A Seek, Test, and Treat Intervention to Reduce Chlamydia Trachomatis Disparities
Not Applicable
Not yet recruiting
- Conditions
- ChlamydiaGonorrheaHivSyphilis
- Interventions
- Other: Chlamydia, gonorrhea, syphilis, and HIV screening
- Registration Number
- NCT06428643
- Lead Sponsor
- Tulane University
- Brief Summary
This study includes testing for four STIs (chlamydia, gonorrhea, syphilis, and HIV) at no cost. If positive, individual subjects will also be counseled and offered options for treatment for themselves and their sex partners that may include no cost expedited treatment and the option to be rescreened 3 months after treatment.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 2322
Inclusion Criteria
- Identifies as African American or Black
- 15-26 years of age
- Lives or spends most of their time in Orleans Parish
- Had vaginal sex at least once
Exclusion Criteria
- Unwilling or unable to provide informed consent
- Unable to speak or understand English
- Previously enrolled in the study
- Known to be pregnant
- Known HIV positive status
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Chlamydia, gonorrhea, syphilis, and HIV screening Chlamydia, gonorrhea, syphilis, and HIV screening Community screening of individuals for chlamydia and gonorrhea is not normally done. We are testing to see if this intervention will impact the rates of chlamydia among women.
- Primary Outcome Measures
Name Time Method Rate of chlamydia in women up to 60 months Primary outcome
- Secondary Outcome Measures
Name Time Method Rate of gonorrhea in women up to 60 months Secondary outcome