Sexually Transmitted Infections (Not HIV or Hepatitis)SHARPNCT07361926
Sexual Health Access at Retail Pharmacies: Advancing Pharmacy-based Delivery of Primary STI and HIV Prevention for Cisgender Women
A study testing doxy-PEP, Serial STI testing and HIV PEP/PrEP in people with Sexually Transmitted Infections (Not HIV or Hepatitis) and HIV Infections, run by University of Washington.
Trial summary
This proposed 3-arm randomized study will compare different pharmacy based approaches that include HIV prevention medication (PrEP and PEP), routine STI testing, and preventive antibiotic (doxycycline) for STIs. Read more about this study
- Who is it for?
- Ages 15 to 24 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Sexually Transmitted Infections (Not HIV or Hepatitis), HIV Infections
- What is being tested?
- doxy-PEP, Serial STI testing and HIV PEP/PrEP
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 720 participants
- Where
- No sites listed yet
- Study dates
- May 2026to Jun 2030
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 15 to 24 years
- Women only
- Healthy volunteers accepted
- Child, Adult
Who may be able to join
- Cis-gender female
- Seeking contraception (emergency contraception, oral contraceptive pills, injectables, implants, and condoms) from the retail pharmacy site
- Age ≥ 15 and <25 years old
- Willingness to receive PrEP screening per national guidelines including HIV testing
- Not currently taking PrEP
- Planning to reside in the area for the next 12 months
- Able and willing to provide informed consent for participation
Who cannot join
- Current participation in other ongoing studies.
- Medical contraindications to PrEP or doxycycline use (e.g., severe allergy to doxycycline, serious hepatic or renal disease).
- Any other condition that, in the investigator's judgment, would make participation unsafe or interfere with study procedures.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
This proposed 3-arm randomized study will compare different pharmacy based approaches that include HIV prevention medication (PrEP and PEP), routine STI testing, and preventive antibiotic (doxycycline) for STIs. The study will assess how well these services can be implemented, how acceptable they are to young women, and whether they are cost-effective.
Read the detailed description
Global incidence of STIs increased over the past decade, with over one million curable STIs acquired daily. In 2020, the World Health Organization (WHO) estimated 374 million new infections of Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), Trichomonas vaginalis (TV), and syphilis. Young women in East Africa face high prevalence of curable STIs and HIV,4 and high STI incidence. Studies confirm higher STI prevalence among younger women compared to their male peers, and older women. STIs severely affect mortality and morbidity for cisgender women by causing tubal infertility, chronic pelvic pain, pelvic inflammatory disease, ectopic pregnancy, postpartum endometriosis, adverse neonatal outcomes, and increased susceptibility to HIV. In HIV high-burden settings, cultural, economic, and social marginalization of women contributes to the risk of HIV and STIs,10 in part by making condom use negotiation challenging. Despite high STI burden in these settings, research to address STIs lags behind HIV in young cisgender women.
WHO calls for vastly increasing STI testing and integrating STI interventions to reach priority populations.Sexually transmitted infections (STIs) disproportionately affect cisgender adolescent girls and young women (AGYW) who often experience STI complications, including infertility, chronic pelvic pain, and increased risk for HIV acquisition and peripartum morbidity. In Kenya, HIV and STIs comprise a syndemic with 40% of new HIV infections occurring among AGYW. Yet, research to address STIs lags behind HIV in this priority population and no primary STI prevention tools are currently available to cisgender women beyond condoms. In Kenya, 40% of women access contraception without interfacing with facilities, including at retail pharmacies, and are missed by facility-based HIV services like pre-exposure prophylaxis (PrEP). In the ongoing work among AGYW seeking contraception at 20 pharmacies in Kisumu, Kenya (NCT05467306); all AGYW offered STI testing accepted, 29% had CT or NG, and 70% accepted expedited partner therapy (EPT) and report no social harms. Among AGYW seeking emergency contraception, only 3% previously used HIV post-exposure prophylaxis (PEP), highlighting an opportunity to offer HIV PEP to AGYW via pharmacies. Qualitative data suggest that STI testing motivates health promoting behaviors, even when STI results are negative.
