Assessing the Effectiveness of Concurrent Peer Review for Patients With Cardiovascular Disease and Diabetes

This study has been completed.
Sponsor:
Collaborator:
Robert Wood Johnson Foundation
Information provided by (Responsible Party):
Kevin Fiscella, University of Rochester
ClinicalTrials.gov Identifier:
NCT00508014
First received: July 25, 2007
Last updated: November 30, 2011
Last verified: November 2011

July 25, 2007
November 30, 2011
December 2006
June 2010   (final data collection date for primary outcome measure)
Mean change in blood pressure, glycated hemoglobin, and LDL-cholesterol between baseline and follow-up [ Time Frame: 7 months ] [ Designated as safety issue: No ]
Mean change in blood pressure, glycated hemoglobin, and LDL-cholesterol between baseline and follow-up [ Time Frame: 7 months ]
Complete list of historical versions of study NCT00508014 on ClinicalTrials.gov Archive Site
Use of aspirin, ACE inhibiters/ARBs (diabetic patients), pneumonia vaccine updated, diabetic foot exam, diabetic microalbumuria check, retinal exam, smoking cessation counseling, dental visit, and self management goal [ Time Frame: one year ] [ Designated as safety issue: No ]
Use of aspirin, ACE inhibiters/ARBs (diabetic patients), pneumonia vaccine updated, diabetic foot exam, diabetic microalbumuria check, retinal exam, smoking cessation counseling, dental visit, and self management goal [ Time Frame: one year ]
Not Provided
Not Provided
 
Assessing the Effectiveness of Concurrent Peer Review for Patients With Cardiovascular Disease and Diabetes
Concurrent Peer Review Visits to Reduce Cardiovascular Risk Factors

We will assess the impact of concurrent peer review vists on blood pressure, cholesterol and diabetes control. Concurrent peer review (CPR) visits refer to special offic visits by patients to a clinician (physician, nurse practitioner, or physician assistant) other than than their primary care provider that are specifically designed to improve care for diabetes and cardiovascular disease.

This project aims to reduce racial and ethnic disparities in health care by improving cardiovascular and diabetes management among poor and minority patients. We propose to implement and evaluate an innovative, but practical intervention: CPR visits. CPR visits are designed to minimize competing demands for clinicians and reduce clinical inertia by focusing clinician and patient attention on optimizing cardiovascular and/or diabetes management and disease control and through use of clinician prompts and decision support at the point of care. Following training of clinician staff, CPR visits will be implemented within two sites of a single community health center (Westside Health Services, Inc). Patients will be randomly assigned one CPR visit with a clinician other than their primary care clinician or to usual care. The primary study outcome will include control of hypertension, diabetes, and lipids. Secondary outcomes will include process measures for cardiovascular and diabetes care. Both personnel and data collection infrastructure will build on the existing Health Disparities Collaborative at Westside. A research team from the University of Rochester will assist in the implementation of study design. This team will lead both the quantitative and qualitative evaluation of the project including outcome and process measures. Project findings offer promise for improving care to underserved populations through dissemination and implementation of a feasible strategy among practices caring for the underserved. Findings will be disseminated nationally in conjunction with the Robert Wood Johnson Foundation, the National Association of Community Health Centers, and the National Health Disparities Collaborative and through publication in the peer reviewed literature and presentation at national conferences.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Health Services Research
Cardiovascular Diseases
  • Other: Usual Care
    Usual Care with primary care provider during time period
  • Behavioral: Usual Care
    One CPR visit
  • No Intervention: Control
    usual care
    Intervention: Other: Usual Care
  • Experimental: CPR visit
    Receipt of CPR visit
    Intervention: Behavioral: Usual Care
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
727
June 2010
June 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Active patient at Westside Health Services.
  • Currently enrolled in the Health Disparities Collaborative at WHS.
  • At least one visit to primary care provider in past year.
  • Any of the following documented during the preceding three months:
  • BP not at goal e,g. (BP 140/80 or greater unless has DM, CAD or CRI then BP greater than 130/80), LDL-C not at goal (level dependent on absolute ATP III CVD risk) or glycated hemoglogin 7 percent or higher

Exclusion Criteria:

  • Less than 18 years of age
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00508014
59768
No
Kevin Fiscella, University of Rochester
University of Rochester
Robert Wood Johnson Foundation
Study Director: Kevin Fiscella, MD, MPH University of Rochester
University of Rochester
November 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP