New York, NYNCT07116629Now EnrollingIRB Ready

Health-Related Social Needs Clinical Trial in New York, NY

Access cutting-edge health-related social needs treatment through this clinical trial at a research site in New York. Study-provided care at no cost to qualified participants.

Sponsored by NYU Langone Health

Quick Self-Assessment

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Preparing your pre-screening questions…

Expert Care in New York

Access health-related social needs specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related health-related social needs treatment provided free

Apply for This New York Location

Check if you qualify for this health-related social needs clinical trial in New York, NY

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to New York

    Convenient for NY residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit New York site if eligible
  4. 4Begin participation

About This Health-Related Social Needs Study in New York

This study evaluates a proposed community-based implementation strategy to scale up screening, identification, and intervention on Health-Related Social Needs (HRSN) among persons on Long-Acting Injectable Pre-exposure Prophylaxis (LAI-PrEP). To do so, (1) screening for HRSN will occur at provider visits every 4 months, (2) navigation and establishment of connections with community resources through collaboration with two established community-based organization (CBO) partners, and (3) development of a tracking system integrated into the Electronic Medical Record (EMR) for monitoring and assessment of referral outcomes.

Sponsor: NYU Langone Health

Who Can Participate

Inclusion Criteria

For Patient participant group: In order to be eligible for participation in this study, an individual must meet all of the following criteria:
18 years of age or older
Does not have HIV AND vulnerable for HIV infection per WHO, NHS, and CDC recommendations
On or initiating LAI-PrEP as part of standard of care prior to study participation
Identify as either a Black/Latine cisgender woman OR Black/Latine MSM OR Transgender or Nonbinary Individual
Capacity and willingness to provide consent For Medical Staff participant group: In order to be eligible for participation in this study, an individual must meet all of the following criteria:
18 years of age or older
Works with patients who go to the Bellevue Pride Center
Be employed at NYU Langone Health or NYC H+H/Bellevue as one of the following occupations
Clinical Pharmacist
Medical Phlebotomist
Social Worker/Navigator
Community Health Worker
Medical Leader (i.e., director of services) For CBO Partner participant group: In order to be eligible for participation in this study, an individual must meet all of the following criteria:
18 years of age or older
Works with patients who go to the Bellevue Pride Center
Be employed at one of the established CBOs
Capacity and willingness to provide consent For Patient Who Declines LAI-PrEP participant group: In order to be eligible for participation in this study, an individual must meet all of the following criteria:
18 years of age or older
Declines LAI-PrEP as part of standard of care
Capacity and willingness to provide consent

Exclusion Criteria

For Patient participant group: An individual who meets any of the following criteria will be excluded from participation in this study:
Less than 18 years old
Known HIV seropositive status or test positive at screening
Does not identify as one of the listed priority populations
Not fluent in either English or Spanish
Not interested in HIV PrEP
Not willing to consent for study participation
Does not reside within New York State
Pregnant or planning to become pregnant at the time of consent.
Without capacity to consent to participate in the study For Medical Staff participant group: An individual who meets any of the following criteria will be excluded from participation in this study:
Do not work with patients who go to the Bellevue Pride Center
Is not employed at NYU Langone Health or NYC/H+H Bellevue as one of the following occupations
Clinical Pharmacist
Medical Phlebotomist
Social Worker
Community Health Worker
Medical Leader (i.e., directors of services) For CBO Partner participant group: An individual who meets any of the following criteria will be excluded from participation in this study: • Does not work with patients who go to the Bellevue Pride Center For Patient Who Declines LAI-PrEP participant group: An individual who meets any of the following criteria will be excluded from participation in this study:
Less than 18 years old
Interested in initiating LAI-PrEP as part of standard of care or on LAI-PrEP

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in New York?

Yes, this clinical trial (NCT07116629) has an active research site in New York, NY that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Health-Related Social Needs Treatment Options in New York, NY

If you're searching for health-related social needs treatment options in New York, NY, this clinical trial (NCT07116629) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our New York research site is actively enrolling participants for this clinical trial. You'll receive care from experienced health-related social needs specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all health-related social needs clinical trials near you to find additional studies recruiting in your area.

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