To date, no studies evaluate if serial STI testing promotes PrEP persistence. 'Event-driven' doxycycline PEP (doxy-PEP) for CT, NG, and syphilis found no protective benefit for Kenyan women accessing PrEP at facilities, likely due to low adherence. AGYW more frequently access emergency contraception at pharmacies compared to facilities; thus, 'event-driven' strategies, like HIV PEP ("PEP-in-Pocket") or doxy-PEP, may have higher use in pharmacies. The investigators propose a RCT in Kisumu, Kenya-a region with 11% HIV prevalence-to test co-offering HIV PEP/PrEP and STI testing with and without doxy-PEP in pharmacies and prospectively assess HIV PEP/PrEP use and persistence, and STI incidence among AGYW (n=720) and estimate cost and cost-effectiveness of this strategy. The investigators hypothesize that expanding HIV and STI prevention options to include HIV PEP, STI testing, EPT, and doxy-PEP in pharmacies will be cost-effective and improve HIV and STI outcomes in AGYW, a population disproportionately affected by STIs and HIV. The study is designed to inform pharmacy delivery of biomedical HIV and STI prevention services and provide evidence to inform policy for STI/HIV prevention among AGYW.
- Being tested
- doxy-PEP, Serial STI testing, HIV PEP/PrEP
- Keywords
- STI prevention, HIV prevention, Pharmacy delivery
- Medical subject headings
- Sexually Transmitted Diseases, Hepatitis, HIV Infections
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
doxy-PEPDrug
Also called doxycycline
Antiobiotic for post exposure prophylaxis
Serial STI testingDiagnostic test
CT/NG and syphilis testing
HIV PEP/PrEPDrug
HIV post and pre exposure prophylaxis
| Study group | Role | What they receive |
|---|---|---|
| Serial STI testing and doxy-PEP | Active comparator | STI testing and doxy-PEP offered with HIV PEP/PrEP services Receives: Drug: doxy-PEP; Diagnostic Test: Serial STI testing; Drug: HIV PEP/PrEP |
| Serial STI testing alone | Active comparator | STI testing offered with HIV PEP/PrEP Receives: Diagnostic Test: Serial STI testing; Drug: HIV PEP/PrEP |
| No serial STI testing or doxy-PEP | Active comparator | HIV PEP/PrEP services only Receives: Drug: HIV PEP/PrEP |
What is being measured
The primary outcome is the main question the study is designed to answer.
HIV PrEP initiation
HIV PrEP initiation among women seeking contraception at retail pharmacies defined as accepting either daily oral PrEP pills or the DPV-VR when offered at enrollment and evidence of self-reported use at 1-month post-acceptance
Measured: From enrollment to the end of participant follow up after 12 months
HIV PrEP persistence
PrEP persistence defined as continuing with HIV PrEP use at 12-months
Measured: From enrollment to the end of participant follow up at 12 months
STI incidence
STI incidence (CT, NG, and/or syphilis)
Measured: From enrollment to the end of participant follow up at 12 months
Secondary outcomes (4)
HIV PEP, PrEP method selection
Self-selection of DPV-VR, daily PrEP, and/or PEP when offered at enrollment compared across all randomization arms
Measured: From enrollment to the end of participant follow up at 12 months
HIV PrEP following PEP
Initiating HIV PrEP at anytime of the study following prior HIV PEP use
Measured: From enrollment to the end of participant follow up at 12 months
HIV PrEP adherence
Detectable TFC levels in hair at 12 month visit
Measured: At end of participant follow up at 12 months
Predictors of non-adherence
Factors associated with poor adherence (<90% adherence on PrEP or discontinuation)
Measured: From enrollment through the end of participant follow up at 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Jan 2026
- Study startMay 2026 (estimated)
- Primary completionJun 2029 (estimated)
- Study completionJun 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Sexually Transmitted Infections (Not HIV or Hepatitis)Studies of the same condition, open and under way.
- More trials run by University of WashingtonThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- 3 arm, non blinded, individually randomized controlled trial to compare 1) HIV PEP/PrEP plus serial STI testing and non doxy-PEP, 2) HIV PEP/PrEP plus serial STI testing alone, and 3) HIV PEP/PrEP only, with embedded mixed-methods implementation and economic evaluation components.
