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Evaluation of Implementation of the Phoenix PrEP (Pre-Exposure Prophylaxis) Access Project for Youth Aged 13-24

Evaluation of Implementation of the Phoenix PrEP Access Project for Youth Aged 13-24

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03637322
Enrollment
42
Registered
2018-08-20
Start date
2018-06-01
Completion date
2022-12-31
Last updated
2023-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

IV Drug Usage, Unsafe Sex

Brief summary

This study will evaluate the implementation of a PrEP program for youth aged 13-24 in Phoenix, AZ. Numbers of youth who initiate PrEP, how long they continue with PrEP, and the barriers for youth who are trying to initiate and continue taking PrEP will be examined.

Detailed description

This observational study will describe the barriers encountered and the benefits found as youth engage in a PrEP program, the Phoenix PrEP Access Project and as they participate in PrEP provided through standard medical care. This study does not investigate the safety, efficacy or other medical benefits of PrEP, but looks at the issues surrounding youth who are trying to access PrEP.

Interventions

None listed

Sponsors

Phoenix Children's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
13 Years to 24 Years
Healthy volunteers
No

Inclusion criteria

* sexually active youth aged 13 through 24, * at risk for contracting HIV, * Negative for HIV as indicated by Negative Elisa and Western Blot (WB) or Negative 4th Generation test, * weight greater than 35kg, * offered PrEP to reduce the risk of contracting HIV.

Exclusion criteria

* Unknown or Positive HIV status, * Renal Impairment as indicated by elevated BUN or Creatinine, abnormal urinalysis, * Active infection with Hepatitis B Virus, * Taking other medications containing Emtricitabine, Tenofovir or tenofovir alafenamide(TAF) such as Atripla, Complera, Emtriva, Genvoya, Odefsey, Stribild, and Viread taking drugs containing lamivudine, * taking Hepsera, * clinical symptoms consistent with acute viral infection within the past month.

Design outcomes

Primary

MeasureTime frameDescription
PrEP Uptake3 yearsUptake of PrEP offered to youth presenting for PrEP ages 13-24

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026