Project PEACH is a prospective, observational cohort of 240 people assigned male sex at birth who have sex with other men (MSM) living in metropolitan Atlanta, Georgia. Recruitment of the cohort took place from November 2021 to September 2023. Participants are followed for 2 years with study assessments at baseline and months 4, 7, 12, 19, and 24. Study inclusion and exclusion criteria are shown in Textbox 1.

All participants were offered daily PrEP with tenofovir disoproxil fumarate (TDF) 300 mg/emtricitabine (FTC) 200 mg unless the participant had underlying chronic kidney disease with a creatinine clearance <50 mL/min or other contraindication for TDF/FTC per clinician review, in which case the participant was offered daily tenofovir alafenamide 25 mg/FTC 200 mg. All participants were also offered STI PEP with doxycycline 200 mg to be taken no longer than 72 hours after condomless sex. Participants who elected to use STI PEP were dispensed enough doxycycline to allow up to three weekly doses, but refills were readily available to participants if requested. If a participant was not interested in daily PrEP or planned to discontinue daily PrEP, they were offered on-demand PrEP. On-demand PrEP was offered with TDF/FTC and participants were directed to take two pills 2-24 hours before sex and to take an additional pill 24 hours after the first pill and a final dose 24 hours after that (“2-1-1”). TDF/FTC and tenofovir alafenamide/FTC prescriptions were provided for use at local pharmacies and navigation for insurance approvals and patient assistance plans for uninsured participants or participants with copays were provided. We amended our study protocol in May 2022 when injectable PrEP with cabotegravir became locally available. Patients were offered this option through local partner community organizations by providing them with information about clinics and instructing them to make an appointment, although injectable PrEP remained difficult to access throughout the study period. Participants were able to elect to start PrEP or STI PEP or change PrEP modality at each survey visit (months 4, 7, 12, and 19) or at any time through the study app.

All participants were provided with the study’s mobile SMaRT (Study Management and Retention Toolkit) phone app to support early identification of risks for PrEP discontinuation and offer alternative prevention methods, to identify any side effects from medications, to provide information about STI PEP and document use patterns of on-demand PrEP and STI PEP, and to support easy linkage to support services for PrEP counseling and addressing concerns or questions about STI PEP. Participants are able to complete monthly (daily PrEP and injectable PrEP users) and weekly (on-demand PrEP, STI PEP, and first 2 weeks for daily PrEP users) short surveys within the SMaRT app, which also provides links to web-based study assessments at months 4, 7, 12, 19, and 24.

Participant recruitment was conducted through multiple sources. We used a modified venue-day-time screening approach using data from past studies to prioritize venues with historically high numbers of MSM who were HIV-negative [27,28]. We offered a US $5 incentive to take the study screener at in-person recruitment events. We used dating apps and social media with targeted advertisements to adult MSM in Atlanta and offered US $20 incentives to current study participants who shared our institutional review board (IRB)–approved study ads on their social media. Our initial recruitment plan was to exclude participants already on PrEP, but given limitations in enrollment during the COVID-19 pandemic, we expanded eligibility in May 2022 to include participants currently prescribed PrEP. NIH recruitment goals were set to include ≥70% of participants who identify as a racial or ethnic minority, including ≥10% of all participants identifying as Hispanic.

Participants who were eligible for the study based on the initial screening questionnaire were scheduled for an enrollment (baseline) visit at the community-based Programs, Research, & Innovation in Sexual Minority Health (PRISM) Health Research Clinic. This clinical site is located 1.5 blocks from public transportation, and ride-share services were provided to participants with limited transportation opportunities or long commutes. The enrollment visit consisted of an informed consent process, a computer-assisted self-interview behavioral survey, HIV and STI testing, training on using the study app, and a counseling session to include pre- and posttest HIV prevention information and a discussion about PrEP and STI PEP options. Participants who completed an enrollment visit were compensated US $125 regardless of whether they subsequently participated in the study. Participants with a positive HIV screening test at baseline or any point during the study were linked to HIV care.

