AFIX to Improve HPV Vaccination (AFIX)
23. Februar 2017 aktualisiert von: University of North Carolina, Chapel Hill
Adolescent AFIX: A Multi-state RCT to Increase Adolescent Vaccination by Facilitating Providers' Adoption of Best Practices
The University of North Carolina will test the effectiveness of the Centers for Disease Control and Prevention's AFIX model for increasing HPV vaccination coverage among adolescents.
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.
We will compare changes in HPV vaccination coverage before and after consultations for high-volume pediatric and family medicine clinics across three study conditions: traditional consultations (in-person group), virtual consultations (webinar group), or no consultations (control group).
In each participating state, 30 clinics will be randomly assigned to each study arm, for a total of 90 clinics per state, or 270 clinics overall.
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 6-month follow-up.
Secondarily, we will compare the change in coverage for other vaccines and age groups.
Studienübersicht
Status
Abgeschlossen
Bedingungen
Intervention / Behandlung
Studientyp
Interventionell
Einschreibung (Tatsächlich)
223
Phase
- Unzutreffend
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
-
-
Illinois
-
Springfield, Illinois, Vereinigte Staaten, 62761
- Illinois Department of Public Health
-
-
Michigan
-
Lansing, Michigan, Vereinigte Staaten, 48909
- Michigan Department of Community Health
-
-
North Carolina
-
Chapel Hill, North Carolina, Vereinigte Staaten, 27599
- University of North Carolina
-
-
Washington
-
Olympia, Washington, Vereinigte Staaten, 98504
- Washington State Department of Health
-
-
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Kind
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Ja
Studienberechtigte Geschlechter
Alle
Beschreibung
Inclusion Criteria: Pediatric or family medicine clinics or practices in WA, IL, or MI with
- at least 500 active records for patients, ages 11-17, in their states' immunization information systems.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Versorgungsforschung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Kein Eingriff: control
This arm includes 30 high-volume primary care clinics in each of three states (Washington, Illinois, Michigan) for a total of 90 clinics.
Clinics randomly assigned to this arm will receive no AFIX consultation.
|
|
|
Experimental: AFIX in-person consultation
This arm includes 30 high-volume primary care clinics in each of three states (Washington, Illinois, Michigan) for a total of 90 clinics.
Clinics randomly assigned to this arm will receive an in-person AFIX consultation.
Consultations will be delivered by state health department staff.
|
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.
Andere Namen:
|
|
Experimental: AFIX webinar consultation
This arm includes 30 high-volume primary care clinics in each of three states (Washington, Illinois, Michigan) for a total of 90.
Clinics randomly assigned to this arm will receive an AFIX consultation via interactive webinar.
Consultations will be delivered by state health department staff.
|
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.
Andere Namen:
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
HPV vaccination (≥1 dose), 11-12 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in HPV vaccine initiation (≥1 dose), among 11- to 12-year old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by electronic immunization information system (IIS) records, controlling for child's sex
|
Six months
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
HPV vaccination (≥1 dose), 11-12 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in HPV vaccine initiation (≥1 dose), among 11- 12-year old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records, stratifying by child's sex.
|
Six months
|
|
HPV vaccination (≥1 dose), 11-12 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in HPV vaccine initiation (≥1 dose), among 11- to 12-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records, stratifying by state (IL, MI or WA).
|
Six months
|
|
HPV vaccination (≥1 dose), 11-12 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine initiation (≥1 dose), among 11- to 12-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records, stratifying by child's sex.
|
Twelve months
|
|
HPV vaccination (≥1 dose), 11-12 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine initiation (≥1 dose), among 11- to 12-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records, stratifying by state (IL, MI or WA).
