- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03442062
Quality Improvement Strategies to Increase Human Papillomavirus (HPV) Vaccination
May 7, 2020 updated by: University of North Carolina, Chapel Hill
Impact of AFIX and Physician-to-Physician Engagement on HPV Vaccination in Primary Care: A Randomized Controlled Trial
HPV vaccination is at lower levels than the national goals.
This study will evaluate the effectiveness of quality improvement strategies for increasing HPV vaccination coverage among adolescents in primary care clinics.
Study Overview
Status
Completed
Conditions
Detailed Description
The University of North Carolina will test the effectiveness of the Center for Disease Control and Prevention's AFIX model, physician-to-physician engagement, and both strategies in combination, for increasing HPV vaccination coverage among adolescents in primary care clinics.
AFIX (Assessment, Feedback, Incentives and eXchange) consists of brief quality improvement consultations that immunization specialists from state health departments deliver to vaccine providers in primary care settings.
Using immunization registry data, the specialist evaluates the clinic's vaccination coverage and delivers education on best practices to improve coverage.
Physician-to-physician (P2P) engagement consists of physician educators providing feedback about clinics' current HPV vaccination coverage and in-depth training about how to make strong and effective HPV vaccination recommendations to primary care providers via remote webinar consultations.
Physician educators will also use immunization registry data to provide feedback on clinics' vaccine coverage.
The investigators will compare changes in HPV vaccination coverage before and after intervention for high-volume primary care clinics in four study conditions: AFIX consultations delivered in-person by state health department immunization specialists (AFIX group), physician-to-physician consultations delivered remotely by trained physician educators (P2P group), both AFIX and P2P consultations in combination (AFIX + P2P group), or no HPV quality improvement intervention (control group).
In each state, 30 clinics will be randomly assigned to each study arm, for a total of 120 clinics per state, or 360 clinics overall.
As a secondary endpoint, we proposed to evaluate the impact of intervention "booster" visits delivered at 12-months post-intervention.
However, the CDC has recently changed the AFIX program so that the desired comparison is no longer possible.
Therefore, we have eliminated booster visits.
This change does not affect our primary endpoint.
The primary objective of this study is to compare the change in coverage for HPV vaccine initiation among 11-12 year old patients, from baseline to 12-month follow-up.
Secondarily, the study will compare the change in coverage for other vaccines, age groups and time periods.
Study Type
Interventional
Enrollment (Actual)
264
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Arizona
-
Phoenix, Arizona, United States, 85007
- Arizona Department of Health Services
-
-
New York
-
Albany, New York, United States, 12237
- New York State Department of Health
-
-
Wisconsin
-
Madison, Wisconsin, United States, 53703
- Wisconsin Department of Health Services
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Pediatric or family medicine clinics or practices in New York, Wisconsin, or Arizona with at least 200 active records for patients, ages 11-17, in their states' immunization information systems.
Exclusion Criteria:
- Less than 200 active records for patients between 11-17
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: AFIX
Clinics randomly assigned to this arm will receive an Assessment Feedback Incentives and eXchange (AFIX) consultation delivered in-person by a state health department immunization specialist.This arm includes ~ 90 high-volume primary care clinics in three states (New York, Wisconsin, Arizona).
|
The adolescent AFIX (Assessment, Feedback, Incentives, and eXchange) Program is a quality improvement strategy developed by the CDC to improve the immunization practices and vaccination coverage levels of public and private health care providers.
It has four main components: 1) Assessment of a provider's current immunization practices and vaccination levels, 2) Feedback of the assessment results and strategies to improve coverage levels, 3) Incentives to improve coverage levels, and 4) eXchange of information and resources necessary to facilitate improvement.
Relevant AFIX information will be communicated to vaccine providers using several intervention and quality improvement components.
Other Names:
|
|
Experimental: Physician-to-physician engagement
Clinics randomly assigned to this arm will receive physician-to-physician (P2P) consultations delivered remotely to providers by physician educators.
This arm includes ~90 high-volume primary care clinics in three states (New York, Wisconsin, Arizona).
|
Physician-to-physician engagement is a quality improvement strategy in which trained physician educators deliver a 60 minute consultation via interactive webinar.
The consultations will be delivered to providers in primary care clinics and will include didactic instruction on HPV-related cancers, HPV vaccination, communication training, and assessment and feedback about each clinics' vaccination coverage.
Other Names:
|
|
Experimental: AFIX + P2P
Clinics randomly assigned to this arm will receive both an Assessment Feedback Incentives and eXchange (AFIX) consultation and a physician-to-physician (P2P) consultation.This arm includes ~90 high-volume primary care clinics in three states (New York, Wisconsin, Arizona).
|
The adolescent AFIX (Assessment, Feedback, Incentives, and eXchange) Program is a quality improvement strategy developed by the CDC to improve the immunization practices and vaccination coverage levels of public and private health care providers.
