- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07594782
ED Medicaid Support
May 11, 2026 updated by: Hackensack Meridian Health
Maintaining Continuous Medicaid Coverage for Eligible Children in New Jersey
The study introduces a bedside intervention assisting families with the enrollment or re-enrollment process through patient direct contact with NJFamily Care and financial departments, using an emergency department (ED)-based navigator tool.
The primary objective is to identify the barriers contributing to the lack of insurance coverage through NJ Family Care coverage using a brief survey with the parents of children who are treated in the ED and identified as uninsured, and to study the effect of a bedside intervention designed to assist families with the enrollment or re-enrollment process.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
180
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: Daisy Negron, MBA, BSN, RN
- Phone Number: 551-996-3206
- Email: Daisy.Negron@hmhn.org
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
Yes
Description
Inclusion Criteria:
- Parent/guardian/ legal authorized representative (age 18 years or older) with children aged: 1 month to 17 years of age who obtain care in the pediatric emergency department
- Child Uninsured (ie, Charity Care, HUMC Charity Care, Pending Medicaid, Self-Pay)
- Interested in applying or receiving assistance with NJfamilycare
- Not pending private insurance coverage
- Primary language of the parent or guardian is identified as English
- Pediatric patient lives in New Jersey
Exclusion Criteria:
- Parent/guardian/legal authorized representative with children aged: less than 1 month and greater than 17 years old Insured pediatric patient Parent/ Guardian/Legal Authorized Representative not present Parent/ Guardian/Legal Authorized Representative age 17 years or younger Primary language not identified as English Patients visiting the Emergency Department related to Motor Vehicle Accidents Already participated in this study
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: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Bedside intervention and support
A bedside intervention assisting families with the enrollment or re-enrollment process through patient direct contact with NJFamily Care and local financial departments, using an ED-based navigator tool.
|
Navigation through financial systems and linkage to resources to connect families and ultimately help them gain access to insurance for the pediatric patient.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Barriers to medicaid enrollment or reenrollment
Time Frame: Survey is completed upon enrollment
|
Outcome of questionnaire regarding barriers expressed as percentage of participants who identified each barrier
|
Survey is completed upon enrollment
|
|
Rate of Successful Medicaid Enrollment or Re-enrollment Approval
Time Frame: Assessed via participant follow-up call or review of the electronic health record at 90 days post-intervention.
|
The proportion of the enrolled participants who reported approval for Medicaid coverage.
This outcome measures the ultimate success of the intervention of re-establishing health insurance.
|
Assessed via participant follow-up call or review of the electronic health record at 90 days post-intervention.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Enrollment in Temporary Insurance Coverage
Time Frame: Assessed via participant follow-up within 10 days (+/- 5 days) post-intervention and/or chart review.
|
The proportion of participants who, after receiving additional assistance, were successfully enrolled in a temporary or bridge insurance plan, known as presumptive eligibility.
This measures the intervention's success in providing a safety net for families during the Medicaid application waiting period.
|
Assessed via participant follow-up within 10 days (+/- 5 days) post-intervention and/or chart review.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Karen Eigen, MD, MPH, Hackensack Meridian Health
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 (Estimated)
May 15, 2026
Primary Completion (Estimated)
May 15, 2028
Study Completion (Estimated)
May 15, 2028
Study Registration Dates
First Submitted
May 11, 2026
First Submitted That Met QC Criteria
May 11, 2026
First Posted (Actual)
May 19, 2026
Study Record Updates
Last Update Posted (Actual)
May 19, 2026
Last Update Submitted That Met QC Criteria
May 11, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Pro2026-0127
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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