Centralized IIS-based Reminder/Recall to Increase Childhood Influenza Vaccination Rates_2nd Trial in Colorado
Primary Purpose
Reminder Systems, Influenza Vaccines
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Reminders
Sponsored by
About this trial
This is an interventional health services research trial for Reminder Systems focused on measuring centralized reminder/recall, influenza vaccine reminders, childhood influenza vaccines
Eligibility Criteria
Inclusion Criteria:
- have record in Colorado Immunization Information System
- from 6 months through 17 years of age
- have not received an influenza vaccine by start of trial
- must be affiliated with one of our 42 randomly selected primary care practices in Colorado
Exclusion Criteria:
- those without a record
- received an influenza vaccine post 9/1/2017
- not affiliated with an eligible study
Sites / Locations
- University of Colorado
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
No Intervention
Experimental
Experimental
Arm Label
Control
Autodialer R/R
Mail R/R
Arm Description
These patients will receive no reminders from the health department and will receive usual care.
Autodialer calls (up to 3 reminders)- with brief education message + practice name + practice phone #
Mailed reminder (up to 3 reminders)-- with brief education message + practice name + practice phone #
Outcomes
Primary Outcome Measures
Receipt of at least 1 influenza vaccine according to immunization records in the Immunization Information System (IIS) records in each state
Based on our prior studies, we currently plan to send up to 3 autodialer or postcards (based on randomization arm) reminders, spaced every 5 weeks, beginning in early October, and ending mid-December 2017. Outcomes are assessed at 6 months using IIS data.
Secondary Outcome Measures
Full Information
NCT ID
NCT03246100
First Posted
August 7, 2017
Last Updated
June 20, 2019
Sponsor
University of Colorado, Denver
Collaborators
University of California, Los Angeles
1. Study Identification
Unique Protocol Identification Number
NCT03246100
Brief Title
Centralized IIS-based Reminder/Recall to Increase Childhood Influenza Vaccination Rates_2nd Trial in Colorado
Official Title
Centralized IIS-based Reminder/Recall to Increase Childhood Influenza Vaccination Rates, 2nd Trial in Colorado
Study Type
Interventional
2. Study Status
Record Verification Date
June 2019
Overall Recruitment Status
Completed
Study Start Date
September 6, 2017 (Actual)
Primary Completion Date
April 30, 2019 (Actual)
Study Completion Date
April 30, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Colorado, Denver
Collaborators
University of California, Los Angeles
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study is the second trial related to ClinicalTrials.gov ID: NCT02761551. There are slight changes to methods and a different cohort will be used, thus justifying a 2nd ClinicalTrials.gov submission. This trial is taking place in New York State (not NYC) and in Colorado. Each state has it's own ClinicalTrials.gov submission.
Despite U.S. guidelines for influenza vaccination of all children starting at age 6 months, only about half of children are vaccinated annually leading to substantial influenza disease in children and spread of disease to adults. A major barrier is that families are not reminded about the need for their children to receive influenza vaccination. The investigators will evaluate the impact of patient reminder/recall (R/R) performed by state immunization information systems to improve influenza vaccination rates by using three clinical trials in two states. The investigators will assess effectiveness and cost-effectiveness of: 1) autodialer reminder/recall versus 2) postcard reminder/recall versus 3) usual care (no R/R) on improving influenza vaccination rates.
The investigators will disseminate the state immunization information system based reminder/recall system to all states for use for both seasonal and pandemic influenza vaccinations with the goal of lowering influenza morbidity.
Detailed Description
Annual epidemics of seasonal influenza cause substantial morbidity and mortality in the U.S. with high rates of hospitalizations, emergency department and outpatient visits, and medical costs. Children experience significant morbidity from influenza, and also play a critical role in spreading infection to adults. Since 2010, the Advisory Committee on Immunization Practices (ACIP) has recommended influenza vaccination for all children >6 months of age. However, vaccination rates remain very low-- only 56% of children 2-17 years are vaccinated. Low rates are a concern for both seasonal influenza and in preparation for pandemic influenza. One of the nationally recommended strategies for raising childhood influenza vaccination rates is to use parent reminder/recall (R/R) by phone or mail, which can raise rates by up to 20 percentage points. However, less than 16% of primary care practices use R/R despite many studies showing its effectiveness.
