Status:
COMPLETED
Zenyth: Motivational Interviewing-based Telehealth Intervention for Bacterial Sexually Transmitted Infection Screening
Lead Sponsor:
University of Michigan
Collaborating Sponsors:
National Institutes of Health (NIH)
National Institute of Allergy and Infectious Diseases (NIAID)
Conditions:
Sexually Transmitted Diseases
Gonorrhea
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
In the United States (US), gay and bisexual men living with human immunodeficiency virus (HIV) bear a heavy burden of bacterial sexually transmitted infections (STIs) such as gonorrhea, chlamydia, and...
Detailed Description
Participants will be recruited from across the US via social media advertising and peer referral. Seventy-five participants that complete an online survey (called the baseline survey) will be asked to...
Eligibility Criteria
Inclusion
- Individual self-reports identifying as a man (regardless of sex assigned at birth) in the eligibility screener
- Individual self-reports residing in a US state or territory in the eligibility screener
- Individual self-reports being physically located in a US state or territory when completing study activities in the eligibility screener
- Individual self-reports being greater than or equal to (≥)18 years of age in the eligibility screener
- Individual self-reports being of legal age to provide consent for research participation in the US state or territory of residence in the eligibility screener
- Individual self-reports having been diagnosed with HIV in the eligibility screener
- Individual self-reports having any kind of condomless sex (e.g., oral, anal) with ≥2 men in the past year in the eligibility screener
- Individual self-reports being willing to provide contact information (full name, email address, mobile phone number, and mailing address) in the eligibility screener
- Individual self-reports being able to participate in live AV conferencing sessions using an internet-connected device (e.g., computer, tablet, smartphone) in the eligibility screener
- Individual self-reports being willing to receive a box that contains kits to self-collect a urine sample, a throat swab, a rectal swab, and a blood sample for bacterial STI testing in the eligibility screener
- Individual provides valid contact information (full name, email address, mobile phone number, and mailing address) in the contact information form
- Individual completes the baseline survey in order to receive the intervention
Exclusion
- Individual self-reports not identifying as a man (regardless of sex assigned at birth) in the eligibility screener
- Individual self-reports not residing in a US state or territory in the eligibility screener
- Individual self-reports not being physically located in a US state or territory when completing study activities in the eligibility screener
- Individual self-reports not being ≥18 years of age in the eligibility screener
- Individual self-reports not being of legal age to provide consent for research participation in the US state or territory of residence in the eligibility screener
- Individual self-reports not having been diagnosed with HIV in the eligibility screener
- Individual self-reports not having any kind of condomless sex (e.g., oral, anal) with ≥2 men in the past year in the eligibility screener
- Individual self-reports not being willing to provide contact information (full name, email address, mobile phone number, and mailing address) in the eligibility screener
- Individual self-reports not being able to participate in live AV conferencing sessions using an internet-connected device (e.g., computer, tablet, smartphone) in the eligibility screener
- Individual self-reports not being willing to receive a box that contains kits to self-collect a urine sample, a throat swab, a rectal swab, and a blood sample for bacterial STI testing in the eligibility screener
- Individual does not provide valid contact information (full name, email address, mobile phone number, and mailing address) in the contact information form
- Individual does not complete the baseline survey in order to receive the intervention
Key Trial Info
Start Date :
April 19 2024
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 7 2025
Estimated Enrollment :
75 Patients enrolled
Trial Details
Trial ID
NCT06100250
Start Date
April 19 2024
End Date
March 7 2025
Last Update
July 1 2025
Active Locations (1)
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1
University of Michigan
Ann Arbor, Michigan, United States, 48109