Actively Recruiting
Addressing Durable Health Disparities Through Critical Time Legal Interventions in Medically Underserved Latinx and Migrant Communities
Led by Stony Brook University · Updated on 2025-02-12
1140
Participants Needed
1
Research Sites
130 weeks
Total Duration
On this page
Sponsors
S
Stony Brook University
Lead Sponsor
U
University of Central Florida
Collaborating Sponsor
AI-Summary
What this Trial Is About
This clinical trial will examine the effects of legal services on primary care outcomes for medically underserved communities. The aims of the study are: 1. To test the effectiveness and cost-benefits of a critical-time intervention Medical-Legal Partnership (CTI-MLP) on patient outcomes. 2. To determine the most efficient mechanisms for CTI-MLP delivery. 3. To develop innovative community engagement strategies for addressing health-harming legal needs within community health centers. Eligible patients will be asked to complete a questionnaire 4 times, first when they join the study and then at 3 months, 6 months, and 12 months. In the survey, they will be asked to provide information about themselves, their health care, aspects of their daily life, and hardships they face. They will also allow researchers to access their electronic health record information housed in the community-based organization and attorney notes. Patient information will be completely confidential and de-identified, meaning, the research team will not know the identity of the person who answered the questions. Participating community health centers will be randomized (assigned by chance) to provide basic legal information and referral to legal aid; or have an attorney on-site to provide legal aid to those who screen for legal needs.
CONDITIONS
Official Title
Addressing Durable Health Disparities Through Critical Time Legal Interventions in Medically Underserved Latinx and Migrant Communities
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 13 years or older
- Impacted by urgent health-harming legal needs or risks as confirmed by screening
- Willing and able to consent to participate and allow access to electronic health records
- Does not intend to relocate within 12 months of enrollment
You will not qualify if you...
- Does not meet all inclusion criteria
- Self-reports being sentenced to serve under state or federal custody with sentence starting within 12 months after enrollment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Betances Health Center
New York, New York, United States, 10002
Actively Recruiting
Research Team
M
Miguel A Munoz-Laboy, DrPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here