|
Twelve months
|
|
HPV vaccination (3 doses), 11-12 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in HPV vaccine completion (3 doses), among 11- to 12-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Six months
|
|
Tetanus, diphtheria, and acellular pertussis (Tdap) vaccination, 11-12 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in Tdap vaccination among 11- to 12-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Six months
|
|
Meningococcal vaccination (≥1 dose), 11-12 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in meningococcal vaccination (≥1 dose), among 11- to 12-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Six months
|
|
HPV vaccination (≥1 dose), 13-17 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in HPV vaccine initiation (≥1 dose), among 13- to 17-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Six months
|
|
HPV vaccination (3 doses), 13-17 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in HPV vaccine completion (3 doses), among 13- to 17-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Six months
|
|
Tdap vaccination, 13-17 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in Tdap vaccination among 13- to 17-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Six months
|
|
Meningococcal vaccination (≥1 dose), 13-17 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in meningococcal vaccination (≥1 dose), among 13- to 17-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Six months
|
|
HPV vaccination (≥1 dose), 11-12 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine initiation (≥1 dose), among 11- to 12-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Twelve months
|
|
HPV vaccination (3 doses), 11-12 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine completion (3 doses), among 11- to 12-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Twelve months
|
|
Tdap vaccination, 11-12 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in Tdap vaccination among 11- to 12-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Twelve months
|
|
Meningococcal vaccination (≥1 dose), 11-12 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in meningococcal vaccination (≥1 dose), among 11- to 12-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Twelve months
|
|
HPV vaccination (≥1 dose), 13-17 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine initiation (≥1 dose), among 13- to 17-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Twelve months
|
|
HPV vaccination (3 doses), 13-17 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine completion (3 doses), among 13- to 17-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Twelve months
|
|
Tdap vaccination, 13-17 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in Tdap vaccination among 13- to 17-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Twelve months
|
|
Meningococcal vaccination (≥1 dose), 13-17 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in meningococcal vaccination (≥1 dose), among 13- to 17-year-old patients in the control arm versus the combined in-person and webinar intervention arms, as measured by IIS records.
|
Twelve months
|
|
HPV vaccination (≥1 dose), 11-12 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in HPV vaccine initiation (≥1 dose), among 11- to 12-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Six months
|
|
HPV vaccination (3 doses), 11-12 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in HPV vaccine completion (3 doses), among 11- to 12-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Six months
|
|
Tdap vaccination, 11-12 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in Tdap vaccination among 11- to 12-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Six months
|
|
Meningococcal vaccination (≥1 dose), 11-12 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in meningococcal vaccination (≥1 dose), among 11- to 12-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Six months
|
|
HPV vaccination (≥1 dose), 13-17 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in HPV vaccine initiation (≥1 dose), among 13- to 17-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Six months
|
|
HPV vaccination (3 doses), 13-17 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in HPV vaccine completion (3 doses), among 13- to 17-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Six months
|
|
Tdap vaccination, 13-17 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in Tdap vaccination among 13- to 17-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Six months
|
|
Meningococcal vaccination (≥1 dose), 13-17 year olds
Zeitfenster: Six months
|
Coverage change from baseline to six months in meningococcal vaccination (≥1 dose), among 13- to 17-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Six months
|
|
HPV vaccination (≥1 dose), 11-12 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine initiation (≥1 dose), among 11- to 12-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Twelve months
|
|
HPV vaccination (3 doses), 11-12 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine completion (3 doses), among 11- to 12-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Twelve months
|
|
Tdap vaccination, 11-12 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in Tdap vaccination among 11- to 12-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Twelve months
|
|
Meningococcal vaccination (≥1 dose), 11-12 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in meningococcal vaccination (≥1 dose), among 11- to 12-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Twelve months
|
|
HPV vaccination (≥1 dose), 13-17 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine initiation (≥1 dose), among 13- to 17-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Twelve months
|
|
HPV vaccination (3 doses), 13-17 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in HPV vaccine completion (3 doses), among 13- to 17-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Twelve months
|
|
Tdap vaccination, 13-17 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in Tdap vaccination among 13- to 17-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Twelve months
|
|
Meningococcal vaccination (≥1 dose), 13-17 year olds
Zeitfenster: Twelve months
|
Coverage change from baseline to twelve months in meningococcal vaccination (≥1 dose), among 13- to 17-year-old patients in the webinar versus in-person intervention arm, as measured by IIS records.
|
Twelve months
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Mitarbeiter
Ermittler
- Hauptermittler: Noel T Brewer, PhD, University of North Carolina
- Hauptermittler: Melissa B Gilkey, PhD, Harvard Medical School (HMS and HSDM)
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn
1. April 2015
Primärer Abschluss (Tatsächlich)
1. November 2016
Studienabschluss (Tatsächlich)
1. November 2016
Studienanmeldedaten
Zuerst eingereicht
5. Februar 2015
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
24. Februar 2015
Zuerst gepostet (Schätzen)
25. Februar 2015
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
24. Februar 2017
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
23. Februar 2017
Zuletzt verifiziert
1. Februar 2017
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Andere Studien-ID-Nummern
- 13-3599
- 71272 (Andere Zuschuss-/Finanzierungsnummer: Robert Wood Johnson Foundation)
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
NEIN
Beschreibung des IPD-Plans
No raw data will be shared with the general public or other researchers.
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .