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NCT05365048 · ClinicalTrials.gov registry record · NA
Provider Recommendation and HPV Vaccination
A NA study of Human Papilloma Virus, sponsored by Kaiser Permanente.
- Recruiting
- Registry status
- NA
- Development phase
- 301,201
- Enrollment target
- 1
- Study location
NCT05365048: Recruiting NA study of Human Papilloma Virus, sponsored by Kaiser Permanente.
NCT05365048 is a NA study of Human Papilloma Virus that is actively recruiting participants, run by Kaiser Permanente. The registered enrollment target is 301,201 participants, above the 718-participant average among 39 other Human Papilloma Virus trials with a reported enrollment target (41850% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05365048, a NA study of Human Papilloma Virus, is actively recruiting participants, sponsored by Kaiser Permanente.
- RECRUITING
- Registry status
- NA
- Development phase
- 301,201 participants
- Enrollment target
- 1
- Study location
Study Summary
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 imp
Primary Outcome
9-12 years old who received the first dose of the HPV vaccine at pre-intervention. Data obtained from electronic medical record (EMR)
Conditions Studied
Interventions
- OTHER Local Tailoring implementation strategy
- OTHER Prescribed Strategy
Study Locations (1)
California
- Kaiser Permanente Southern California - Pasadena
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 301,201 participants |
| Start Date | 2022-03-21 |
| Est. Completion | 2026-06-30 |
| Phase | NA |
What NCT05365048 shows while recruiting
NCT05365048 is an interventional study that assigns participants to a tested intervention. Its 301,201 participants enrollment target places it among the larger protocols in the corpus, above the 718-participant average among 39 other Human Papilloma Virus trials with a reported enrollment target (41850% higher).
The record links to 1 condition, with Human Papilloma Virus appearing as the primary indexed condition, and to 2 interventions - of which Local Tailoring implementation strategy is the first listed.
NCT05365048 reports a single indexed study location in California.
Frequently Asked Questions
What is clinical trial NCT05365048 about?
NCT05365048 is a clinical study titled "Provider Recommendation and HPV Vaccination". 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...
What is the current status of trial NCT05365048?
This trial is currently recruiting. It is a NA study. The enrollment target is 301,201 participants. The study started on 2022-03-21. Estimated completion is 2026-06-30.
What conditions does trial NCT05365048 study?
This clinical trial studies the following conditions: Human Papilloma Virus.
What interventions are being tested in trial NCT05365048?
The interventions under investigation include: Local Tailoring implementation strategy (OTHER), Prescribed Strategy (OTHER).
Who is sponsoring clinical trial NCT05365048?
This trial is sponsored by Kaiser Permanente, which has 294 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05365048 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT05365048's enrollment target sits among peer trials
301,201 1st of 39 higher than 39 of 39 other Human Papilloma Virus trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Human Papilloma Virus trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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