Parrying the Pitfalls of PrEP: Project PEACH
Parrying the Pitfalls of PrEP: Preventing Premature PrEP Discontinuation and STIs Among MSM
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Men who have sex with men (MSM) are disproportionately impacted by the U.S. HIV epidemic. Pre-exposure prophylaxis, or PrEP, is a relatively newer HIV prevention strategy that involves taking HIV antiviral medications either daily or on-demand to prevent HIV infection following high risk sexual activity. Both daily and on-demand PrEP have been shown to prevent infection if taken consistently and correctly. A prior research with this high-risk population in Atlanta, where it was offered daily PrEP to study participants, resulted in significant PrEP interest and initiation however high rates of PrEP discontinuation throughout the study were of great concern and, in some cases, led to HIV infection. Additionally, the study found high rates of bacterial sexually transmitted infection (STI) diagnoses both independent of, and concurrent with, higher PrEP use leading to concerns that condoms are not being used among MSM on PrEP.
The proposed work will expand upon the previous study with an intervention focus for MSM in Atlanta with aims of (1) preventing daily oral PrEP discontinuation; (2) offering on-demand oral PrEP as an alternative for MSM not interested in daily oral PrEP, (3) decreasing the incidence of bacterial STIs by offering STI post-exposure prophylaxis (PEP) which involves taking doxycycline immediately following high risk sexual behavior, 4) to start injectable PrEP as an alternative to daily oral PrEP or on-demand PrEP.
The study will involve a cohort of 200 MSM aged 18-45 in Atlanta who will be followed for two years. Participants will be recruited online from social media and dating websites, and in-person from different venues and events where MSM are known to attend. Men will take a short online eligibility screener either on a tablet, if recruited in-person, or on their own device if recruited online. Participants will be compensated for the various study activities (e.g., study visits, online behavioral surveys, weekly/monthly surveys).
If men screen eligible, they will be invited to a baseline study visit that will occur either in-person at the research clinic or virtually. Because of the ongoing COVID-19 pandemic, the plan is to offer participants the option of conducting study activities virtually or in-person. Consent will occur at the beginning of the baseline visit. Following the baseline visit, all participants will have two more study visits at months 12 and 24. At the three study visits, participants will be tested for HIV, STIs and drugs of abuse and take an online behavioral survey. Participants will also take an online behavioral survey at months 4, 7 and 19.
At all study visits, participants will discuss with the study counselor the various prevention options the study is offering-daily PrEP, on-demand PrEP, STI PEP or injectable PrEP as an alternative to daily oral PrEP or on-demand oral PrEP. If a participant elects to begin any of these, study staff will assist them in accessing oral PrEP from a community pharmacy and STI PEP (doxycycline) from the Emory Investigational Drug Service. Participants who start oral PrEP and/or STI PEP will take short weekly surveys for the first 2 weeks to monitor use and side effects. Following that 2-week period, daily oral PrEP users will get a monthly survey to try and detect warning signs of discontinuation so that the study can intervene to prevent that from happening. On-demand oral PrEP and STI PEP users will continue to get weekly surveys to monitor use and side effects. Oral PrEP and STI PEP users will have a 3-monthly visit-either in-person or virtually-to monitor their use and to test for HIV and STIs. Oral PrEP users will also have their kidney function monitored by creatinine testing. Participants electing to do their study activities virtually will be sent specimen collection kits so that they can self-collect specimens for all the required labs. They will mail back the specimens to the lab in a pre-paid postage mailer. Participants who elect injectable PrEP will be referred to local providers to access the medication; as part of our study, we will monitor their use through monthly surveys. Injectable PrEP Participants will have the option to switch prevention options at any point during the study by indicating their interest during monthly surveys or contacting study staff directly. Study clinicians will develop transition plan based on clinical indications.
All participants will be required to download the study app at the baseline visit and will be oriented to using it to retrieve study communication, surveys, lab results, etc. Additionally, the app will be used to schedule and conduct video conferencing sessions between participants and study clinicians/staff. If a participant reports warning signs of daily PrEP discontinuation, a peer navigator on staff will reach out through the app to try and schedule a counseling session that will use a motivational interviewing approach to support PrEP persistence.
The proposed work is of great significance for the field as novel approaches to preventing early discontinuation of PrEP are of utmost importance for preventing HIV transmission among MSM. If engaging with them frequently and assessing for warning signs of discontinuation is shown to be an effective strategy for intervening and preventing stoppage, then the implications for future interventions by community PrEP providers and clinicians is significant.
