IMplementation of an RCT to imProve Treatment With Oral AntiCoagulanTs in Patients With Atrial Fibrillation

Stroke Clinical Trial

— IMPACT-AFib  

Official title:

IMplementation of a Randomized Controlled Trial (RCT) to imProve Treatment With Oral AntiCoagulanTs in Patients With Atrial Fibrillation

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03259373
• Other study ID #: IMPACT-AFib
• Status: Active, not recruiting
• Phase: N/A
• Start date: September 25, 2017
• Est. completion date: December 2021

Study information

• Verified date: December 2021
• Source: Harvard Pilgrim Health Care
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to use a decentralized claims database to determine whether education on stroke prevention in atrial fibrillation (AF) among AF patients and their providers can result in increased use of oral anticoagulants (OAC) for stroke prevention among those AF patients with guideline-based indications for oral anticoagulation (CHA₂DS₂-VASc score of 2 or greater). Specifically, the investigators will conduct a prospective, randomized, open-label education intervention trial to evaluate the effect of the early patient and provider education interventions on the proportion of patients with evidence of at least one OAC prescription fill (defined as one OAC dispensing or 4 international normalized ratio [INR tests] over the course of the follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time). A total of approximately 80,000 patients will be enrolled within multiple major health plans across the United States. The randomization will be performed by the central coordinating center, and the health plans will mail the educational intervention materials to their members and providers.

Description:

The study is a prospective, randomized, and open-label education intervention trial. Patients with AF and a CHA₂DS₂-VASc score of 2 or greater will be randomized in a 1:1 ratio to an intervention cohort and a control cohort within each participating health plan. The definition for OAC medication fill will be an OAC medication dispensing or at least 4 INR tests in the claims data. The claims records of the patients randomized to the intervention cohort will then be linked to "fresh" (i.e. about 1 month old) pharmacy claims data at the time of randomization. Patients without evidence of an OAC medication fill during the 12 months prior to randomization will be included in the patient-level and provider-level early educational intervention. In addition to usual care, these patients and their providers, where an individual provider may be identified, will receive a one-time mailing at trial start. Patients randomized to this early intervention with evidence of an OAC medication fill during the 12 months prior to randomization will be excluded from the trial. The control cohort will receive usual care over the initial study period. After the date on which at least 80% of eligible study participants have at least 12 months of follow-up time, "fresh" pharmacy claims data for the control intervention cohort that was generated and locked at the time of randomization will be used to assess trial eligibility, and those patients without evidence of an OAC medication fill during the 12 months prior to randomization will be included in the primary and secondary analyses as the control arm. Patients randomized to the control arm with evidence of an OAC medication fill during the 12 months prior to randomization will be excluded from the trial and will not be included in analyses. The baseline characteristics of the control patients will be examined at the same time point as the intervention patients, meaning at the time of randomization. The primary outcome is a comparison of the proportion of patients not on OAC during the 12 months prior to randomization, who were started on OAC over the course of the follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time in the early versus the delayed intervention arm. A total of approximately 80,000 patients (randomized 1:1) across all participating data partners (Aetna, Harvard Pilgrim, Humana, and Optum) will be enrolled from participating data partners across the United States. The follow-up time for the primary outcome will be 12 months from the date at which at least 80% of eligible study participates are enrolled (date on which early intervention materials are mailed). The providers of patients in the control cohort who did not receive OAC medication during the course of the 12-month study period and meet the inclusion criteria will receive the delayed intervention: the provider-only education intervention, a one-time mailing administered 12 months after at least 80% of early intervention mailings have occurred (patients will not receive any educational materials). The investigators intend to assess the primary and secondary endpoints again 24 months after at least 80% of early intervention mailings have occurred to assess the durability and longer-term outcomes of the effect of the patient- and provider-level education intervention, as well as the use of OAC following the delayed provider-level education intervention. However, as this second assessment is exploratory, investigators may not conduct these analyses if the results of the primary outcome are consistently null. Because the Sentinel Distributed Database will be used for follow-up information, and this information is refreshed approximately quarterly and this is done on separate timetables for the different health plans, it is likely that when at least the required follow-up time is available for at least 80% of people, there will be more than 12 or 24 months of followup for over 80% of people. All participants' outcomes will be assessed using all possible person-time; patients will have different duration of follow-up.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 64666
• Est. completion date: December 2021
• Est. primary completion date: September 30, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 30 Years and older

Eligibility

Inclusion Criteria:

1. Two or more diagnoses of AF (ICD-9 and/or 10 codes) at least one day apart and with at least one diagnosis within the last 12 months prior to the last date in the current approved data used for cohort identification

2. CHA2DS2-VASc score of 2 or greater

3. Medical and pharmacy insurance coverage of at least the prior year as identified via administrative claims databases of one of the participating data partners as of the date of randomization

4. Age 30 years or greater as of the last date in the current approved data used for cohort identification

Exclusion Criteria:

1. Evidence of OAC medication fill during the 12 months prior to randomization (determined at randomization for the early intervention cohort and 12 months post-randomization for the delayed intervention cohort)

