search
Back to results

The INFLUENTIAL Trial- Evaluation of National Inpatient Influenza Vaccination Program (Influential)

Primary Purpose

Influenza

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Existing Influenza Vaccination Practices
Standardized inpatient influenza vaccination program
Sponsored by
University of Colorado, Denver
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Influenza focused on measuring vaccination, influenza

Eligibility Criteria

6 Months - 99 Years (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: At least 6 months of age Admitted to an inpatient unit at a participating health system Exclusion: - Admission to critical care sites or hematology-oncology services Exclusion Criteria: At least 6 months of age Admitted to an inpatient unit at a participating health system Exclusion: - Admission to critical care sites or hematology-oncology services

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    Standardized inpatient influenza vaccination program

    Existing inpatient influenza vaccination practices

    Arm Description

    Intervention A: The basic intervention is the inpatient influenza vaccination program, which will be comprised of the following core components: informatics and data analytic tools, evidenced-based education and communication, a multidisciplinary leadership team, and end-user engagement. Intervention B: The intensified intervention is the multifaceted influenza vaccination strategy (Intervention A) plus a learning collaborative with lead site facilitation during the trial period.

    Usual care is defined as the inpatient influenza vaccination practices that currently exist at a given site.

    Outcomes

    Primary Outcome Measures

    Vaccine administration rate
    proportion of influenza vaccine administrations to eligible patients during hospitalization.

    Secondary Outcome Measures

    Full Information

    First Posted
    April 9, 2023
    Last Updated
    August 28, 2023
    Sponsor
    University of Colorado, Denver
    Collaborators
    Agency for Healthcare Research and Quality (AHRQ), Seattle Children's Hospital
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT05832307
    Brief Title
    The INFLUENTIAL Trial- Evaluation of National Inpatient Influenza Vaccination Program
    Acronym
    Influential
    Official Title
    The INFLUENTIAL Trial - Inpatient FLU Vaccination Program Effectiveness: National Trial Implementing Best Practices and Learning Collaboratives
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 17, 2023 (Anticipated)
    Primary Completion Date
    July 31, 2027 (Anticipated)
    Study Completion Date
    July 31, 2027 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of Colorado, Denver
    Collaborators
    Agency for Healthcare Research and Quality (AHRQ), Seattle Children's Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    This study plans to learn more about whether a stakeholder-informed, standardized inpatient vaccination program will increase influenza vaccination rates of hospitalized children across US pediatric health systems. The first part of the study is to form a multidisciplinary team of stakeholders, including parents, providers, nurses, pharmacists, informaticists, data analysts and communication experts across three sites in synthesizing a best practice implementation guide for an inpatient influenza vaccination program, which will then be piloted at these three sites.
    Detailed Description
    The overarching goal of this proposal is to determine whether a stakeholder-informed, standardized inpatient influenza vaccination program will increase influenza vaccination rates of hospitalized children across diverse U.S. pediatric health systems. Building upon preliminary data and experience with pediatric inpatient influenza vaccine delivery, the investigators will engage a multidisciplinary team of stakeholders in synthesizing a best practice implementation guide for an inpatient influenza vaccination program across three sites. The next phase of the study, using a novel adaptive trial design, will be to implement and test the program across 12 health systems. Finally, the investigators will evaluate the program's impact using an established dissemination and implementation framework.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Influenza
    Keywords
    vaccination, influenza

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Not Applicable
    Interventional Study Model
    Sequential Assignment
    Model Description
    The investigators will conduct a cluster SMART to evaluate the effectiveness of an inpatient influenza vaccination program on influenza vaccination rates during hospitalization at 12 U.S. pediatric health systems over 3 influenza vaccination seasons (Study Years 3-5). Sites will be randomized to the standardized influenza vaccination program or usual care in the first intervention season (traditional cluster RCT). Usual care and low performing sites will be re-randomized to the standardized program (intervention A) or the standardized program with an intensified implementation strategy (intervention B) in the second season. Sites will continue their programs in the third season to assess sustainability. The unit of intervention (randomization) is the site (i.e., health system).
    Masking
    None (Open Label)
    Masking Description
    Sites will be randomized 2:1 by the study statistician to intervention A vs. usual care. The randomization will be stratified by academic or academic plus community setting. This will ensure that the groups are balanced for site variables that may be correlated with the outcomes of interest. After the first intervention season, the 4 usual care sites and 6 lowest performing intervention sites (lowest change in vaccination rates from their baseline data) will be randomized 1:1 to intervention A vs. intervention B.
    Allocation
    Randomized
    Enrollment
    22000 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Standardized inpatient influenza vaccination program
    Arm Type
    Active Comparator
    Arm Description
    Intervention A: The basic intervention is the inpatient influenza vaccination program, which will be comprised of the following core components: informatics and data analytic tools, evidenced-based education and communication, a multidisciplinary leadership team, and end-user engagement. Intervention B: The intensified intervention is the multifaceted influenza vaccination strategy (Intervention A) plus a learning collaborative with lead site facilitation during the trial period.
    Arm Title
    Existing inpatient influenza vaccination practices
    Arm Type
    Active Comparator
    Arm Description
    Usual care is defined as the inpatient influenza vaccination practices that currently exist at a given site.
    Intervention Type
    Other
    Intervention Name(s)
    Existing Influenza Vaccination Practices
    Intervention Description
    Usual care is defined as the existing inpatient influenza vaccination practices that currently exist at a given site.
    Intervention Type
    Other
    Intervention Name(s)
    Standardized inpatient influenza vaccination program
    Other Intervention Name(s)
    Intervention A and B
    Intervention Description
    Intervention A: The basic intervention is the inpatient influenza vaccination program Intervention B: The intensified intervention is the multifaceted influenza vaccination strategy (Intervention A) plus a learning collaborative
    Primary Outcome Measure Information:
    Title
    Vaccine administration rate
    Description
    proportion of influenza vaccine administrations to eligible patients during hospitalization.
    Time Frame
    1 year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    6 Months
    Maximum Age & Unit of Time
    99 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: At least 6 months of age Admitted to an inpatient unit at a participating health system Exclusion: - Admission to critical care sites or hematology-oncology services Exclusion Criteria: At least 6 months of age Admitted to an inpatient unit at a participating health system Exclusion: - Admission to critical care sites or hematology-oncology services
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Suchitra Rao
    Phone
    7207772823
    Email
    suchitra.rao@childrenscolorado.org
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Suchitra Rao
    Organizational Affiliation
    University of Colorado, Children's Hospital Colorado
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    The INFLUENTIAL Trial- Evaluation of National Inpatient Influenza Vaccination Program

    We'll reach out to this number within 24 hrs