- Masking
- None (open label)
- Enrolment
- 720 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Washington
- Sponsor type
- University, hospital or other
- Collaborators
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH)
- Responsible party
- Principal investigator, Jillian Pintye, University of Washington
- Investigators
- Jillian Pintye, PhD, Principal investigator, University of Washington
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07361926
- Sponsor's protocol ID
- STUDY00022204
- Other IDs
- R01HD118713
- Acronym
- SHARP
- Status last verified
- Jan 2026
- First submitted
- 21 Jan 2026
- Last updated
- 28 Jan 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 28 Jan 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Sexual Health Access at Retail Pharmacies: Advancing Pharmacy-based Delivery of Primary STI and HIV Prevention for Cisgender Women
- ClinicalTrials.gov ID
- NCT07361926
- Acronym / sponsor ID
- SHARP / STUDY00022204
- Keywords
- STI prevention, HIV prevention, Pharmacy delivery
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 720 participants (estimated)
- Lead sponsor
- University of WashingtonUniversity, hospital or other
- Collaborators
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH)
- Study start
- May 2026 (estimated)
- Primary completion
- Jun 2029 (estimated)
- Study completion
- Jun 2030 (estimated)
- First posted
- 23 Jan 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This proposed 3-arm randomized study will compare different pharmacy based approaches that include HIV prevention medication (PrEP and PEP), routine STI testing, and preventive antibiotic (doxycycline) for STIs. The study will assess how well these services can be implemented, how acceptable they are to young women, and whether they are cost-effective.
Detailed description
Global incidence of STIs increased over the past decade, with over one million curable STIs acquired daily. In 2020, the World Health Organization (WHO) estimated 374 million new infections of Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), Trichomonas vaginalis (TV), and syphilis. Young women in East Africa face high prevalence of curable STIs and HIV,4 and high STI incidence. Studies confirm higher STI prevalence among younger women compared to their male peers, and older women. STIs severely affect mortality and morbidity for cisgender women by causing tubal infertility, chronic pelvic pain, pelvic inflammatory disease, ectopic pregnancy, postpartum endometriosis, adverse neonatal outcomes, and increased susceptibility to HIV. In HIV high-burden settings, cultural, economic, and social marginalization of women contributes to the risk of HIV and STIs,10 in part by making condom use negotiation challenging. Despite high STI burden in these settings, research to address STIs lags behind HIV in young cisgender women.
WHO calls for vastly increasing STI testing and integrating STI interventions to reach priority populations.Sexually transmitted infections (STIs) disproportionately affect cisgender adolescent girls and young women (AGYW) who often experience STI complications, including infertility, chronic pelvic pain, and increased risk for HIV acquisition and peripartum morbidity. In Kenya, HIV and STIs comprise a syndemic with 40% of new HIV infections occurring among AGYW. Yet, research to address STIs lags behind HIV in this priority population and no primary STI prevention tools are currently available to cisgender women beyond condoms. In Kenya, 40% of women access contraception without interfacing with facilities, including at retail pharmacies, and are missed by facility-based HIV services like pre-exposure prophylaxis (PrEP). In the ongoing work among AGYW seeking contraception at 20 pharmacies in Kisumu, Kenya (NCT05467306); all AGYW offered STI testing accepted, 29% had CT or NG, and 70% accepted expedited partner therapy (EPT) and report no social harms. Among AGYW seeking emergency contraception, only 3% previously used HIV post-exposure prophylaxis (PEP), highlighting an opportunity to offer HIV PEP to AGYW via pharmacies. Qualitative data suggest that STI testing motivates health promoting behaviors, even when STI results are negative.
