Trial reportImplementation science : IS2025
A pragmatic randomized trial to compare strategies for implementing primary HPV testing for routine cervical cancer screening in a large healthcare system.
Trial report in Implementation science : IS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04371887 (Comparing Strategies for Implementing Primary HPV Testing for Routine Cervical Cancer Screening), which is not on this map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Comparing Strategies for Implementing Primary HPV Testing for Routine Cervical Cancer Screening
Who cites it
2 citing papers in PubMed.
- An introduction to implementation science in rehabilitation medicine.PM & R : the journal of injury, function, and rehabilitation · 2025Article
- Locally-tailored vs. centrally-administered strategies for implementation of primary human papillomavirus (HPV) screening in an integrated healthcare system: a qualitative research study.Frontiers in health services · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
20 authors.
Funding
Abstract
backgroundRecent updates to national guidelines recommend primary human papillomavirus (HPV) screening for routine cervical cancer screening alongside previously recommended screening options. However, limited guidance exists for implementation approaches that best facilitate cancer screening practice substitution and achieve optimal stakeholder-centered outcomes. We compared "centrally-administered + locally-tailored" (here after referred to as locally-tailored) vs. "centrally-administered + usual care" (here after referred to as centrally-administered) approaches for achieving substitution of HPV and cytology co-testing with primary HPV screening for routine cervical cancer screening to examine the effect of local tailoring on implementation and stakeholder-centered outcomes.
methodsWe conducted a pragmatic, cluster randomized trial embedded in the Kaiser Permanente Southern California (KPSC) health system, randomly assigning site groups to study arms at the level of the geographic service area (12 service area randomized). The study took place between 2020-2022. Centrally-administered implementation strategy bundles included physician and staff educational activities. Sites in the locally-tailored arm underwent local needs assessment followed by local selection, tailoring and deployment of implementation strategy bundles. The primary outcome was the proportion of primary HPV screenings among all screenings performed. Secondary stakeholder-centered outcomes included patient (knowledge, emotional reaction, satisfaction, volume of patient inquiries) and provider outcomes (perception, knowledge, acceptance, and satisfaction) measured via repeated surveys or electronic health records. The generalized estimating equation framework and the difference-in-differences approach were used to compare outcomes across study arms.
resultsThe proportion of appropriate screenings (i.e., use of primary HPV screening) during the post-intervention period was high, with no observed difference between study arms: 98.4% (95% confidence interval [CI] 96.3%-100%) for the locally-tailored arm and 99.1% (95% CI: 97.8%-100%) for the centrally-administered arm (p = 0.34). There were no statistically or clinically significant differences in patient- and provider- outcomes between study arms.
conclusionsPrimary HPV screening was feasible and demonstrated high fidelity in all KPSC service areas. The locally-tailored practice substitution approach and centrally-administered practice substitution approach both achieved near complete uptake of primary HPV screening. Further, similar effects on stakeholder-centered outcomes were observed for both approaches. However, generalizability of our findings may be limited due to unique features of our integrated health system.
trial registrationNCT04371887. Registered 30 April 2020, URL: https://clinicaltrials.gov/study/NCT04371887?cond=primary%20HPV%20screening&rank=5 .
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