Statewide immunization information systems (IISs) now exist in all states to track childhood vaccinations, but they have not been used for R/R for influenza vaccine because of the lack of evidence for its effectiveness and lack of a template for IIS-based R/R. The investigators have united two leading immunization research groups (Denver, CO and Rochester, NY) to assess the impact of centralized IIS-based influenza vaccine R/R, and to evaluate the effect of two types of R/R (autodial v. mail R/R) over usual care. The investigators will also develop tools to aid other states in creating efficient IIS R/R systems for seasonal and possible pandemic influenza outbreaks.
In Colorado, evaluate the impact of (a) autodialer reminders and (b) mailed messages versus standard-of-care control on raising influenza vaccination rates among children 6m-17 years of age.
The investigators propose a 3-arm RCT study design with the following study arms:
Standard of care control
Autodialer (3 reminders)- with brief education message + practice name + practice phone #
Mailed reminder (3 reminders)-- with brief education message + practice name + practice phone #
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Reminder Systems, Influenza Vaccines
Keywords
centralized reminder/recall, influenza vaccine reminders, childhood influenza vaccines
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients will be randomized within practices to one of 3 arms:
Standard of care control
Autodialer (3 reminders)- with brief education message + practice name + practice phone # (see autodialer scripts)
Mailed reminder (3 reminders)-- with brief education message + practice name + practice phone # (see postcards)
Masking
Participant
Allocation
Randomized
Enrollment
25531 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control
Arm Type
No Intervention
Arm Description
These patients will receive no reminders from the health department and will receive usual care.
Arm Title
Autodialer R/R
Arm Type
Experimental
Arm Description
Autodialer calls (up to 3 reminders)- with brief education message + practice name + practice phone #
Arm Title
Mail R/R
Arm Type
Experimental
Arm Description
Mailed reminder (up to 3 reminders)-- with brief education message + practice name + practice phone #
Intervention Type
Behavioral
Intervention Name(s)
Reminders
Intervention Description
Reminders are sent either through autodial or postcards reminding patients to get flu vaccine.
Primary Outcome Measure Information:
Title
Receipt of at least 1 influenza vaccine according to immunization records in the Immunization Information System (IIS) records in each state
Description
Based on our prior studies, we currently plan to send up to 3 autodialer or postcards (based on randomization arm) reminders, spaced every 5 weeks, beginning in early October, and ending mid-December 2017. Outcomes are assessed at 6 months using IIS data.
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
have record in Colorado Immunization Information System
from 6 months through 17 years of age
have not received an influenza vaccine by start of trial
must be affiliated with one of our 42 randomly selected primary care practices in Colorado
Exclusion Criteria:
those without a record
received an influenza vaccine post 9/1/2017
not affiliated with an eligible study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Allison Kempe, MD, MPH
Organizational Affiliation
University of Colorado, Denver
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Colorado
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Aggregate results will be prepared for publications at the end of the trial.
Citations:
PubMed Identifier
32446470
Citation
Szilagyi PG, Albertin CS, Saville AW, Valderrama R, Breck A, Helmkamp L, Zhou X, Vangala S, Dickinson LM, Tseng CH, Campbell JD, Whittington MD, Roth H, Rand CM, Humiston SG, Hoefer D, Kempe A. Effect of State Immunization Information System Based Reminder/Recall for Influenza Vaccinations: A Randomized Trial of Autodialer, Text, and Mailed Messages. J Pediatr. 2020 Jun;221:123-131.e4. doi: 10.1016/j.jpeds.2020.02.020.
Results Reference
derived
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Centralized IIS-based Reminder/Recall to Increase Childhood Influenza Vaccination Rates_2nd Trial in Colorado
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