Recruiting

STOP-HPV-Online & STOP-HPV-LC

Sponsor:

UCLA

Code:

NCT06831383

Conditions

Human Papilloma Virus Vaccine

Eligibility Criteria

Sex: All

Age: 9 - 17

Healthy Volunteers: Not accepted

Interventions

STOP-HPV-Online

STOP-HPV-LC

Study Details

Brief summary:

Human papillomavirus (HPV) causes 35,900 US cancer cases per year, 4,000 deaths, and $4 billion in can In this study, the investigators will conduct a 3-arm clustered randomized controlled trial (RCT) in an estimated 72 practices from up to 8 health systems to evaluate the effectiveness and cost effectiveness of two potentially scalable implementation strategies (based on prior work) to increase the initiation of HPV vaccine against a usual care (control) arm. The intervention arms are 1) online provider communication training only ("STOP-HPV-Online" and 2) online provider communication training plus a Learning Collaborative, with performance feedback, attended by practice leads ("STOP-HPV-LC).

cer-related costs. It is recommended at ages 11-12 years routinely but can be given starting at ages 9-10 years. Despite having an effective vaccine, HPV vaccine initiation/completion rates in the U.S. were only at 76.8%/61.4% respectively in 2023 among 13-17 year olds; these rates are lower than the other recommended adolescent vaccines. Two key barriers are 1) suboptimal clinician communication to address parental concerns and 2) ineffective office systems causing missed vaccine opportunities.

Conditions

Human Papilloma Virus Vaccine

Study ID

NCT06831383

Start date

Mar 30, 2026

Status verified date

Feb, 2026

Completion date

Apr 19, 2027

Anticipated

Primary completion date

Apr 19, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 9 - 17

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Patient of participating practice
  • Well child care visit during the 12-month intervention period
  • No prior dose of HPV vaccine at the time of the well child care visit
  • Age-eligible

Exclusion Criteria:

  • Prior dose of HPV vaccine

Study Design

Enrollment

100000 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Health Services Research

Interventions and Outcome Measures

Arms

experimental: STOP-HPV Online

Provider communication training

experimental: STOP-HPV LC

Provider communication training plus Learning Collaborative sessions attended by practice leads and quarterly performance feedback to the practice.

no intervention: Usual Care

Standard of care control

Interventions

STOP-HPV-Online

Approximately one third of practices within a participating health system will be randomized to receiving the STOP-HPV-Online intervention.

STOP-HPV-LC

Approximately one third of practices within a participating health system will be randomized to receiving the STOP-HPV-LC intervention.

Primary outcome measure

  • Initiation (first dose) of HPV vaccination among 9-<13 year olds at or following a well care visit with a participating provider during the intervention period. [ Time Frame: 12 months from start of intervention ]

Central Contacts and Locations

Central contacts

Christina Albertin, PhD, MPH

317-701-4926calbertin@mednet.ucla.edu

Locations

AMGA

Recruiting

Alexandria, Virginia, United States, 22314

Contacts

More Information

Sponsor

University of California, Los Angeles

Last update posted

May 19, 2026

Last verified

Feb, 2026

Keywords

  • Human Papillomavirus Vaccination
  • Practice-based improvement

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of California, Los Angeles on 2026-05-19.