Actively Recruiting
Provider Recommendation and HPV Vaccination
Led by Kaiser Permanente · Updated on 2025-05-20
301201
Participants Needed
1
Research Sites
223 weeks
Total Duration
On this page
Sponsors
K
Kaiser Permanente
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
In the United State, there are millions of US teens who are not vaccinated against the human papillomavirus (HPV) putting them at risk of getting HPV-related cancers. Although there are clinical guidelines recommending the HPV vaccine and interventions encouraging parents to vaccinate their children to prevent HPV-related cancers, the vaccination rate for teens remains low according to a 2018 national survey. Survey data shows that HPV vaccine complete series coverage for teens aged 13-15 years was 50%, far below the 80% target of Healthy People 2020. Receiving a strong provider recommendation is the most powerful strategy for improving HPV vaccine rates. Yet, little is known about how to include provider recommendations and other important factors into an intervention to improve the HPV vaccination rates. Studies show there are provider, patient and system-level barriers in the initiation and completion of HPV vaccine series among 9-12 years old children. Barriers to the HPV vaccine also differ across demographic subgroups, communities, and clinics. Interventions that address only one component are not responsive to site barriers and as effective as one that addresses multiple components and site-specific barriers. This study uses a 3-arm cluster randomized controlled trial (RCT) to compare three implementation strategies to improve provider recommendations on the HPV vaccine. Two of the implementation strategies (local-tailored and prescribed strategy) utilize a multilevel approach. The three implementation strategies of interest are (1) a "local-tailored" implementation strategy, co-designed with local care teams to address local barriers and contexts (2) A "prescribed" strategy, most commonly used by health systems, that involves pre-specified interventions addressing pre-selected vaccination barriers and (3) usual standard of care where there are no research-led activities. We will use surveys, interviews, and electronic health records to evaluate the three implementation strategies and their impact on improving HPV vaccination rates. The study surveys and interviews will include pediatric providers, nurses, administrators, staff members, and parents of HPV vaccine-eligible children (9-12 years old). Successful implementation will be defined as improvement in HPV vaccination rates (primary outcome), strengthening provider recommendation (secondary outcome), and the cost-effectiveness of the implementation strategy.
CONDITIONS
Official Title
Provider Recommendation and HPV Vaccination
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All KPSC pediatric clinics
- All providers (physicians, nurses, and medical assistants) and department administrators from the pediatric department
- Parents of HPV vaccine-eligible children (9-12 years old)
You will not qualify if you...
- Providers and administrators who do not work for the pediatric department
- Parents of children older than 12 years and/or who did not have a clinic visit in the study period
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Kaiser Permanente Southern California
Pasadena, California, United States, 91101
Actively Recruiting
Research Team
N
Nancy Takahashi Cannnizzaro, PhD
CONTACT
C
Chunyi Hsu, MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
3
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