It has four main components: 1) Assessment of a provider's current immunization practices and vaccination levels, 2) Feedback of the assessment results and strategies to improve coverage levels, 3) Incentives to improve coverage levels, and 4) eXchange of information and resources necessary to facilitate improvement.
Relevant AFIX information will be communicated to vaccine providers using several intervention and quality improvement components.
Other Names:
Physician-to-physician engagement is a quality improvement strategy in which trained physician educators deliver a 60 minute consultation via interactive webinar.
The consultations will be delivered to providers in primary care clinics and will include didactic instruction on HPV-related cancers, HPV vaccination, communication training, and assessment and feedback about each clinics' vaccination coverage.
Other Names:
|
|
Other: Active Intervention Control
Clinics randomly assigned to this arm will receive a brief non-HPV vaccine related quality improvement consultation.
This arm includes ~90 high-volume primary care clinics in three states (New York, Wisconsin, Arizona).
|
Active Intervention Control will be a remotely delivered quality improvement strategy on a clinical topic other than HPV vaccination.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
HPV vaccination (≥1 dose), 11-12 year olds at 12 months
Time Frame: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine initiation (≥1 dose), among 11- to 12- year old patients, as measured by states' immunization information system (IIS) records
|
Twelve months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
HPV vaccination (completion according to the Advisory Committee on Immunization Practices (ACIP) guidelines), 11-12 year olds at six months
Time Frame: Six months
|
Coverage change from baseline to six months in HPV vaccine completion, among 11- to 12- year-old patients, as measured by states' IIS records
|
Six months
|
|
HPV vaccination (≥1 dose), 13-17 year olds at six months
Time Frame: Six months
|
Coverage change from baseline to six months in HPV vaccine initiation (≥1 dose), among 13- to 17- year-old patients, as measured by states' IIS records
|
Six months
|
|
HPV vaccination (completion according to ACIP guidelines), 13-17 year olds at six months
Time Frame: Six months
|
Coverage change from baseline to six months in HPV vaccine completion, among 13- to 17- year-old patients, as measured by states' IIS records
|
Six months
|
|
HPV vaccination (≥1 dose), 11-12 year olds at 6 months
Time Frame: Six months
|
Coverage change from baseline to six months in HPV vaccine initiation (≥1 dose), among 11- to 12- year-old patients, as measured by states' IIS records
|
Six months
|
|
HPV vaccination (≥1 dose), 11-12 year olds at six months by state
Time Frame: Six months
|
Coverage change from baseline to six months in HPV vaccine initiation (≥1 dose), among 11- to 12- year-old patients, as measured by states' IIS records, stratifying by state (NY, WI or AZ)
|
Six months
|
|
HPV vaccination (≥1 dose), 11-12 year olds at 12 months by state
Time Frame: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine initiation (≥1 dose), among 11- to 12- year-old patients, as measured by states' IIS records, stratifying by state (NY, WI or AZ)
|
Twelve months
|
|
HPV vaccination (≥1 dose), 11-12 year olds at 18 months
Time Frame: Eighteen months
|
Coverage change from baseline to eighteen months in HPV vaccine initiation (≥1 dose), among 11- to 12- year-old patients, as measured by states' IIS records
|
Eighteen months
|
|
HPV vaccination (≥1 dose), 11-12 year olds at 18 months by state
Time Frame: Eighteen months
|
Coverage change from baseline to eighteen months in HPV vaccine initiation (≥1 dose), among 11- to 12- year-old patients, as measured by states' IIS records, stratifying by state (NY, WI, or AZ).
