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NCT06428643 Clinical Trial

A Seek, Test, and Treat Intervention to Reduce Chlamydia Trachomatis Disparities

Hiv Clinical Trial

Official title:
A Seek, Test, and Treat Intervention to Reduce Chlamydia Trachomatis Disparities in Black Youth Living in the Deep South

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06428643
Other study ID # 2024-377
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 1, 2024
Est. completion date September 1, 2029

Study information
Verified date May 2024
Source Tulane University
Contact Patricia Kissinger, PhD
Phone 504-988-7320
Email kissing@tulane.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 2322
Est. completion date September 1, 2029
Est. primary completion date September 1, 2028
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 15 Years to 26 Years
Eligibility 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

Related Conditions & MeSH terms

Intervention

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.

Locations
Country Name City State
n/a

Sponsors (3)
Lead Sponsor Collaborator
Tulane University National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH)

Outcome
Type Measure Description Time frame Safety issue
Primary Rate of chlamydia in women Primary outcome up to 60 months
Secondary Rate of gonorrhea in women Secondary outcome up to 60 months
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