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Assessing the Effectiveness of Concurrent Peer Review for Patients With Cardiovascular Disease and Diabetes
This study is currently recruiting participants.
Verified by University of Rochester, July 2007
Sponsors and Collaborators: University of Rochester
Robert Wood Johnson Foundation
Information provided by: University of Rochester
ClinicalTrials.gov Identifier: NCT00508014
  Purpose

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.


Condition Intervention
Cardiovascular Diseases
Other: Usual Care
Behavioral: Active

MedlinePlus related topics: Cholesterol Diabetes
U.S. FDA Resources
Study Type: Interventional
Study Design: Health Services Research, Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study
Official Title: Concurrent Peer Review Visits to Reduce Cardiovascular Risk Factors

Further study details as provided by University of Rochester:

Primary Outcome Measures:
  • Mean change in blood pressure, glycated hemoglobin, and LDL-cholesterol between baseline and follow-up [ Time Frame: 7 months ]

Secondary Outcome Measures:
  • 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 ]

Estimated Enrollment: 750
Study Start Date: December 2006
Estimated Study Completion Date: November 2008
Arms Assigned Interventions
CONTROL: Active Comparator
usual care
Other: Usual Care
Usual Care with primary care provider during time period
ACTIVE: Experimental
Receipt of CPR visit
Behavioral: Active
One CPR visit

Detailed Description:

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.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00508014

Contacts
Contact: Ellen Volpe, FNP, RN 585-436-3040 Ellen_Volpe@urmc.rochester.edu
Contact: Trish Harren, MA 585-436-3040 Tharren@westsidehealth.net

Locations
United States, New York
Westside Health Services, Inc Recruiting
Rochester, New York, United States, 14611
Principal Investigator: Ellen Volpe, FNP, RN            
Sponsors and Collaborators
University of Rochester
Robert Wood Johnson Foundation
Investigators
Study Director: Kevin Fiscella, MD, MPH University of Rochester
  More Information

Robert Wood Johnson Foundation Website on Grantees  This link exits the ClinicalTrials.gov site

Study ID Numbers: 59768
Study First Received: July 25, 2007
Last Updated: July 26, 2007
ClinicalTrials.gov Identifier: NCT00508014  
Health Authority: United States: Institutional Review Board

Keywords provided by University of Rochester:
Cardiovascular disease
Diabetes
Quality improvement
Peer review

Study placed in the following topic categories:
Diabetes Mellitus

Additional relevant MeSH terms:
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 16, 2009