Synchronized Immunization NotifiCations (SINC)

September 3, 2019 updated by: Melissa Stockwell, Columbia University

Immunization is one of the most effective public health interventions. Yet, nationally coverage has consistently fallen short of national goals, and has remained for the most part stagnant. The continued presence of vaccine-preventable diseases poses a threat to public health. In addition to needed improvement of immunization coverage for the general pediatric/adolescent population, some children with chronic medical conditions need specific additional immunizations, yet many fail to receive them.

Immunization reminders for providers in the electronic health record (EHR) are a type of clinical decision support (CDS) that can reduce missed immunization opportunities. One limitation of these reminders is that they generally depend only on data local to the EHR, which can be incomplete due to record scatter, leading to inaccurate alerts. An Immunization Information System (IIS), also known as an immunization registry, is a population-based system that collects immunization data primarily for children and adolescents from providers at a regional or state level.

The investigators seek to couple bidirectional exchange of IIS immunization information and forecasting tools with patient level medical history from the EHR to deliver accurate, patient-specific EHR immunization reminders.

Study Overview

Status

Completed

Conditions

Detailed Description

National immunization coverage has consistently fallen short of Healthy People 2010 and 2020 goals and has remained relatively stagnant over the past few years for many immunizations. One important group with a high risk of under-immunization are children with chronic medical conditions (CMCs), who are also at increased risk of serious morbidity and even death from vaccine preventable diseases. One of the key interventions to improve immunization coverage in both the general population and children with CMCs is to decrease missed opportunities for immunization. Immunization reminders in the electronic health record (EHR) are a type of clinical decision support (CDS) that can reduce missed opportunities. In a recent project, the investigators successfully employed such reminders to increase influenza immunization.

One limitation of EHR immunization reminders is that they generally act only on local EHR immunization data. If that data is incomplete, a provider may be erroneously alerted to order an immunization the child does not need. The likelihood of incomplete local data is high. Nearly one-quarter of children in the U.S. visit more than one immunization provider in their first three years of life, leading to fragmented and incomplete records. Low-income and minority children are especially susceptible to immunization record fragmentation as they are more likely to receive care from multiple clinics and providers. Children with CMCs are also at high-risk since their care is often shared between a primary care provider and subspecialists.Harnessing Immunization Information Systems (IIS) data can help overcome this limitation. IIS are population-based systems that collect immunization data primarily for children and adolescents from providers at a regional or state level, consolidating patient's immunization data into a single location no matter where administered. There are currently IIS in 50 states, five cities, and the District of Columbia. However, in most cases, IIS data are available to providers only on the IIS's website. Yet, frontline care providers are most likely to benefit when an IIS provides information at point of patient care within their EHR workflow. This type of bidirectional exchange of immunization information between IIS and EHR systems is a proposed Stage 3 Meaningful Use objective; this consolidated data would be the most complete data to use for an EHR reminder, but is rarely used.

Another challenge associated with EHR-based immunization reminders is that pediatric and adolescent immunization schedules are complex, requiring up to 35 immunizations plus the annual influenza vaccine. Each immunization series has its own minimum age and dosing intervals, and new immunizations are not uncommon. However, many EHRs may not have or aggressively maintain comprehensive immunization decision rules.

IIS can help overcome this limitation as well. Many include tools for forecasting when doses are next due and can provide that information during data exchange with an EHR, but that has not been assessed.

Bringing IIS immunization data and forecasting tools into a local EHR to power CDS will be helpful for the general population. However, one limitation of immunization CDS, whether provided by an IIS or native to the EHR, is that it does not account for subtleties required by children with certain CMCs who may need extra immunizations specific to their condition or cannot receive certain immunizations. A logical next-step is to couple exchange of IIS immunization data and forecasting tools with patient-level EHR information regarding medical conditions to power accurate, patient-specific EHR immunization reminders. This has yet to be done.

Aim 1: Assess the impact of EHR reminders integrated with immunization data and forecasting from a regional IIS on receipt of generally recommended immunizations in a low-income, urban, pediatric and adolescent population.

Aim 2: Assess the impact of integrated EHR reminders that also incorporate patient's medical conditions on receipt of immunizations specifically recommended for children and adolescents with chronic medical conditions.

Hypothesis 1: Lower rates of under-immunization will be observed when reminders are 'on' vs. 'off'.

Hypothesis 2: Lower rates of over-immunization will be observed when reminders are 'on' vs. 'off'.

Hypothesis 3: Higher rates of captured opportunities will be observed when reminders are 'on' vs. 'off'.

Hypothesis 4: There will be no difference in reminder impact on generally recommended immunizations for children with and without chronic medical conditions (CMCs)

In this three-year project, investigators will conduct a randomized cluster crossover pragmatic clinical trial to assess immunization outcomes during periods when an integrated immunization reminder is 'on' vs. 'off' for generally recommended immunizations as well as ones specific for children with CMCs. The proposed work will generate empiric knowledge regarding the best practices for implementing IIS-supported immunization reminders for both children with and without CMCs. The results may help guide local and national efforts on both immunization data exchange and EHR reminders.

Study Type

Interventional

Enrollment (Actual)

15348

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

    • New York
      • New York, New York, United States, 10032
        • Columbia University Medical Center/ NewYork Presbyterian Hospital Ambulatory Care Network
    • Washington
      • Seattle, Washington, United States, 98101
        • Seattle Children's Research Institute

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

No older than 17 years (CHILD)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • medical visit at study site during analytic period

Exclusion Criteria:

  • none

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: CROSSOVER
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Immunization Alert on
Children with visits seen when the immunization alert is on
Immunization alert in the electronic health record
NO_INTERVENTION: Immunization Alert off
Children with visits seen when the alert is off

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Under-immunization- general recommendations
Time Frame: 1 day
Percent of children and adolescents seen during the study periods who are overdue for at least one age appropriate immunization as recommended by the CDC's Advisory Committee on Immunization Practices
1 day
Under-immunization- recommendations for children with chronic medical conditions
Time Frame: 1 day
Percent of children and adolescents with a chronic medical condition for which a specific additional immunization is recommended who are seen during the study periods who are overdue for at least one of these specific immunizations
1 day
Over-immunization
Time Frame: 1 day
Percent of children who have received at least one immunization in excess of the recommended immunizations for their age or condition
1 day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Captured opportunity
Time Frame: 1 day
Proportion of medical visits in the analytic period during which a child/adolescent was eligible for an immunization, and received it
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

June 6, 2017

Primary Completion (ACTUAL)

June 5, 2018

Study Completion (ACTUAL)

June 5, 2018

Study Registration Dates

First Submitted

March 12, 2016

First Submitted That Met QC Criteria

March 12, 2016

First Posted (ESTIMATE)

March 16, 2016

Study Record Updates

Last Update Posted (ACTUAL)

September 6, 2019

Last Update Submitted That Met QC Criteria

September 3, 2019

Last Verified

September 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • AAAP6516
  • 5R01HS023582-03 (AHRQ)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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.

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