NCT07446764Not yet recruiting
Integrated Health Services (IHS): A Structural Intervention to Improve HIV/STI Screening and PrEP Navigation in Primary Care
Source: ClinicalTrials.gov · Last updated 3 Mar 2026
Brief summary (registry, in English)
The goal of this clinical trial is to learn whether integrating routine, opt-out HIV and STI testing and pre-exposure prophylaxis (PrEP) navigation into primary care increases use of these services among adults ages 18 to 45 receiving care at Federally Qualified Health Centers in Mississippi. The main questions it aims to answer are: 1. Does the integrated model increase HIV and STI testing compared with standard care? 2. Does the integrated model increase PrEP navigation activity for eligible patients? 3. How do patients and clinic staff experience the integrated model in terms of satisfaction, comfort discussing sexual health, and feasibility in daily workflows? Researchers will compare a standard-care period to a period when the integrated model is in place to see if the integrated model improves service use and patient experience. Participants will: 1. Receive usual primary care, with HIV/STI testing and PrEP discussions offered as a routine, opt-out part of care during the integrated period 2. Be invited, if eligible, to complete a brief survey about their clinic experience 3. For staff, be invited to take part in a short survey or interview about clinic workflows and the integrated model
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 700 (estimated)
- First submitted
- 10 Feb 2026
- Start date
- Feb 2027
- Primary completion date
- Apr 2028
- Lead sponsor
- My Brother's Keeper, Inc.
- Diseases
- HIV
- NCT number
- NCT07446764
What you commit to
- Study type: Interventional
- Planned participants: 700
- From Feb 2027 to the primary completion date, Apr 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Age
- Younger than 18 years or older than 45 years.
Other
- Critically ill, psychiatrically unstable, or lacking capacity to provide informed consent for research participation.
- Unable to understand English for consent and survey/interview procedures.
- For staff key informants: unable or unwilling to provide informed consent for interviews or surveys.
Who the study is looking for
- Adults ages 18 to 45 years.
- Receiving primary care services at participating Federally Qualified Health Center (FQHC) clinics in Canton or Yazoo City, Mississippi.
- Able to understand and read English (for participation in surveys and interviews).
- For staff key informants: current clinical, administrative, or support role at a participating FQHC site with responsibilities related to primary care, HIV/STI services, or care coordination.
Age in the registry: 18 years to 45 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| My Brother's Keeper, Inc. Coordinator of this site? Confirm its status | Ridgeland | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.