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| ID | Type | Description | Link |
|---|---|---|---|
| PR15-SFDPH-026 | Other Grant/Funding Number | California HIV/AIDS Research Program |
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| Name | Class |
|---|---|
| San Francisco Department of Public Health | OTHER_GOV |
| University of California, San Francisco | OTHER |
| San Francisco Community Health Center | UNKNOWN |
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The Stay Study is a multi-site, open-label HIV pre-exposure prophylaxis (PrEP) demonstration project for advancing PrEP delivery in the San Francisco Bay Area Transgender Community. Approximately 188 HIV-uninfected participants will be enrolled at 4 sites in San Francisco and Fremont and will be provided Truvada to take orally once daily as PrEP.
PrEP stands for Pre-Exposure Prophylaxis, an HIV prevention method that involves HIV negative people taking antiviral drugs daily to try to help prevent HIV infection. Studies with men who have sex with men (MSM) and transgender women showed that people who took PrEP were less likely to become infected with HIV than those who did not take it.
The main purpose of this PrEP Demonstration Project is to make PrEP accessible to people in the transgender community. As part of this project, we will study whether transgender women and men are interested in taking PrEP, and, if so, for how long and how frequently they take the medication and how these relate to demographics (such as race, age, and education). We will also assess reasons for stopping PrEP and measure sexual behaviors of participants in the demonstration project.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Main | Other | Emtricitabine / Tenofovir Disoproxil Oral Tablet and PrEP support. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Emtricitabine / Tenofovir Disoproxil Oral Tablet | Drug | Open-label emtricitabine 200mg/tenofovir 300mg |
|
| Measure | Description | Time Frame |
|---|---|---|
| PrEP uptake and its correlates by gender identity, race/ethnicity, age, education, site, hormone status, and risk practices | Combined analysis of PrEP acceptance and refusal rates and sociodemographic correlates of PrEP acceptance and refusal. | Baseline |
| Patterns and correlates of PrEP adherence among transgender individuals in the Stay Study. | Combined analysis of PrEP adherence rates as measured by: Tenofovir-diphosphate (TFV-DP) levels in dried blood spots (DBS); medication possession ratio; self-reported adherence. Patterns and correlates of adherence | 12 months |
| Measure | Description | Time Frame |
|---|---|---|
| Reasons transgender people choose to initiate PrEP | Reasons for initiating PrEP | Baseline |
| Reasons transgender people choose to decline PrEP | Reasons for declining PrEP |
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Inclusion Criteria:
Self-identify as a transgender woman, transgender man, or gender non-conforming
Willing and able to provide written informed consent;
Age ≥ 18 years;
HIV-1-uninfected defined per site HIV testing algorithm performed within 7 (and up to 14) days of enrollment if PrEP naïve or within 90 days if currently on PrEP (see SSP manual)
Expressed desired to use or continue PrEP, anticipated risk, or evidence of risk for acquiring HIV-1 infection including having any cisgender male or transgender female partners in the past 12 months and not in a mutually monogamous partnership with a recently tested, HIV-negative partner AND at least one of the following;
Fluent in English or Spanish
Exclusion Criteria:
Individuals with any of the following will be excluded:
Transgender or gender non-conforming
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| Name | Affiliation | Role |
|---|---|---|
| Albert Y Liu, MD, MPH | Bridge HIV, San Francisco Department of Public Health | Principal Investigator |
| Erin Wilson, DrPH | Center for Public Health Research, San Francisco Department of Public Health | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Tri-City Health Center | Fremont | California | 94538 | United States | ||
| Bridge HIV, San Francisco Department of Public Health |
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| Tri-City Health Center |
| UNKNOWN |
| California HIV/AIDS Research Program | OTHER |
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| PrEP support | Behavioral | HIV/STI testing and counseling, adherence counseling, medical exams, safety monitoring, short message system (SMS), ie text message, and peer support, panel management. |
|
| Baseline |
| Measure of changes in sexual risk taking behavior among Stay Study participants taking PrEP | Computer-Assisted Self-interview (CASI) data: Numbers of sexual partners, by serostatus and condom use, and anal/vaginal sex episodes, by partner serostatus, role of respondent, and condom use; sexually transmitted infection (STI) testing | 12 months |
| Measure of changes in STI among Stay Study participants taking PrEP | STI testing | 12 months |
| Side effects and toxicities of PrEP among study participants | Combined analysis of side effects and toxicities, including creatinine elevations | 12 months |
| PrEP discontinuations and reasons for discontinuation | PrEP discontinuations, reasons for discontinuation | 12 months |
| Differences in duration of PrEP use and study retention by sociodemographics, including race/ethnicity, age, education and risk practices | Combined analysis of CASI and interview data. | 15 months |
| The number of seroconversions and HIV drug resistance patterns among persons who become HIV infected in the project | HIV drug resistance patterns among persons who become infected | 12 months |
| Effects of PrEP on hormone levels | Combined analysis of hormone levels as relates to measures of adherence, such as TFV-DP in DBS, tenofovir levels in plasma | 12 months |
| The effect of hormone use on tenofovir-diphosphate concentrations among study participants | Combined analysis of hormone levels as relates to measures of adherence, such as TFV-DP in DBS, tenofovir levels in plasma | 12 months |
| Social harms experienced by study participants | Social Impact questionnaire | 12 months |
| Social benefits experienced by study participants | Social impact questionnaire | 12 months |
| Referrals to other HIV prevention services within the Stay Study | Combined analysis of CASI and interview data | 15 months |
| Access to and uptake of PrEP after project completion | Combined analysis of the proportion of participants interested in continuing PrEP and successfully able to access PrEP | 3 months |
| Acceptability and uptake of Stay Study PrEP support components | Combined analysis of CASI and interview responses. | 12 months |
| San Francisco |
| California |
| 94102 |
| United States |
| Tom Waddell Urban Health Clinic | San Francisco | California | 94102 | United States |
| San Francisco Community Health Clinic | San Francisco | California | 94109 | United States |
| Castro-Mission Health Center | San Francisco | California | 94114 | United States |
| ID | Term |
|---|---|
| D000069480 | Emtricitabine, Tenofovir Disoproxil Fumarate Drug Combination |
| ID | Term |
|---|---|
| D000068698 | Tenofovir |
| D063065 | Organophosphonates |
| D009943 | Organophosphorus Compounds |
| D009930 | Organic Chemicals |
| D000068679 | Emtricitabine |
| D003841 | Deoxycytidine |
| D003562 | Cytidine |
| D011741 | Pyrimidine Nucleosides |
| D011743 | Pyrimidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D000225 | Adenine |
| D011687 | Purines |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D003853 | Deoxyribonucleosides |
| D009705 | Nucleosides |
| D009706 | Nucleic Acids, Nucleotides, and Nucleosides |
| D004338 | Drug Combinations |
| D004364 | Pharmaceutical Preparations |
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