- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06342375
Enrollment Barriers, Procedural Denials, and Loss of Medicaid Coverage
April 7, 2026 updated by: University of Wisconsin, Madison
The goal of this study is to try new outreach methods to improve access to Medicaid for those who lost Medicaid for procedural reasons. The main questions it aims to answer are:
- How does a live phone call from a Navigator impact Medicaid enrollment among people who lost Medicaid coverage for procedural reasons?
- What is the effectiveness of outreach using a live call rather than a pre-recorded call?
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
230000
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Rebecca Myerson, PhD
- Phone Number: 608-263-2082
- Email: rmyerson@wisc.edu
Study Locations
-
-
Wisconsin
-
Madison, Wisconsin, United States, 53705
- Recruiting
- University of Wisconsin - Madison
-
Contact:
- Rebecca Myerson, PhD
- Phone Number: 608-263-2082
- Email: rmyerson@wisc.edu
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Eligible for Medicaid
- Lost Medicaid coverage between June 2024 and November 2025
Exclusion Criteria:
- Preferring a language other than English, Spanish, or Hmong
- No working phone number
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
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Live Outreach
People in this cohort will receive a live outbound call from a Navigator
|
Participants will receive either a live or pre-recorded outbound phone call
|
|
Experimental: Pre-recorded Outreach
People in this cohort will receive a pre-recorded outbound call providing a hotline number
|
Participants will receive either a live or pre-recorded outbound phone call
|
|
No Intervention: No outreach
People in this cohort will not receive outreach of any kind
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of people who successfully renew their Medicaid coverage within 3 months of receiving the live outbound call
Time Frame: 3 months
|
Numbers will be counted using Wisconsin administrative data on Medicaid enrollment housed at the UW Institute for Research on Poverty.
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Duration of coverage gaps
Time Frame: 6 months
|
Duration of gaps will be measured using Wisconsin administrative data on Medicaid enrollment housed at the UW Institute for Research on Poverty.
|
6 months
|
|
Number of people who successfully renew their Medicaid coverage within 6 months of receiving the live outbound call
Time Frame: 6 months
|
Numbers will be counted using Wisconsin administrative data on Medicaid enrollment housed at the UW Institute for Research on Poverty.
|
6 months
|
|
Number of people who successfully renew their Medicaid coverage within 6 months of receiving the pre-recorded outbound call
Time Frame: 6 months
|
Numbers will be counted using Wisconsin administrative data on Medicaid enrollment housed at the UW Institute for Research on Poverty.
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Rebecca Myerson, 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)
February 12, 2025
Primary Completion (Estimated)
February 1, 2027
Study Completion (Estimated)
December 1, 2027
Study Registration Dates
First Submitted
March 26, 2024
First Submitted That Met QC Criteria
April 1, 2024
First Posted (Actual)
April 2, 2024
Study Record Updates
Last Update Posted (Actual)
April 8, 2026
Last Update Submitted That Met QC Criteria
April 7, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2024-0434
- A538500 (Other Identifier: UW- Madison)
- SMPH/POP HEALTH SCI/POP HLTH (Other Identifier: UW- Madison)
- Protocol Version 4/17/2025 (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.
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