- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01159093
Giving Immunizations Through Vaccine Education (GIVE)
11. marts 2015 opdateret af: Children's Hospital of Philadelphia
Using Health Information Technology to Improve Healthcare Quality in Primary Care Practices and in Transitions Between Care Settings
This study will test the effectiveness of clinician-focused health IT-based decision support, family-focused health IT-based decision support, and a combination of both efforts, in increasing HPV and other adolescent vaccine rates among adolescent girls.
We hypothesize that a combination of clinician-focused clinical decision support and family-focused decision support will be most effective.
Studieoversigt
Status
Afsluttet
Betingelser
Detaljeret beskrivelse
- Clinician-focused intervention includes an electronic health record-based decision support mechanism including reminders, education, audit and feedback on vaccination success.
- Family-focused intervention includes vaccine reminders and informational telephone calls prompted by the electronic health record.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
23675
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Pennsylvania
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Philadelphia, Pennsylvania, Forenede Stater, 19103
- Children's Hospital of Philadelphia
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-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
11 år til 17 år (Barn)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Kvinde
Beskrivelse
Inclusion Criteria:
- All clinicians practicing at participating sites
- Parents with an eligible adolescent girl
- Adolescent girls
- Ages 11-17
- Has a visit at one of the primary care centers within the last 15 months.
- Has not completed the teen vaccine series
Exclusion Criteria:
- None
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Sundhedstjenesteforskning
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Family Decision Support
Families will receive informational vaccine reminder telephone calls.
|
Family-focused intervention includes informational vaccine reminder telephone calls prompted by an electronic health record.
Andre navne:
|
|
Eksperimentel: Clinical Decision Support
In this treatment arm, clinicians receive the decision support at the point of care within an electronic health record.
|
Clinician-focused intervention includes an electronic health record-based decision support mechanism including reminders, education, audit and feedback on vaccination success.
Andre navne:
|
|
Eksperimentel: Family DS+ Clinician DS
Families will receive informational vaccine reminder calls and their clinicians will receive electronic health record-based decision support for immunizations.
|
Family-focused intervention includes informational vaccine reminder telephone calls prompted by an electronic health record.
Andre navne:
Clinician-focused intervention includes an electronic health record-based decision support mechanism including reminders, education, audit and feedback on vaccination success.
Andre navne:
This will be a combination of the family-focused decision support (telephone reminder calls) and clinician-focused decision support (clinical alerts).
Andre navne:
|
|
Andet: Control
This group will receive regular primary care with no decision support.
|
Sædvanlig pleje
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Rate of HPV vaccination among girls actively cared for at participating sites
Tidsramme: Monthly, up to 1 year
|
The outcome will be assessed monthly, until study completion (1 year).
|
Monthly, up to 1 year
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Rates of meningococcal and tetanus, diphtheria, and pertussis vaccines among girls in the study
Tidsramme: Monthly, up to 1 year
|
The outcome will be assessed monthly, until study completion (1 year).
|
Monthly, up to 1 year
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Alexander G Fiks, MD, MSCE, Children's Hospital of Philadelphia
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. maj 2010
Primær færdiggørelse (Faktiske)
1. maj 2011
Studieafslutning (Faktiske)
1. maj 2011
Datoer for studieregistrering
Først indsendt
7. juli 2010
Først indsendt, der opfyldte QC-kriterier
7. juli 2010
Først opslået (Skøn)
9. juli 2010
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
12. marts 2015
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
11. marts 2015
Sidst verificeret
1. august 2011
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- 09-00-7352
- AHRQ (Andet bevillings-/finansieringsnummer: 1R01HS029874-01A1)
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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