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NCT05065840Active, not recruiting

Advancing HPV Vaccination Among HIV Positive Adults: The CHAMPS Study

Implementing an Evidence-Based, Multilevel Intervention to Promote HPV Vaccination Among HIV Positive Adults

Source: ClinicalTrials.gov · Last updated 14 May 2026

Brief summary (registry, in English)

People living with HIV (PLWH) are 28 times more likely to be diagnosed with Human Papillomavirus (HPV) - associated anal cancer than the general population. The HPV vaccine is an effective and safe approach to prevent and reduce the risk of HPV-related disease among PLWH. HPV vaccine programs tailored and implemented in the HIV population are lagging for this high-risk group. The CDC's 4 Pillars Transformation Program is a multi-level, evidence-based intervention that has been successfully used to increase HPV vaccination in the general population and is ready to be tested in the high-risk HIV population, particularly PLWH in the rural South. This program offers providers and clinic staff evidence-based strategies to increase HPV vaccination uptake via training and educational resources. This study proposes to tailor and refine the 4 Pillars Program and conduct this project in three HIV clinics in Georgia.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
267 (actual)
First submitted
22 Sept 2021
Start date
22 May 2023
Primary completion date
1 Feb 2028
Lead sponsor
Emory University
Diseases
HIV
NCT number
NCT05065840

What you commit to

  • Study type: Interventional
  • Participants enrolled: 267
  • From 22 May 2023 to the primary completion date, 1 Feb 2028
  • 4 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

  • Has contraindications to receiving the HPV vaccine i.e., history of an anaphylactic allergy to latex, an immediate hypersensitivity to yeast, current moderate or severe acute illness, and/or are currently pregnant)

Who the study is looking for

  • HIV positive
  • 18-45 years of age
  • Can read and speak English
  • Capable of providing informed consent
  • Has not previously received three series HPV vaccine
  • No contraindications to receiving HPV vaccine (i.e. history of anaphylactic allergy to later, an immediate hypersensitivity to yeast, current moderate or severe acute illness, and/or are currently pregnant).

Age in the registry: 18 years to 45 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

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

SiteCityCountrySite status
Albany Rural Model Clinic
Coordinator of this site? Confirm its status
AlbanyUnited StatesUnknown status
AID Atlanta
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
Faebris
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
AHF Lithonia
Coordinator of this site? Confirm its status
LithoniaUnited StatesUnknown status

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