To maximize retention, we used several strategies. We hired a study staff member dedicated exclusively to retention who collaborated with the study team to promote retention among participants. The SMaRT mobile app was customized for this study to allow participants to schedule, reschedule, receive reminders of, and cancel study appointments; communicate securely with study staff; and update contact information from within the Health Insurance Portability and Accountability Act (HIPAA)-compliant app. Participants were reminded about their follow-up visits through the app messaging system or their preferred means of contact both 3 days and 1 day before the scheduled follow-up date. We also sent reminders for surveys up to one week prior and up to 20 days after the target date through the SMaRT app. If we lost contact with participants (missed surveys or appointments and were nonresponsive to contact requests), we obtained consent to use for-fee public-use databases (eg, Lexis-Nexis) to locate participants; this has been used by us in previous studies to relocate participants who were lost to follow-up [29,30]. For participants who could not be contacted, after IRB approval, staff first attempted to contact emergency contacts, and if unsuccessful, attempted to link the identities of participants to registries of known decedents using a statewide data set (vital records) and a nationwide data set (National Death Index).

All participants who elected to use oral PrEP or STI PEP received brief weekly surveys for the first two weeks after starting medications, with a US $5 incentive provided for each survey. After this period, daily PrEP and injectable PrEP users received monthly short surveys to assess risk for discontinuation (US $10 incentive for each survey) whereas participants who opted for on-demand PrEP or STI PEP continued to receive weekly short surveys (US $5 incentive for each survey). All participants were sent computer-assisted self-interview surveys at months 4, 7, 12, 19, and 24, and encouraged to attend in-person follow-up visits at 12 and 24 months (US $40 at 4, 7, and 19 months; US $100 at 12/24-month survey and study visit) and additional telehealth or in-clinic visits if the risk for PrEP discontinuation was identified by surveys. Daily or on-demand PrEP users or STI PEP users had the option for in-person or home-testing for HIV/STIs every 3 months for clinical monitoring of their medication use. For injectable PrEP users, all clinical monitoring was done outside the study by a local provider of the participants’ choosing.

Risk factors for discontinuing PrEP were developed using data from a previous cohort of MSM in Atlanta (Textbox 2) [14,31,32]. When a participant reported any of these risk factors for discontinuing PrEP on a monthly survey, they were invited to schedule a discussion with a peer navigator with the intention of identifying possible risks for PrEP discontinuation, minimizing discontinuation of PrEP, or offering another prevention option. Triage sessions were client-centered, using an approach grounded in motivational interviewing. By focusing on the last time that the client was confident about being on PrEP (eg, think back to when you were taking your medication every day, what was going on in your life? Where were you living? Who were you dating?), the peer navigators were able to better understand the holistic context of the current risk factor. Based on this comprehensive understanding of needs and the monthly screening data, trained peer navigators used motivational interviewing tools to help participants problem-solve based on the needs identified and worked with them to develop a plan to address those concerns while maintaining PrEP, if appropriate. Clinical concerns (eg, side effects) were referred to a PrEP clinician for discussion.

Laboratory testing was done at the research clinic or remotely by the participant at home using self-collection specimen methods and differed by prevention method choice as described in Table 1. Clinical monitoring of injectable PrEP use was done by the local provider who administered the medication. Any positive HIV/STI test results were provided to participants over the phone by a study staff member who could refer participants to study-paid treatment for STI infections at a local community-based health clinic, or to participant-paid treatment through a provider of their choosing. Negative test results were delivered through the HIPPA-compliant study app. To minimize bias in self-report data on substance use, we collected urine drug screening in our on-site clinical laboratory improvement amendments-waived laboratory at baseline, 12, and 24 months using the Ten Panel Integrated EZ Split Key Cup Drug Test. We attempted to examine Neisseria gonorrhoeae resistance patterns among men who acquired the infection during follow-up by having them return for Neisseria gonorrhoeae culture prior to treatment with compensation of US $100; however, we discontinued this when none of the isolates grew in culture.