2. Conditions other than AF that require anticoagulation, including treatment of deep venous thrombosis, pulmonary embolism, or ever having had a mechanical prosthetic heart valve prior to the last date in the current approved data used for cohort identification

3. Pregnancy within 6 months of the last date in the current approved data used for cohort identification

4. Any known history of intracranial hemorrhage prior to the last date in the current approved data used for cohort identification

5. Hospitalization for bleeding within the last 6 months of the last date in the current approved data used for cohort identification

6. Patients with recent P2Y12 antagonist use (i.e. clopidogrel, prasugrel, ticlopidine, or ticagrelor within 90 days of the last date in the current approved data used for cohort identification

Related Conditions & MeSH terms

• Atrial Fibrillation
• Stroke

Intervention

Behavioral:
• Early Patient-Level and Provider-Level Educational Intervention
Letters to patients that (1) explain to the patient that he or she appears to have AF, characterize the risk of stroke, and emphasize that although there may be a medical reason, the patient does not seem to be on an anticoagulant and (2) encourage the patient to discuss this with his or her provider to ask if he or she might benefit from OAC therapy to prevent stroke. Early intervention letters to providers explain this project, the nature of the problem, and identify a list of the provider's patients who have been contacted, as the provider and patient letters will be sent at approximately the same time; describe evidence and guidelines regarding oral anticoagulation.
• Delayed Provider-Level Educational Intervention
Delayed intervention letters to patients' providers, where they may be identified, that explain this project, the nature of the problem, and identify a list of their patients who are flagged as at risk for stroke and have not been treated with an oral anticoagulant; describe evidence and guidelines regarding oral anticoagulation.

Locations

Country	Name	City	State
United States	Aetna, Inc.	Blue Bell	Pennsylvania
United States	Humana Healthcare Research, Inc.	Louisville	Kentucky
United States	Harvard Pilgrim Health Care	Quincy	Massachusetts
United States	OptumInsight, Inc	Waltham	Massachusetts

Sponsors (7)

Lead Sponsor	Collaborator
Harvard Pilgrim Health Care	Aetna, Inc., Clinical Trials Transformation Initiative, Duke Clinical Research Institute, Food and Drug Administration (FDA), Humana Inc., OptumInsight Life Sciences, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of patients with evidence of at least one OAC dispensing (prescription fill) (defined as one OAC dispensing or 4 INR (International Normalized Ratio) tests)	Evaluate the effect of the patient and provider education interventions (versus usual care with delayed provider education intervention) on the proportion of patients with evidence of at least one OAC prescription fill (defined as one OAC dispensing or 4 INR tests) over the course of the 12 months of follow-up.	Follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time
Secondary	Rates of hospitalization for ischemic or unknown stroke	Evaluate the impact of the patient and provider education interventions on rates of ischemic / unknown stroke hospitalization	Follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time
Secondary	Rates of hospitalization for hemorrhagic stroke	Evaluate the impact of the patient and provider education interventions on rates of hospitalization for hemorrhagic stroke	Follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time
Secondary	Rates of hospitalization for ischemic or hemorrhagic stroke	Evaluate the impact of the patient and provider education interventions on rates of hospitalization for ischemic or hemorrhagic stroke	Follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time
Secondary	Rates of hospitalization for ischemic or hemorrhagic stroke or systemic embolism	Evaluate the impact of the patient and provider education interventions on rates of hospitalization for ischemic or hemorrhagic stroke or systemic embolism	Follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time
Secondary	Rates of hospitalization for ischemic or hemorrhagic stroke or systemic embolism or bleeding	Evaluate the impact of the patient and provider education interventions on rates of hospitalization for ischemic or hemorrhagic stroke or systemic embolism or bleeding	Follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time
Secondary	Rates of hospitalization for bleeding	Evaluate the impact of the patient and provider education interventions on rates of hospitalization for any bleeding	Follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time
Secondary	Time to first OAC dispensing	Evaluate the impact of the patient and provider education interventions on time to first OAC dispensing (prescription fill)	Follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time
Secondary	Proportion of days covered by OAC dispensing	Evaluate the impact of the patient and provider education interventions on proportion of days covered by OAC dispensings (prescription fills)	Follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time
Secondary	Proportion of patients on oral anticoagulation	Evaluate the impact of the patient and provider education interventions on proportion of patients on oral anticoagulation at 12 months of follow-up	Follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time
Secondary	All-cause in-hospital mortality rates	Evaluate the impact of the patient and provider education interventions on all-cause in-hospital mortality rates	Follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time
Secondary	Health care utilization for AF patients	Evaluate the impact of the patient and provider education interventions on health care utilization for AF patients, which would be reported as counts of number of health care utilization events (outpatient visits, days hospitalized, number of emergency department visits, etc.)	Follow-up through the date on which at least 80% of eligible study participants have at least 12 months of follow-up time

External Links

•   Sentinel Initiative IMPACT-AFib Project Page
•   White Paper: Developing Approaches to Conducting Randomized Trials Using the Mini-Sentinel Distributed Database