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Clinical Trials/NCT02569528
NCT02569528
Completed
Not Applicable

ImplemeNtation oF demOnstration pRoject for Health systeMs: Atrial Fibrillation (INFORM-AF) Part 1

Duke University1 site in 1 country52 target enrollmentOctober 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Atrial Fibrillation
Sponsor
Duke University
Enrollment
52
Locations
1
Primary Endpoint
Perceptions of using anticoagulation as a stroke prevention therapy in atrial fibrillation, as measured by survey and interview
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The goal of this study is to learn about the patient and provider perceptions, priorities, preferences, and willingness to use/prescribe anticoagulation as a stroke prevention therapy in patients with atrial fibrillation. Qualitative interviews will be performed with atrial fibrillation patients and providers caring for atrial fibrillation patients. The investigators want to understand the factors that influence decision-making about anticoagulation medications, and to gain insight into patients' and providers' knowledge of the risk of stroke and bleeding associated with oral anticoagulation. This feedback will help provide better education to providers caring for patients with atrial fibrillation and better care to patients with atrial fibrillation by developing tools to optimize the appropriate use of oral anticoagulation for patients with atrial fibrillation.

Registry
clinicaltrials.gov
Start Date
October 2015
End Date
March 2, 2017
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • adult patient age 18 or older;
  • English speaking;
  • diagnosed atrial fibrillation;
  • at least 1 risk factor for congestive heart failure, hypertension, age, diabetes, stroke (CHADS2) or 2 risk factors for CHADS2 with vascular disease, age, and sex (CHADS2-VASc) ;
  • no documented cognitive impairment per the medical record;
  • not being prescribed an oral anticoagulant
  • Provider Inclusion Criteria:
  • physician at one of the study sites treating patients diagnosed with atrial fibrillation

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Perceptions of using anticoagulation as a stroke prevention therapy in atrial fibrillation, as measured by survey and interview

Time Frame: one hour

Each telephone interview (data collection time point) will be approximately one hour

Secondary Outcomes

  • Willingness to use anticoagulation as a stroke prevention therapy in atrial fibrillation, as measured by survey and interview(one hour)
  • priorities for using anticoagulation as a stroke prevention therapy in atrial fibrillation, as measured by survey and interview(one hour)
  • preferences for using anticoagulation as a stroke prevention therapy in atrial fibrillation, as measured by survey and interview(one hour)

Study Sites (1)

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