In Table 2, we have outlined the proposed analyses for this study. We will evaluate the rate of PrEP uptake, rate of doxyPEP uptake, rate of PrEP discontinuation, rate of doxyPEP discontinuation, and rate of incident STI and HIV diagnoses by prevention choice. We will describe use patterns of PrEP modality and STI PEP over the study period including changes in use. We will also describe the proportion of participants who initially chose each method of PrEP and the proportion who switched method of PrEP during the study period. We will describe the utilization of various support systems offered. Finally, we will compare incident STI diagnoses (gonorrhea, chlamydia, syphilis) at 12 and 24 months in this cohort to a historical control group to evaluate the effect of STI PEP.

The study was approved by the Emory IRB (STUDY00000608). Informed consent was provided by participants at the time of enrollment and participants were given the option to opt out of the study at any time. The data obtained were all anonymized using a unique patient identifier number. Participants were compensated for their time as outlined above.

Given the ongoing HIV and STI syndemic, there is a great need to leverage available tools to help prevent these infections. We designed this study to investigate the preference for HIV and STI prevention strategies and support mechanisms among MSM in Atlanta, Georgia. After the enrollment of 240 men, we found that their initial choice of prevention was typically daily PrEP combined with doxyPEP. Of all prevention methods, combining PrEP with doxyPEP was more desirable than doxyPEP alone. To our knowledge, this is the first study to evaluate the preference for a combination of PrEP and doxyPEP. Participants will be followed longitudinally for 24 months to evaluate the persistence of these prevention interventions and changes in preferences over time. Strengths of this study include that we have recruited a racially and ethnically diverse cohort of participants with two-year longitudinal follow-up, and its novel design to evaluate how patient preferences change over time.

In several prior studies of preference for PrEP modality, individuals have prioritized PrEP effectiveness and low-cost options; as more long-acting PrEP options become available, recent studies have demonstrated that this is often desirable, but that preference for long-acting PrEP may differ between groups [21,33,34]. During enrollment in this study, long-acting injectable PrEP with cabotegravir was approved in the United States for HIV prevention. Although we incorporated this change into our study protocol, there were delays in clinics being able to offer this option to patients, leading to a few participants selecting this as their initial choice. Given this, although it appeared very few people chose injectable PrEP initially, this is likely not representative of true choices given the initial lack of availability. We anticipate that individuals may change their preferences for using PrEP and STI prevention methods based on factors like sexual practices and that motivational interviewing through this study can assist participants persist or reengage in using prevention methods.

There are a few limitations to this study. Although initial results suggest a preference for daily oral PrEP combined with doxyPEP, injectable PrEP was not yet available at the time of enrollment for most individuals; this preference may be different in the era of injectable PrEP. Individuals were eligible for the study only if they lived in metropolitan Atlanta, so conclusions from this study may be different for populations in different geographic areas. Although the study was open to all individuals regardless of insurance status, nearly 70% of participants were insured, which may have affected the choice of STI prevention method. Given that this is an observational study, there is potential for unmeasured bias.

We plan to evaluate the preferences of combination PrEP and doxyPEP over the course of 2 years and describe trends including changes in use over time. We also plan to evaluate the impact of support tools like motivational imaging on the persistence of sexual health prevention methods. Bundling PrEP and doxyPEP in a way to be most desirable and acceptable to MSM, along with determining what support tools augment persistence, will be imperative to curb the HIV and STI syndemic, which is particularly pronounced in the southern United States. We plan to present the findings of our work at community advisory board meetings, community-oriented presentations, and through peer-reviewed publications, with the goal of ensuring patients are supported in choosing a combination of sexual health prevention methods that are best for their needs.