- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06454019
Phone Outreach Nudges Among Individuals Losing Medicaid Coverage
June 10, 2024 updated by: Marina Lovchikova, Covered California
Evaluating Impact of Outreach Nudges Among Individuals Losing Medicaid Coverage in California
In May 2023, Covered California, California's ACA marketplace, implemented its automatic enrollment program for individuals losing Medicaid coverage, as defined by Senate Bill 260.
If individuals are found eligible for subsidized marketplace coverage, individuals will be automatically enrolled in the lowest cost silver plan available to them, but individuals must still take action to confirm their plan or pay their first month's premium.
To identify whether the phone outreach is the effective outreach strategy to increase take-up in this population, Covered California implemented this intervention.
The results of this evaluation will inform operational and budgeting decisions.
Study Overview
Status
Enrolling by invitation
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
60045
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 Locations
-
-
California
-
Sacramento, California, United States, 95835
- Covered California
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Lost Medi-Cal (California's Medicaid coverage) in July 2023-June 2024
- Auto-enrolled into lowest cost silver plan with Covered California as per Senate Bill 260 and have not opted-in (effectuated) into the coverage
- Have a valid phone number on the health insurance application
- Do not have a delegated agent to their case
- Still have Covered California Program eligibility, not reverted back to Medi-Cal coverage
- Have English or Spanish as preferred speaking language
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Control Group without a phone call
Control Group was assigned to receive no phone outreach
|
Standard notification letter without phone outreach to individuals losing Medicaid and auto-enrolled into Covered California plan to nudge them to act
|
|
Experimental: Treatment Group with a phone call
Treatment group was assigned to receive a phone call from Covered California call center
|
Phone outreach to individuals losing Medicaid and auto-enrolled into Covered California plan to nudge them to act
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Health Plan Effectuation
Time Frame: within 30 days from the start date of plan they are auto-enrolled into
|
A binary indicator for whether a consumer is effectuated into (paid for, opt-in into) Covered California plan, either the plan assigned through the auto-enrollment process, or into another plan chosen by the consumer by the end of the month at which outreach was conducted
|
within 30 days from the start date of plan they are auto-enrolled into
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Tenure with Covered California (measured in months)
Time Frame: measured 1-2 years after the intervention
|
A length of tenure with Covered California plan within calendar year and/or beyond
|
measured 1-2 years after the intervention
|
|
Office visit
Time Frame: measured 1-2 years after the intervention
|
A binary indicator for whether someone had an office visit during 1-2 years since the intervention
|
measured 1-2 years after the intervention
|
|
Prescriptions filled
Time Frame: measured 1-2 years after the intervention
|
A binary indicator for whether someone had a prescription drug fill during 1-2 years since the intervention
|
measured 1-2 years after the intervention
|
|
Emergency Room Visit
Time Frame: measured 1-2 years after the intervention
|
A binary indicator for whether someone had an emergency room visit during 1-2 years since the intervention
|
measured 1-2 years after the intervention
|
|
Hospital admission
Time Frame: 1-2 years before and after the intervention
|
A binary indicator for whether someone had a hospital admission 1-2 years before and 1-2 years after the intervention
|
1-2 years before and after the intervention
|
|
Out-of-pocket spending on healthcare services
Time Frame: measured 1-2 years after the intervention
|
Total out-of-pocket spending for the 1-2 years since the intervention
|
measured 1-2 years after the intervention
|
|
Uninsured
Time Frame: measured 1-2 years after the intervention
|
A binary indicator for whether someone self-reported being uninsured while filing their taxes
|
measured 1-2 years after the intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Emory Wolf, MPP, Covered California
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)
August 1, 2023
Primary Completion (Estimated)
September 1, 2024
Study Completion (Estimated)
November 1, 2024
Study Registration Dates
First Submitted
June 5, 2024
First Submitted That Met QC Criteria
June 10, 2024
First Posted (Actual)
June 12, 2024
Study Record Updates
Last Update Posted (Actual)
June 12, 2024
Last Update Submitted That Met QC Criteria
June 10, 2024
Last Verified
June 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- SB260-OCC-2023
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
The researchers are committed to sharing as much data as possible for replication, consistent with the privacy and security requirements of the state agency that govern the re-disclosure of the data.
IPD Sharing Time Frame
Data will be available with investigator support upon publication
IPD Sharing Access Criteria
Replication data can be accessed via request to the primary investigator upon publication.
IPD Sharing Supporting Information Type
- SAP
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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