|
Eighteen months
|
|
HPV vaccination (completion according to ACIP guidelines), 11-12 year olds at six months by state
Time Frame: Six months
|
Coverage change from baseline to six months in HPV vaccine completion, among 11- to 12- year-old patients, as measured by states' IIS records, stratifying by state (NY, WI, or AZ)
|
Six months
|
|
HPV vaccination (completion according to ACIP guidelines), 11-12 year olds at 12 months
Time Frame: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine completion, among 11- to 12- year-old patients, as measured by states' IIS records
|
Twelve months
|
|
HPV vaccination (completion according to ACIP guidelines), 11-12 year olds at 12 months by state
Time Frame: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine completion, among 11- to 12- year-old patients, as measured by states' IIS records, stratifying by state (NY, WI, or AZ)
|
Twelve months
|
|
HPV vaccination (completion according to ACIP guidelines), 11-12 year olds at 18 months
Time Frame: Eighteen months
|
Coverage change from baseline to eighteen months in HPV vaccine completion, among 11- to 12- year-old patients, as measured by states' IIS records
|
Eighteen months
|
|
HPV vaccination (completion according to ACIP guidelines), 11-12 year olds at 18 months by state
Time Frame: Eighteen months
|
Coverage change from baseline to eighteen months in HPV vaccine completion, among 11- to 12- year-old patients, as measured by states' IIS records, stratifying by state (NY, WI, AZ)
|
Eighteen months
|
|
HPV vaccination (≥1 dose), 13-17 year olds at 12 months
Time Frame: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine initiation (≥1 dose), among 13- to 17- year-old patients, as measured by states' IIS records
|
Twelve months
|
|
HPV vaccination (≥1 dose), 13-17 year olds at 18 months
Time Frame: Eighteen months
|
Coverage change from baseline to eighteen months in HPV vaccine initiation (≥1 dose), among 13- to 17- year-old patients, as measured by states' IIS records
|
Eighteen months
|
|
HPV vaccination (completion according to ACIP guidelines), 13-17 year olds at 12 months
Time Frame: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine completion, among 13- to 17- year-old patients, as measured by states' IIS records
|
Twelve months
|
|
HPV vaccination (completion according to ACIP guidelines), 13-17 year olds at 18 months
Time Frame: Eighteen months
|
Coverage change from baseline to eighteen months in HPV vaccine completion, among 13- to 17- year-old patients, as measured by states' IIS records
|
Eighteen months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Tetanus, diphtheria, and acellular pertussis (Tdap) vaccination, 11-12 year olds
Time Frame: Twelve months
|
Coverage change from baseline to twelve months in Tdap vaccination among 11- to 12-year-old patients, as measured by states' IIS records
|
Twelve months
|
|
Meningococcal vaccination (≥1 dose), 11-12 year olds
Time Frame: Twelve months
|
Coverage change from baseline to twelve months in meningococcal vaccination (≥1 dose), among 11- to 12- year-old patients, as measured by states' IIS records
|
Twelve months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Noel T Brewer, PhD, University of North Carolina
- Principal Investigator: Melissa B Gilkey, PhD, University of North Carolina
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 7, 2018
Primary Completion (Actual)
April 30, 2020
Study Completion (Actual)
April 30, 2020
Study Registration Dates
First Submitted
February 15, 2018
First Submitted That Met QC Criteria
February 21, 2018
First Posted (Actual)
February 22, 2018
Study Record Updates
Last Update Posted (Actual)
May 11, 2020
Last Update Submitted That Met QC Criteria
May 7, 2020
Last Verified
May 1, 2020
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 18-0146a
- 1U01IP001073-01 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Human Papillomavirus Infection
-
The AlfredMerck Sharp & Dohme LLCCompletedHuman Papillomavirus Infection | Human PapillomavirusAustralia
-
Daré Bioscience, Inc.Advanced Research Projects Agency for Health (ARPA-H)Not yet recruitingHuman Papilloma Virus (HPV) | High-risk Human Papillomavirus InfectionUnited States
-
Centre Hospitalier Universitaire de BesanconCompletedHuman Papillomavirus InfectionFrance
-
University Hospital, GenevaCompletedHuman Papillomavirus InfectionSwitzerland
-
University of ConnecticutCompletedHuman Papillomavirus Infection
-
Indiana UniversityMerck Sharp & Dohme LLCUnknownHuman Papillomavirus InfectionUnited States
-
Gen-Probe, IncorporatedCompletedHuman Papillomavirus InfectionUnited States
-
GlaxoSmithKlineCompletedHuman Papillomavirus Infection
-
GlaxoSmithKlineCompletedHuman Papillomavirus InfectionEgypt
-
University Hospital, GenevaUnknown
Clinical Trials on Assessment Feedback Incentives and eXchange
-
University of North Carolina, Chapel HillNorth Carolina Division of Public HealthCompletedImmunization | Adolescent Health ServicesUnited States
-
University of North Carolina, Chapel HillHarvard Medical School (HMS and HSDM); Robert Wood Johnson Foundation; Michigan... and other collaboratorsCompletedPapillomavirus Vaccines | Adolescent Health ServicesUnited States
-
Drexel UniversityAmerican College of Sports Medicine; Psi Chi; QualtricsCompletedPhysical Activity | Sedentary Lifestyle | Overweight and ObesityUnited States
-
Brown UniversityCompletedObesity | Physical ActivityUnited States
-
Massachusetts General HospitalRobert Wood Johnson FoundationCompletedFood LabelingUnited States
-
Children's Hospital of PhiladelphiaNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Boston... and other collaboratorsCompletedSpina Bifida | Kidney TransplantUnited States
-
University of PennsylvaniaNational Institute on Aging (NIA)Completed
-
Drexel UniversityAmerican College of Sports Medicine; Psi Chi; QualtricsCompletedObesity | Overweight | Physical Activity | Sedentary Lifestyle
-
University of PennsylvaniaNational Institute on Aging (NIA)Completed
-
San Diego State UniversityNational Heart, Lung, and Blood Institute (NHLBI)CompletedLung Diseases | AsthmaUnited States