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Using Rapid Cycle Randomized Controlled Trials to Optimize the Influenza Clinical Decision Support Tool

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ClinicalTrials.gov Identifier: NCT03415425
Recruitment Status : Recruiting
First Posted : January 30, 2018
Last Update Posted : January 30, 2018
Sponsor:
Information provided by (Responsible Party):
New York University School of Medicine

Brief Summary:
The proposed study aims to examine several iterations of the Influenza Best Practice Alert at NYU Langone Health. The goal is to increase ordering of the influenza vaccine through the alert.

Condition or disease Intervention/treatment Phase
Clinical Decision Support Other: Current Version of the Influenza Alert Other: Alternate Modifications of the Influenza Alert Not Applicable

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 4000 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
Official Title: Using Rapid Cycle Randomized Controlled Trials to Optimize the Influenza Clinical Decision Support Tool
Actual Study Start Date : January 16, 2018
Estimated Primary Completion Date : January 16, 2019
Estimated Study Completion Date : April 30, 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Flu Flu Shot

Arm Intervention/treatment
Active Comparator: Usual Care
The current version of the alert will fire for this arm of the study.
Other: Current Version of the Influenza Alert
Intervention includes the current version of the Influenza Alert that fires in the electronic medical record if the patient has not received the flu vaccination, as part of usual care.

Active Comparator: Alert Iteration
A modified version of the alert will fire for this arm of the study.
Other: Alternate Modifications of the Influenza Alert
Intervention includes various iterations of the Influenza Alert that fires in the electronic medical record if the patient has not received the flu vaccination.




Primary Outcome Measures :
  1. Alert Cancelation Rate [ Time Frame: 2 months. ]
    Number of times alert fires in medical record within 2 Month period


Secondary Outcome Measures :
  1. Vaccination Rate at Discharge [ Time Frame: 2 months ]
    Number of vaccinations recorded in EMR within 2 Month period



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Ages Eligible for Study:   3 Years and older   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • All NYU Langone Health inpatients eligible for the Influenza clinical decision support tool

Exclusion Criteria:


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03415425


Contacts
Contact: Masha Kuznetsova, MPH 6465012919 masha.kuznetsova@nyumc.org

Locations
United States, New York
New York University School of Medicine Recruiting
New York, New York, United States, 10016
Contact: Masha Kuznetsova    646-501-2919    Masha.Kuznetsova@nyumc.org   
Principal Investigator: Leora Horwitz, MD, MHS         
Sponsors and Collaborators
New York University School of Medicine
Investigators
Principal Investigator: Leora Horwitz, MD, MHS New York University School of Medicine

Responsible Party: New York University School of Medicine
ClinicalTrials.gov Identifier: NCT03415425     History of Changes
Other Study ID Numbers: RCT CDS
First Posted: January 30, 2018    Key Record Dates
Last Update Posted: January 30, 2018
Last Verified: January 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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