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Evaluation of Programs of Coordinated Care and Disease Management

Not Applicable
Conditions
Diabetes
Chronic Obstructive Pulmonary Disease
Major Depression
Congestive Heart Failure
Psychotic Disorder
Cerebrovascular Disease
Cancer
Coronary Artery Disease
Alzheimer's Disease
Interventions
Behavioral: Care Coordination
Registration Number
NCT00627029
Lead Sponsor
Mathematica Policy Research, Inc.
Brief Summary

This is a Congressionally mandated study. In the original study, 16 demonstration programs provided care coordination services to beneficiaries with chronic illness in Medicare's fee-for-service program. A five-year CMS-funded study tested whether the programs can improve patients' use of medical services, improve patients' outcomes and satisfaction with care, and reduce Medicare costs. The study also assessed physicians' satisfaction with the programs.

In 2008 Congress extended the project for two of the original programs--Mercy Medical Center - North Iowa and Health Quality Partners in Pennsylvania--and they will enroll Medicare beneficiaries and provide care coordination services into the spring of 2010.

Detailed Description

Mathematica Policy Research, Inc. (MPR) evaluated 16 independent demonstration sites that provide coordinated care interventions to Medicare beneficiaries with chronic illnesses. The rationale for the demonstration is the lack of coordination among the multiple providers typically serving Medicare beneficiaries with chronic illnesses, as well as the adverse consequences of the lack of coordination for the beneficiaries and for Medicare costs. The demonstration sites, selected in early 2001, offered programs designed to improve both the care that patients receive and patients' knowledge of, and adherence with, recommended self-care and behavior. The study estimated the effects of each site on patients' well-being and satisfaction, in addition to the site's effects on the use and cost of Medicare covered services. This analysis relied on a patient survey conducted 6 to 12 months after enrollment, and on Medicare claims data and any data available from the demonstration sites that could enhance the study. The study included two rounds of physician surveys. In each site, eligible applicants were randomly assigned to treatment and control groups. An extensive process analysis was conducted to describe the interventions in detail, with the key goal being an assessment of those factors that account for program success and failure. The study included case studies of each site, program profiles, interim site-specific memos, two interim summary reports, two reports to Congress (based on the interim summary reports), and a final summary report. This original study enrolled 18,277 beneficiaries.

In 2008 Congress extended the study for 2 of the sites, Mercy Medical Center - North Iowa and Health Quality Partners in Pennsylvania, and they will recruit beneficiaries and provide demonstration intervention services through the spring of 2010. Mathematica Policy Research will evaluate the results of this extended demonstration using Medicare claims data and qualitative site visits to the two programs.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
18277
Inclusion Criteria
  • Meets clinical and prior health service use criteria of each of the 16 demonstration sites (vary across demonstration programs)
  • Resides in catchment area of one of the programs
  • Enrolled in Medicare fee-for-service program
  • Coverage by both Medicare Parts A and B
  • Medicare is primary payer
Exclusion Criteria
  • Does not meet any of the relevant program's exclusion criteria (vary across demonstration programs)
  • Not enrolled in a Medicare Advantage plan (Medicare managed care program)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionCare CoordinationCare coordination, consisting variously (depending on the demonstration site)--nurse telephonic counseling, nurse in-person home visits, home telemonitoring equipment, and physician education and feedback.
Primary Outcome Measures
NameTimeMethod
Medicare program expendituresEight years
Secondary Outcome Measures
NameTimeMethod
Claims-based and patient-reported quality of careEight years

Trial Locations

Locations (15)

CorSolutions/Matria Healthcare

🇺🇸

Rosemont, Illinois, United States

Medical Care Development

🇺🇸

Augusta, Maine, United States

Charlestown/Erickson Retirement Communities

🇺🇸

Catonsville, Maryland, United States

University of Maryland Medical Center

🇺🇸

Baltimore, Maryland, United States

Georgetown University Medical Center-Mind My Heart Program

🇺🇸

Washington, District of Columbia, United States

Carle Foundation and Hospital

🇺🇸

Urbana, Illinois, United States

Washington University-St.Louis School of Medicine/Barnes-Jewish Hospital

🇺🇸

St. Louis, Missouri, United States

Jewish Home Lifecare

🇺🇸

New York, New York, United States

Lovelace Health Systems

🇺🇸

Albuquerque, New Mexico, United States

Hospice of the Valley MediCaring Project

🇺🇸

Phoenix, Arizona, United States

Quality Oncology/Matria Healthcare

🇺🇸

Sunrise, Florida, United States

Mercy Medical Center - North Iowa

🇺🇸

Mason City, Iowa, United States

Avera McKennan Hospital and University Health Center

🇺🇸

Sioux Falls, South Dakota, United States

QMed, Inc.

🇺🇸

Eatontown, New Jersey, United States

CenVaNet

🇺🇸

Richmond, Virginia, United States

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