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Effects of Coordinated Care for Disabled Medicaid Recipients

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00940511
Recruitment Status : Completed
First Posted : July 16, 2009
Last Update Posted : March 16, 2016
Information provided by (Responsible Party):

July 14, 2009
July 16, 2009
March 16, 2016
August 2009
January 2013   (Final data collection date for primary outcome measure)
Health care use through Medicaid [ Time Frame: Two years ]
Cost of care [ Time Frame: Two years ]
Complete list of historical versions of study NCT00940511 on ClinicalTrials.gov Archive Site
  • Primary and preventive care [ Time Frame: Six months, two years ]
  • Emergency department use [ Time Frame: Six months, two years ]
  • Hospital admissions [ Time Frame: Six months, two years ]
Same as current
Not Provided
Not Provided
Effects of Coordinated Care for Disabled Medicaid Recipients
Effects of Coordinated Care for Disabled Medicaid Recipients
The purpose of this study is to improve the quality of care for individuals with multiple chronic conditions, health care systems have begun turning to coordinated care. Although coordinated care can refer to many different things, it usually includes activities such as assessing patients' needs, referring them to the right doctors, helping them make and keep appointments, and helping them comply with medical or dietary recommendations. To understand the effects of coordinated care for high-needs Medicaid recipients, MDRC is conducting a randomized trial of a pilot coordinated care program run by Kaiser Permanente for blind and disabled Medicaid recipients in the Denver area.
Not Provided
Not Provided
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Chronic Conditions Faced by Medicaid Recipients With Disabilities
Behavioral: Coordinated care
  • Experimental: Coordinated care
    Individuals will be passively enrolled in Medicaid managed care. Those who do not opt out of managed care will be provided with care coordination.
    Intervention: Behavioral: Coordinated care
  • No Intervention: Usual care
    The usual care group will remain in fee-for-service Medicaid and receive services normally available through that system.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
January 2013
January 2013   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Disabled, in fee-for-service Medicaid

Exclusion Criteria:

  • Under age 18, over age 64
Sexes Eligible for Study: All
18 Years to 65 Years   (Adult)
Contact information is only displayed when the study is recruiting subjects
United States
Not Provided
Plan to Share IPD: No
Charles Michalopoulos, MDRC
  • Center for Health Care Strategies
  • Robert Wood Johnson Foundation
  • Colorado Department of Health Care Policy and Financing
  • Kaiser Permanente
Principal Investigator: Charles Michalopoulos, Ph.D. MDRC
March 2016

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