sites (1)

Loading locations...

Similar Trials