Using Practice Facilitation in Primary Care Settings to Reduce Risk Factors for Cardiovascular Disease

NCT02646488 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 276

Last updated 2019-05-20

No results posted yet for this study

Summary

The primary purpose of this study is to evaluate the effectiveness of practice facilitation as a quality improvement strategy for implementing the Million Hearts' ABCS treatment guidelines for reducing cardiovascular disease (CVD) among high-risk patients who receive care in primary care practices in New York City. The ABCS refer to the following: Aspirin in high-risk individuals (A), Blood pressure control and management (B), Cholesterol management (C), and Smoking cessation (S). The long-term goal is to create a robust infrastructure to disseminate and implement evidence based practice guidelines (EBPG) findings in primary care practices and improve practices' capacity to receive and implement other EBPG findings in the future.

Conditions

Interventions

BEHAVIORAL

Million Hearts ABCS 6 Months

The ABCS refer to the following: Aspirin in high-risk individuals (A), Blood pressure control and management (B), Cholesterol management (C), and Smoking cessation (S).

BEHAVIORAL

Million Hearts ABCS 9 Months

The ABCS refer to the following: Aspirin in high-risk individuals (A), Blood pressure control and management (B), Cholesterol management (C), and Smoking cessation (S).

BEHAVIORAL

Million Hearts ABCS 12 Months

The ABCS refer to the following: Aspirin in high-risk individuals (A), Blood pressure control and management (B), Cholesterol management (C), and Smoking cessation (S).

BEHAVIORAL

Million Hearts ABCS 15 Months

The ABCS refer to the following: Aspirin in high-risk individuals (A), Blood pressure control and management (B), Cholesterol management (C), and Smoking cessation (S).

BEHAVIORAL

Standard Care Regimen 9 Months

BEHAVIORAL

Standard Care Regimen 12 Months

BEHAVIORAL

Standard Care Regimen 15 Months

BEHAVIORAL

Standard Care Regimen 18 Months

BEHAVIORAL

Standard Care Regimen 21 Months

BEHAVIORAL

Standard Care Regimen 24 Months

BEHAVIORAL

Standard Care Regimen 27 Months

BEHAVIORAL

Follow Up Post Intervention 21 Months

BEHAVIORAL

Follow Up Post Intervention 24 Months

BEHAVIORAL

Follow Up Post Intervention 27 Months

BEHAVIORAL

Follow Up Post Intervention 30 Months

BEHAVIORAL

Follow Up Post Intervention 33 Months

Sponsors & Collaborators

  • Agency for Healthcare Research and Quality (AHRQ)

    collaborator FED
  • NYU Langone Health

    lead OTHER

Principal Investigators

  • Donna Shelley, MD · New York University Medical School

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-08-31
Primary Completion
2019-04-01
Completion
2019-04-01

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02646488 on ClinicalTrials.gov