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NCT07510048Recruiting

Combatting HIV Or Other STIs Early (CHOOSE)

Combatting HIV Or Other STIs Early (CHOOSE): An Integrated Strategy of Pre-Exposure Prophylaxis (PrEP) Mobile Health (mHealth) Support and Doxycycline Post-Exposure Prophylaxis (DoxyPEP)

Source: ClinicalTrials.gov · Last updated 9 Oct 2026

Brief summary (registry, in English)

The overarching goal of this project is to optimize the PrEP Choice integrated mHealth package and assess the efficacy and cost of PrEP Choice on PrEP initiation and adherence among young people. It is hypothesized that PrEP Choice will improve HIV PrEP uptake and adherence among young people and will be cost-effective to deliver to young people in the United States (U.S.). This study will also assess the uptake, adherence, and acceptability of DoxyPEP among young people.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
200 (estimated)
First submitted
24 Feb 2026
Start date
16 Sept 2026
Primary completion date
30 Mar 2029
Lead sponsor
Westat
Diseases
HIV
NCT number
NCT07510048

What you commit to

  • Study type: Interventional
  • Planned participants: 200
  • From 16 Sept 2026 to the primary completion date, 30 Mar 2029
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Currently participating in an interventional trial of PrEP agents, or prior enrollment in HPTN 083, HPTN 083-01, or any other study of long-acting PrEP (including PURPOSE- 2 lenacapavir study);
  • Any concurrent participation in other clinical trials or behavioral intervention studies without prior approval from the protocol team.

Other illness

  • In a mutually monogamous sexual relationship with a partner not living with HIV for the past 12 months;
  • Any other medical, behavioral, or other conditions that in the opinion of the SC Project Lead could interfere with adherence to study procedures or the individual's ability to remain in the study for an 18-month period or compromise interpretation of study results.

Other

  • Female;
  • Plan to move within 18 months to an area inaccessible to a participating ATN SC;
  • An employee of the participating SC; or

Who the study is looking for

  • Age 13-24 years, inclusive;
  • Self-reports being at increased likelihood for HIV acquisition, defined as having anal sex with a male in their lifetime;
  • Owns an iOS or Android Smartphone and able to access all elements of the PrEP Choice package;
  • Not currently on PrEP and interested in learning more about PrEP;
  • Is not living with HIV;
  • Weighs at least 35 kg;
  • Willing to receive PrEP care from a provider at a participating ATN SC;
  • Able to understand, read, and speak English;
  • Able to participate at the study site; and
  • Willing and able to provide written informed consent.
  • If of legal age or otherwise able to provide independent informed consent as determined by local law and consistent with IRB policies: Willing and able to provide written informed consent for study participation.
  • If not of legal age or otherwise not able to provide independent informed consent as determined by local law and consistent with IRB policies: Parent or legal guardian is willing and able to provide written informed consent for study participation and potential participant is willing and able to provide written assent for study participation.

Age in the registry: 13 years to 24 years · Sex: Male · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Illinois Chicago
Coordinator of this site? Confirm its status
ChicagoUnited StatesRecruiting
St. Jude Children's Research Hospital
Coordinator of this site? Confirm its status
MemphisUnited StatesRecruiting
Tulane University
Coordinator of this site? Confirm its status
New OrleansUnited StatesRecruiting
San Francisco Department of Public Health
Coordinator of this site? Confirm its status
San FranciscoUnited StatesRecruiting
University of South Florida
Coordinator of this site? Confirm its status
TampaUnited StatesRecruiting
Children's National Medical Center
Coordinator of this site? Confirm its status
Washington D.C.United StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.