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Clinical Trials/NCT01014884
NCT01014884
Terminated
Not Applicable

Coventry Outcomes Study of Seniors: A Dual-arm, Controlled, Randomized, Comparative Effectiveness Study to Evaluate the Effect of a Multidisciplinary Team's Intervention Versus Usual Care on the Incidence of Nonelective Hospitalizations in a Medicare Population

Medco Health Solutions, Inc.0 sites2,150 target enrollmentNovember 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Failure
Sponsor
Medco Health Solutions, Inc.
Enrollment
2150
Primary Endpoint
Determine the impact of multidisciplinary team interventions in reducing the rate of non-elective hospitalizations over a 12 month period compared to usual care
Status
Terminated
Last Updated
16 years ago

Overview

Brief Summary

The investigators are studying the impact of the interventions of a multidisciplinary team (MDT) - consisting of a Coventry case manager, social worker, and medical director, alongside a Medco specialist pharmacist - on the hospitalization rates of high risk seniors with chronic conditions, compared with a usual care approach. The study will also examine the impact on quality of life, medication adherence, medical costs, hospital readmission rates, and a variety of other important measures. The outcome of COSS may support a means to further enhance and develop a comprehensive care model program by leveraging the partnership between a health plan and a pharmacy benefit manager.

Detailed Description

The multidisciplinary team will provide face-to-face visits in a home setting with interventions that focus on five key areas: care transitions, self-management, care coordination, pharmacy and prevention, all designed to support high-risk Medicare members and their relationship with their primary care providers. If the study proves to reduce hospitalizations in the senior population, it could provide important guidance for future efforts to reduce the cost and improve the quality of care for seniors with chronic conditions.

Registry
clinicaltrials.gov
Start Date
November 2009
End Date
June 2011
Last Updated
16 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Inouye Risk Score \>3 calculated on Coventry Claims
  • Medicare Advantage beneficiaries age \> 65 years
  • Continuous eligibility \> 12 months prior to study
  • Ability to be contacted via telephone
  • Subject is willing and able to provide informed consent
  • Willing to comply with all study procedures and be available for the duration of the study

Exclusion Criteria

  • Active cancer treatment (i.e. chemotherapy or radiation) in the past 6 months
  • Living anywhere other than a community setting \[i.e. Skilled nursing facility (SNF)\]
  • Just-In-Time (JIT) Members
  • Members with a geographic location \> 60 from either St. Louis or Kansas City, MO.
  • Solid organ transplant recipients
  • Active enrollment in another clinical research study

Outcomes

Primary Outcomes

Determine the impact of multidisciplinary team interventions in reducing the rate of non-elective hospitalizations over a 12 month period compared to usual care

Time Frame: 12 months

Secondary Outcomes

  • Determine the impact of multidisciplinary team interventions on the rate of emergency room visits not resulting in hospitalization in a 24 hour period or less.(12 months)
  • Determine the impact of multidisciplinary team interventions versus usual care on health-related quality of life (HR-QOL)(12 months)
  • Determine the impact of MDT interventions versus usual care on inpatient costs associated with non-elective hospital events [rehabilitation, physician, incurred but not reported (IBNR)](12 months)
  • Determine the impact of multidisciplinary team interventions versus usual care on total outpatient costs (physician, pharmacy,rehabilitation)(12 months)
  • Determine the impact of multidisciplinary team interventions versus usual care on satisfaction with care(12 months)
  • Determine the impact of multidisciplinary team interventions versus usual care on rate of non-elective hospitalizations by chronic condition(12 months)
  • Determine the impact of multidisciplinary team interventions versus usual care on non-elective hospital readmissions at 30, 60, and 90 days following the first non-elective hospitalization event(12)
  • Determine the impact of multidisciplinary team interventions versus usual care on the length of stay (LOS) of each non-elective hospitalization(12 months)

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