Clinical trial Recruiting at 1 site Interventional Ages 12 to 30

Improving HIV treatment options for youth

Official title: Strategies to AchieVe Viral Suppression for Youth With HIV (The SAVVY Study)

Run by Johns Hopkins University · NCT06886971 · Data updated 2026-11-12

This study is testing if personalized treatment options and counseling can help young people with HIV better manage their condition and improve their health.

Quick facts

Study typeInterventional
Ages12 Years to 30 Years
SexAll
Enrollment288 (estimated)
SponsorJohns Hopkins University
Academic / other
Locations1 site (Baltimore, Maryland)
StatusRecruiting
StartedNovember 10, 2024
Main results expectedNovember 15, 2027
Study endsJuly 31, 2028
Registry record updatedFebruary 4, 2026
Trial IDNCT06886971 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adolescents and young adults aged 12-30 who are prescribed antiretroviral therapy and are willing to engage in shared decision-making about their treatment.

Probably not a fit

Patients with relevant drug resistance mutations, severe mental health issues, or those planning to relocate within the next year may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The SAVVY Study focuses on enhancing viral suppression in adolescents and young adults living with HIV by optimizing their antiretroviral treatment choices. It employs CHOICE counseling to engage participants in shared decision-making regarding their preferred treatment options, including long-acting injectable antiretroviral therapies. The study addresses unique challenges faced by this population, such as cognitive development and psychosocial factors, to improve adherence and health outcomes. By providing tailored interventions and access to alternative treatment strategies, the study aims to significantly improve virologic outcomes for participants.

Why it matters

Potential benefit: If successful, this study could lead to improved viral suppression rates among adolescents and young adults with HIV, enhancing their overall health and reducing public health risks.

How similar studies have gone: Other studies have shown promise in improving treatment adherence and outcomes for youth with HIV using similar engagement and treatment strategies, indicating that this approach is both relevant and potentially effective.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* prescribed ART,
* willing to sign informed consent (including communication with one's primary HIV provider)

Exclusion Criteria:

* Relevant drug resistance mutations (per medical record) that compromises activity of Cabotegravir (CBG) + rilpivirine (RPV)
* disallowed medications,
* pregnancy.
* Mental health, cognitive, or behavioral dysfunction that in the opinion of the site PI would impair participation;
* severe illness/hospitalization at the time of enrollment,
* plan to move away in the next 12 months.

Where it's running

  • Johns Hopkins University
    Baltimore, Maryland, United States
    Recruiting

Study contacts

  • Principal investigator: Allison Agwu, MD, SCM — Johns Hopkins University
  • Study coordinator: Allison Agwu, MD, SCM
  • Email: ageorg10@jhmi.edu
  • Phone: 410-614-3917

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.