AzTrials
AzTrials

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.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
Search all trials

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
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.

Meena Lenn, MPH contact

206.543.7140

mlenn@uw.edu

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 groups in NCT07361926
Study groupRoleWhat they receive
Serial STI testing and doxy-PEPActive comparatorSTI 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 aloneActive comparatorSTI testing offered with HIV PEP/PrEP
Receives: Diagnostic Test: Serial STI testing; Drug: HIV PEP/PrEP
No serial STI testing or doxy-PEPActive comparatorHIV 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.

  1. 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

  2. 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

  3. 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)
  1. 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

  2. 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

  3. HIV PrEP adherence

    Detectable TFC levels in hair at 12 month visit

    Measured: At end of participant follow up at 12 months

  4. 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.

  1. First posted23 Jan 2026
  2. Study startMay 2026 (estimated)
  3. Primary completionJun 2029 (estimated)
  4. Study completionJun 2030 (estimated)

Resources

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)
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

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.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in