A Seek, Test, and Treat Intervention to Reduce Chlamydia Trachomatis Disparities
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Chlamydia, gonorrhea, syphilis, and HIV screening.
- Who it may be relevant to
- Registry conditions: Chlamydia, Gonorrhea, Hiv, Syphilis. Basic parameters: 15 years — 26 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
A Seek, Test, and Treat Intervention to Reduce Chlamydia Trachomatis Disparities in Black Youth Living in the Deep South
Overview
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.
Interventions
- 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.
Primary outcome measures
- Rate of chlamydia in women [Time frame: up to 60 months]
Secondary outcome measures (1)
- Rate of gonorrhea in women [Time frame: up to 60 months]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Screening
Study locations
United States · 1 center
- Tulane University Celia Scott Weatherhead School of Public Health and Tropical Medicine — New Orleans
Identifiers
NCT: NCT06428643 · 2024-377