Wisconsin Evaluation of Emergency Department Care Coordination

January 8, 2025 updated by: University of Wisconsin, Madison

Evaluation of an Intensive Care Coordination Program to Reduce Use of Hospital Emergency Department Services by Wisconsin Medicaid Members

The State of Wisconsin is now expanding its investment in care coordination models as an effort to reduce inappropriate hospital emergency department (ED) use, improve health outcomes, and reduce Medicaid expenditures. This effort begins with a pilot program to support emergency department care coordination in hospitals and health systems that apply and are selected to participate in the pilot program.

The Wisconsin Medicaid program seeks to understand whether this program achieves its intended goals and, specifically, whether the Medicaid payment for such care coordination services produces the intended program outcomes. Hospitals will select members that will receive care coordination services. In a quasi-experimental approach, the study team will compare members that do vs. do not receive the services will be used examine the effects of care coordination and referrals on total ED visits, primary-care treatable ED visits, non-emergent ED visits, and health care costs, as well as the specific effects of referring patients to providers who offer low-cost and after-hours care. To assess the importance of targeting, study team will conduct stratified analyses of vulnerable groups such as people with disabilities and individuals with specific clinical needs.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

3405

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Wisconsin
      • Appleton, Wisconsin, United States, 54911
        • ThedaCare
      • Glendale, Wisconsin, United States, 53217
        • Ascension Wisconsin
      • Milwaukee, Wisconsin, United States, 53202
        • Aurora Health Care
      • Wauwatosa, Wisconsin, United States, 53226
        • Froedtert Health , Wisconsin

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 64 years (Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Inclusion Criteria:

  • Adults who are Medicaid enrolled
  • Have had 5+ emergency department visits in the past year

Exclusion Criteria:

  • Participants who are concurrently eligible for Medicare
  • Children (individuals age <18 years).

Description

Inclusion Criteria:

  • Adults who are Medicaid enrolled
  • Have had 5+ emergency department visits in the past year

Exclusion Criteria:

  • Participants who are concurrently eligible for Medicare
  • Children (individuals age <18 years).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Intensive Care Coordination
Intensive Care Coordination along with Standard of Care

Intensive care coordination will include:

  • Discharge instructions and contacts for following up on care and treatment
  • Referral information
  • Appointment scheduling
  • Medication instructions
  • Intensive care coordination by a social worker, case manager, nurse, or care coordinator to connect Medical Assistance (MA) recipient to a primary care provider or to a managed care organization
  • Information about other health and social resources, such as transportation and housing
  • Sharing of information (discharge instructions, medication information, and care plan information) with managed care organization in which patients are enrolled, if applicable
Control
Standard of Care alone

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Total Number of Emergency Department Visits
Time Frame: 6 months
6 months
Total Number of Emergency Department Visits
Time Frame: 12 months
12 months
Total Number of Emergency Department Visits
Time Frame: 18 months
18 months
Total Number of Emergency Department Visits
Time Frame: 24 months
24 months
Total Number of Emergency Department Visits for Primary Care Preventable and/or Non-Emergent Conditions
Time Frame: 6 months
6 months
Total Number of Emergency Department Visits for Primary Care Preventable and/or Non-Emergent Conditions
Time Frame: 12 months
12 months
Total Number of Emergency Department Visits for Primary Care Preventable and/or Non-Emergent Conditions
Time Frame: 18 months
18 months
Total Number of Emergency Department Visits for Primary Care Preventable and/or Non-Emergent Conditions
Time Frame: 24 months
24 months
Cost to Medicaid for all Emergency Department Visits
Time Frame: 6 months
6 months
Cost to Medicaid for all Emergency Department Visits
Time Frame: 12 months
12 months
Cost to Medicaid for all Emergency Department Visits
Time Frame: 18 months
18 months
Cost to Medicaid for all Emergency Department Visits
Time Frame: 24 months
24 months
Cost to Medicaid for Emergency Department Use for Primary Care Preventable and/or Non-Emergent Conditions
Time Frame: 6 months
6 months
Cost to Medicaid for Emergency Department Use for Primary Care Preventable and/or Non-Emergent Conditions
Time Frame: 12 months
12 months
Cost to Medicaid for Emergency Department Use for Primary Care Preventable and/or Non-Emergent Conditions
Time Frame: 18 months
18 months
Cost to Medicaid for Emergency Department Use for Primary Care Preventable and/or Non-Emergent Conditions
Time Frame: 24 months
24 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total Number of Primary Care Visits
Time Frame: 6, 12, 18, and 24 months
6, 12, 18, and 24 months
Number of Participants Who Used Any Primary Care Visits
Time Frame: 6, 12, 18, and 24 months
6, 12, 18, and 24 months
Number of Participants Who Used Specialty Care Visits
Time Frame: 6, 12, 18, and 24 months
6, 12, 18, and 24 months
Total Number of Specialty Care Visits
Time Frame: 6, 12, 18, and 24 months
6, 12, 18, and 24 months
Number of Participants with Any Hospitalizations
Time Frame: 6, 12, 18, and 24 months
6, 12, 18, and 24 months
Number of Hospitalization Events
Time Frame: 6, 12, 18, and 24 months
6, 12, 18, and 24 months
Number of visits to use behavioral health resources, if applicable for the participant
Time Frame: 6, 12, 18, and 24 months
6, 12, 18, and 24 months
Number of visits to use alcohol and other drug abuse resources if applicable for the participant
Time Frame: 6, 12, 18, and 24 months
6, 12, 18, and 24 months
Total Cost Related to the Use of Behavioral Health Resources if applicable for the participant
Time Frame: 6, 12, 18, and 24 months
6, 12, 18, and 24 months
Total Cost Related to Use of Alcohol and other Drug Abuse Resources if applicable for the participant
Time Frame: 6, 12, 18, and 24 months
6, 12, 18, and 24 months
Total costs of care to Medicaid
Time Frame: 6, 12, 18, and 24 months
6, 12, 18, and 24 months
Number of participants enrolled in Temporary Assistance for Needy Families (TANF)
Time Frame: 6, 12, 18, and 24 months
6, 12, 18, and 24 months
Number of participants enrolled in FoodShare
Time Frame: 6, 12, 18, and 24 months
FoodShare is a program that helps people with limited resources buy the food they need for good health.
6, 12, 18, and 24 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Rebecca Myerson, MPH, PhD, University of Wisconsin, Madison

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2022

Primary Completion (Actual)

December 15, 2024

Study Completion (Actual)

December 15, 2024

Study Registration Dates

First Submitted

September 9, 2020

First Submitted That Met QC Criteria

September 14, 2020

First Posted (Actual)

September 16, 2020

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 8, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2020-1211
  • A538500 (Other Identifier: UW- Madison)
  • SMPH/POP HEALTH SCI/POP HEALTH (Other Identifier: UW Madison)
  • MSN240705 (Other Grant/Funding Number: DHHS, CENTERS FOR MEDICARE & MEDICAID SE)
  • Protocol Version April 2020 (Other Identifier: UW Madison)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Emergency Department Visit

Clinical Trials on Intensive Care Coordination

Subscribe