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

NCT ID: NCT06428643

Last Updated: 2024-05-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

2322 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-09-01

Study Completion Date

2029-09-01

Brief Summary

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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

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Conditions

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Chlamydia Gonorrhea Hiv Syphilis

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Community based screening of young men for chlamydia, gonorrhea, HIV, and syphilis. Expedited treatment for positive subjects and their sexual partners.
Primary Study Purpose

SCREENING

Blinding Strategy

NONE

None (Open Label)

Study Groups

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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.

Group Type EXPERIMENTAL

Chlamydia, gonorrhea, syphilis, and HIV screening

Intervention Type OTHER

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.

Interventions

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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.

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

15 Years

Maximum Eligible Age

26 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institutes of Health (NIH)

NIH

Sponsor Role collaborator

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

Sponsor Role collaborator

Tulane University

OTHER

Sponsor Role lead

Responsible Party

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Patricia Kissinger

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Patricia Kissinger, PhD

Role: CONTACT

504-988-7320

Other Identifiers

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2024-377

Identifier Type: -

Identifier Source: org_study_id

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