To date, no studies evaluate if serial STI testing promotes PrEP persistence. 'Event-driven' doxycycline PEP (doxy-PEP) for CT, NG, and syphilis found no protective benefit for Kenyan women accessing PrEP at facilities, likely due to low adherence. AGYW more frequently access emergency contraception at pharmacies compared to facilities; thus, 'event-driven' strategies, like HIV PEP ("PEP-in-Pocket") or doxy-PEP, may have higher use in pharmacies. The investigators propose a RCT in Kisumu, Kenya-a region with 11% HIV prevalence-to test co-offering HIV PEP/PrEP and STI testing with and without doxy-PEP in pharmacies and prospectively assess HIV PEP/PrEP use and persistence, and STI incidence among AGYW (n=720) and estimate cost and cost-effectiveness of this strategy. The investigators hypothesize that expanding HIV and STI prevention options to include HIV PEP, STI testing, EPT, and doxy-PEP in pharmacies will be cost-effective and improve HIV and STI outcomes in AGYW, a population disproportionately affected by STIs and HIV. The study is designed to inform pharmacy delivery of biomedical HIV and STI prevention services and provide evidence to inform policy for STI/HIV prevention among AGYW.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
- Model description
- 3 arm, non blinded, individually randomized controlled trial to compare 1) HIV PEP/PrEP plus serial STI testing and non doxy-PEP, 2) HIV PEP/PrEP plus serial STI testing alone, and 3) HIV PEP/PrEP only, with embedded mixed-methods implementation and economic evaluation components.
| Arm | Type | Receives |
|---|---|---|
| Serial STI testing and doxy-PEP | Active comparator | Drug: doxy-PEP, Diagnostic Test: Serial STI testing, Drug: HIV PEP/PrEPSTI testing and doxy-PEP offered with HIV PEP/PrEP services |
| Serial STI testing alone | Active comparator | Diagnostic Test: Serial STI testing, Drug: HIV PEP/PrEPSTI testing offered with HIV PEP/PrEP |
| No serial STI testing or doxy-PEP | Active comparator | Drug: HIV PEP/PrEPHIV PEP/PrEP services only |
Who may qualify
- Ages
- 15 to 24 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (7 listed)
- Cis-gender female
- Seeking contraception (emergency contraception, oral contraceptive pills, injectables, implants, and condoms) from the retail pharmacy site
- Age ≥ 15 and <25 years old
- Willingness to receive PrEP screening per national guidelines including HIV testing
- Not currently taking PrEP
Key exclusion criteria (3 listed)
- Current participation in other ongoing studies.
- Medical contraindications to PrEP or doxycycline use (e.g., severe allergy to doxycycline, serious hepatic or renal disease).
- Any other condition that, in the investigator's judgment, would make participation unsafe or interfere with study procedures.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| doxy-PEPAlso: doxycyclineAntiobiotic for post exposure prophylaxis | Drug | Serial STI testing and doxy-PEP |
| Serial STI testingCT/NG and syphilis testing | Diagnostic test | Serial STI testing alone, Serial STI testing and doxy-PEP |
| HIV PEP/PrEPHIV post and pre exposure prophylaxis | Drug | No serial STI testing or doxy-PEP, Serial STI testing alone, Serial STI testing and doxy-PEP |
Primary outcome
HIV PrEP initiation
Time frame: From enrollment to the end of participant follow up after 12 months
HIV PrEP initiation among women seeking contraception at retail pharmacies defined as accepting either daily oral PrEP pills or the DPV-VR when offered at enrollment and evidence of self-reported use at 1-month post-acceptance
HIV PrEP persistence
Time frame: From enrollment to the end of participant follow up at 12 months
PrEP persistence defined as continuing with HIV PrEP use at 12-months
STI incidence
Time frame: From enrollment to the end of participant follow up at 12 months
STI incidence (CT, NG, and/or syphilis)
4 secondary outcomes
HIV PEP, PrEP method selection
Time frame: From enrollment to the end of participant follow up at 12 months
HIV PrEP following PEP
Time frame: From enrollment to the end of participant follow up at 12 months
HIV PrEP adherence
Time frame: At end of participant follow up at 12 months
Predictors of non-adherence
Time frame: From enrollment through the end of participant follow up at 12 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Jan 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Jillian Pintye, PhD principal investigator
University of Washington
Questions about this trial
What is this clinical trial studying?
A study testing doxy-PEP, Serial STI testing and HIV PEP/PrEP in people with Sexually Transmitted Infections (Not HIV or Hepatitis) and HIV Infections, run by University of Washington.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 28 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Meena Lenn, MPH (206.543.7140, mlenn@uw.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
HIV PrEP initiation (time frame: From enrollment to the end of participant follow up after 12 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Jan 2026; AzTrials last refreshed its copy on 26 Oct 2026.