An interventional study of Chlamydia, gonorrhea, syphilis, and HIV screening in Chlamydia, Gonorrhea and Hiv, sponsored by Tulane University. Recruiting at 1 site in United States. Open to participants aged 15 Years to 26 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-21.
Sponsored by Tulane University · Not applicable, Interventional, and Screening
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.
Exclusion Criteria:
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.
Other: Chlamydia, gonorrhea, syphilis, and HIV screening
Individuals aged 15-26 years old will be tested for chlamydia, gonorrhea, HIV, and syphilis at community based venues. Individuals who test positive for chlamydia and gonorrhea and their sexual partners will be offered expedited treatment at participating pharmacies. Individuals who test positive will be asked to be rescreened for Ct/GC at 3 months post treatment.
Rate of chlamydia in women
Primary outcome
Time frame: up to 60 months
Index participant medication pickup rate
Percentage of index participants who obtain their prescribed medication from a partnering pharmacy among all index participants who report intending to pick up the medication. Medication receipt will be determined from pharmacy billing records. Rates will be calculated monthly.
Time frame: up to 60 months
Partner medication pickup rate
Percentage of partners who obtain their prescribed medication from a partnering pharmacy among all partners reported as intending to pick up the medication. Medication receipt will be determined from pharmacy billing records. Rates will be calculated monthly.
Time frame: 60 months
Self reported treatment of index participants and partners
Number and percentage of index participants who report that they and all applicable partner(s) received treatment. The denominator will include index participants who provide follow-up information about their own and their partner(s)' treatment status.
Time frame: 60 months
Plan to share: Yes — We will provide de-identified data to persons who submit a reasonable request with appropriate institutional approval after the primary and secondary request questions have been published.
Supporting information: Sap, Icf
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Tulane University