Using Rapid Cycle Randomized Controlled Trials to Optimize the Influenza Clinical Decision Support Tool
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT03415425|
Recruitment Status : Recruiting
First Posted : January 30, 2018
Last Update Posted : January 30, 2018
|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|
|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|
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.
- Alert Cancelation Rate [ Time Frame: 2 months. ]Number of times alert fires in medical record within 2 Month period
- Vaccination Rate at Discharge [ Time Frame: 2 months ]Number of vaccinations recorded in EMR within 2 Month period
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
|Contact: Masha Kuznetsova, MPHfirstname.lastname@example.org|
|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|
|Principal Investigator:||Leora Horwitz, MD, MHS||New York University School of Medicine|