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 4
Contacts and Locations
Study Contact
Study Contact
- Name: Colleen Kelley, MD
- Phone Number: 404-712-1823
- Email: colleen.kelley@emory.edu
Study Contact Backup
- Name: Rebecca Moges, MPH
- Email: rebecca.moges-banks@emory.edu
Study Locations
-
-
Georgia
-
Atlanta, Georgia, United States, 30322
- PRISM Research Center
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male at birth
- Self-identify as Cisgender Male
- Ages 18-45 years
- ≥1 male anal sex partner in the 12 months before the baseline interview
- Live in the Atlanta MSA
- Owns cell phone with data service
- Willing to download a health-related app to their cell phone as part of the research study
- Able to provide ≥ 2 means of contact
- Not currently enrolled in another HIV prevention clinical trial
- Confirmed HIV-negative at baseline visit
Exclusion Criteria:
- Female at birth
- Do not self-identify as Cisgender Male
- Individuals < 18 years of age or > 45 years of age
- HIV positive status
- No male anal sex partner in the 12 months before the baseline interview
- Does not own mobile phone with data service
- Not willing to download a health-related app to their cell phone as part of the research study
- Live outside the metro Atlanta MSA and/or planning to move from Atlanta area in the next 2 years
- Currently enrolled in an HIV prevention or treatment clinical trial
- Adults unable to consent
- Individuals who are not yet adults (infants, children, teenagers)
- Pregnant women
- Prisoners
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: All men in cohort: MSM
Prospective cohort of MSM who are followed either in-person at the PRISM Health Research Clinic and/or virtually with remote study visits.
Participants will have the option to switch prevention options at any point during the study by indicating their interest during monthly surveys or contacting study staff directly.
|
Men taking daily oral PrEP (Truvada) will receive a monthly screener through the mobile app.
If answers to screener questions indicate a participant is at risk for PrEP discontinuation, then a peer navigator will deliver a motivational interviewing intervention and a clinician will consult with the participant.
These efforts are intended to avert PrEP discontinuation.
For men who are not interested in daily oral PrEP or plan to discontinue daily oral PrEP, the investigators will offer on-demand oral PrEP (Truvada) which will allow them to take it immediately before/after a sexual encounter.
It is hoped that this will serve as an alternative to daily oral PrEP use that is desirable for some people.
Other Names:
All men in the cohort will be offered STI PEP (doxycycline) to use after condomless sex with the goal of averting STI diagnoses.
At a dosage of 200 mg to be taken in a single dose ideally within 24 hours of possible exposure (e.g.
condomless anal sex) and no later than 72 hours after exposure.
Participants will be dispensed enough pills to allow for up to 3 weekly doses of 200mg doxycycline (i.e. 6 pills/week) for 3 months (the interval between STI testing visits).
Other Names:
For men who are interested in injectable PrEP, they will be referred to local providers to access Apretude (Cabotegravir injection) every two months.
In the study, their use of the medication will be monitored through monthly surveys during which they have the option to indicate interest in switching to oral PrEP.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Men Who Discontinue Daily Oral PrEP
Time Frame: 24 month post intervention
|
MSM taking daily oral PrEP will complete monthly screener surveys delivered through study app to assess for PrEP stop intentions.
After early identification, they will receive Motivational Interviewing (MI) to avoid discontinuation.
Participants that discontinue PrEP will be measured.
|
24 month post intervention
|
|
Number of Men Who Initiate On-demand Oral PrEP
Time Frame: 24 month post intervention
|
MSM who decline daily oral PrEP will be prescribed TDF/FTC fixed dose combination, 2 doses 2-24 hrs before sex and single dose 24 and 48 hours after first dose.
|
24 month post intervention
|
|
Number of Men Who Initiate Long-acting Injectable PrEP
Time Frame: 24 month post intervention
|
Number of men who are not interested in daily oral PrEP or on-demand oral PrEP will be offered Long-acting injectable PrEP through referral to outside providers.
|
24 month post intervention
|
|
Number of STI Diagnoses
Time Frame: Baseline, 12 and 24 months post intervention
|
All men in cohort will be evaluated for STI diagnoses at baseline, 12 and 24 month post intervention.
|
Baseline, 12 and 24 months post intervention
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Investigators
Investigators
- Principal Investigator: Patrick Sullivan, MD, Emory University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Urogenital Diseases
- Genital Diseases
- Pathologic Processes
- Disease Attributes
- Infections
- Communicable Diseases
- Pathological Conditions, Signs and Symptoms
- Sexually Transmitted Diseases
- Organic Chemicals
- Heterocyclic Compounds, 1-Ring
- Heterocyclic Compounds
- Heterocyclic Compounds, 2-Ring
- Heterocyclic Compounds, Fused-Ring
- Pharmaceutical Preparations
- Nucleic Acids, Nucleotides, and Nucleosides
- Hydrocarbons
- Hydrocarbons, Cyclic
- Polycyclic Aromatic Hydrocarbons
- Hydrocarbons, Aromatic
- Polycyclic Compounds
- Purines
- Deoxycytidine
- Cytidine
- Pyrimidine Nucleosides
- Pyrimidines
- Organophosphorus Compounds
- Nucleosides
- Naphthacenes
- Tetracyclines
- Deoxyribonucleosides
- Organophosphonates
- Adenine
- Drug Combinations
- Tenofovir
- Emtricitabine
- Emtricitabine, Tenofovir Disoproxil Fumarate Drug Combination
- Doxycycline
- cabotegravir
Other Study ID Numbers
Other Study ID Numbers
- STUDY00000608
- 5R01MH123724-02 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
Researchers who provide a methodologically sound proposal, to achieve aims in the approved proposal.
Proposals should be directed to pssulli@emory.edu. To gain access, data requestor will need to sign a data access agreement.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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