- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01146899
FluAlert: Influenza Vaccine Alerts for Providers in the Electronic Health Record
June 22, 2014 updated by: Melissa Stockwell, MD, MPH, Columbia University
Childhood influenza coverage rates are far below rates for the other childhood vaccinations.
Increasing influenza vaccine coverage rates is important not only for the health of the child, but for that of the child's household and community.
Yet,influenza vaccine delivery rates at pediatric clinics are low, even when the vaccine is available.
The proposed project will take advantage of existing health information technology to tailor, implement and evaluate influenza vaccine alerts in the electronic health record (EHR) for pediatric providers to help improve health care decision making.
Study Overview
Study Type
Interventional
Enrollment (Actual)
6145
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
-
-
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
6 months to 75 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Medical (medical doctor/nurse practitioner (MD/NP)) or nursing providers (registered nurse, licensed practical nurse (RN/LPN)) at participating practices
- Parents of a child 6 months - 18 years who is a patient at one of the participating ACN practice
- Parents fluent in English or Spanish
- Children 6 months- 18 years with visit to participating practice during influenza season
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 Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Provider Alert
Provider receives alert for patient visit
|
Provider influenza vaccine alert
Other Names:
|
No Intervention: No Alert
No alert provided
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
influenza vaccination
Time Frame: September through March 2011-2012
|
September through March 2011-2012
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Documentation of reason for vaccine refusal
Time Frame: Sept 2011-March 2012
|
Sept 2011-March 2012
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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
December 1, 2009
Primary Completion (Actual)
March 1, 2013
Study Completion (Actual)
June 1, 2013
Study Registration Dates
First Submitted
June 16, 2010
First Submitted That Met QC Criteria
June 16, 2010
First Posted (Estimate)
June 22, 2010
Study Record Updates
Last Update Posted (Estimate)
June 24, 2014
Last Update Submitted That Met QC Criteria
June 22, 2014
Last Verified
June 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AAAE4956
- 1R18HS018158-01 (U.S. AHRQ Grant/Contract)
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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