- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02841930
ActionHealthNYC Research Study
ActionHealthNYC: A Health Care Access Program for the Uninsured
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The ActionHealthNYC program is a year-long demonstration program to improve access to high quality health care for NYC resident immigrants who do not qualify for public insurance with incomes at or below 200% of the Federal Poverty Level (FPL). Our goal in piloting the program and conducting the research study is to understand the following questions:
- For clients participating in the ActionHealthNYC program, do they report having easier access to health care?
- What are the differences in health care utilization for participants in the ActionHealthNYC program and those not in the program?
- Do the participants in the ActionHealthNYC program report fewer barriers to needed care when compared to those not in the program?
- Are the participants in the ActionHealthNYC program more likely to have received preventive services according to the United States Preventive Services Task Force (USPTF) or recommended services for those with a qualifying condition through their medical home?
- How does the likelihood of receiving a new diagnosis compare between the ActionHealthNYC member group and the study group?
- How does emergency department and hospital use compare between the ActionHealthNYC member group and the study group?
We will be conducting a randomized controlled trial (RCT) where we will be enrolling 2,400 people that meet the eligibility criteria and randomizing half into the ActionHealth NYC program. We will be employing a mixed methods approach to address differences between participants randomized to receive enhanced services through ActionHealthNYC (AHNYC) and those receiving usual care, utilizing surveys, secondary data analysis, key informant interviews and participant focus groups.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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New York
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Long Island City, New York, United States, 11101
- New York City Department of Health and Mental Hygiene
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- New York City residents who are uninsured, 19 and older and
- Not currently eligible for Medicaid, Essential Plan, or
- Not currently eligible for private insurance via federal insurance marketplace subsidies due to their immigration status.
Exclusion Criteria:
- Not a New York City resident
- Currently eligible for Medicaid, Essential Plan or private insurance at state exchange with federal subsidies
- Income above 200% of the federal poverty level (FPL)
Enrollees are required to have the NYC Municipal identification card (IDNYC). If they do not have the card, however, they can obtain it and come back for enrollment.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Member
The member group will be able to join ActionHealth NYC program, where they are assigned a primary care physician and have a standardized fee scale for services obtained in network.
Laboratory, diagnostic, and specialty services can be obtained at network H+H locations.
They will be offered recommended USPSTF A+B tests/screenings, HIV and TB screening (if indicated), and care coordination.
If they are deemed "high risk," enhanced care coordination services will be offered.
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care coordination, covered preventive services, and standardized costs for ambulatory care
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No Intervention: Study
The study group will be counseled on their options to access health care, including at public hospitals and community health centers.
They will receive no additional services from the study.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Improved access to healthcare
Time Frame: One year
|
e.g.
fewer delays in getting needed care
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One year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Enhanced healthcare utilization
Time Frame: One year
|
e.g.
emergency department care utilization rate
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One year
|
Reduced barriers to needed care
Time Frame: One year
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e.g. financial barriers
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One year
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Enhanced utilization of preventive services
Time Frame: One year
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Utilization of USPSTF recommended services through primary care home
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One year
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Increased number of new diagnoses
Time Frame: One year
|
One year
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Rishi Sood, MPH, New York City Department of Health and Mental Hygiene
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- NYCDOHMH IRB 16-020
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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