Optimizing Application And Support Of Immunization Information Systems (OASIS) (OASIS)
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|ClinicalTrials.gov Identifier: NCT02010372|
Recruitment Status : Completed
First Posted : December 12, 2013
Last Update Posted : February 25, 2016
|Condition or disease||Intervention/treatment||Phase|
|Increase in Use of Immunization Registry Increase in HPV Vaccination Rate||Other: Reminder Recall Report Other: Audit-Feedback/Immunization Forecasting Reports||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||31 participants|
|Intervention Model:||Factorial Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Health Services Research|
|Official Title:||Optimizing the Practical Application of Immunization Information System Use in Primary Care Practices|
|Study Start Date :||December 2013|
|Actual Primary Completion Date :||May 2015|
|Actual Study Completion Date :||July 2015|
Experimental: Reminder Recall Reports
Training in how to use reminder-recall reports in the Immunization registry will be given to administrators who will then be asked to regularly run these reports for a period of one year.
Other: Reminder Recall Report
Practices (administrators) that are randomized to this intervention will receive training in how to run reminder recall reports for patients due to receive any dose of HPV vaccine. After the training has been completed, administrators will be asked to continue running regularly scheduled reports over the course of one year. A tracking log will be sent regularly to the research team.
Experimental: Audit-Feedback/Immunization Forecasting Reports
Training in how to use audit-feedback/immunization forecasting reports in the Immunization registry will be given to administrators who will then be asked to regularly run these reports for a period of one year.
Other: Audit-Feedback/Immunization Forecasting Reports
Practices (administrators) that are randomized to this intervention will receive training in how to run audit-feedback/immunization forecasting reports for patients due to receive any dose of HPV vaccine and to determine the % of patients in their practice who have received at least one dose of HPV vaccine within the study period. After the training has been completed, administrators will be asked to continue running regularly scheduled reports over the course of one year. A tracking log will be sent regularly to the research team.
No Intervention: Control
No intervention will be administered to this group.
- NYSIIS report usage [ Time Frame: One Year ]Practice NYSIIS administrators will monitor the number of reports their practice generates throughout the 12 month post-training period. These measures for control and intervention practices will be compared in bivariate and multivariate analysis.
- HPV Vaccination Rate [ Time Frame: One Year ]HPV Vaccination rates will be measured to determine the change in the practice's immunization levels (for the pre-determined immunization QI goal) over the 12-month period following their initial training. Statistical comparisons of control and intervention practice will be performed using bivariate analyses, while multivariate analyses will be used to account for the effects of practice characteristics.
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): NCT02010372
|United States, New York|
|University of Rochester|
|Rochester, New York, United States, 14642|
|Principal Investigator:||Stanley J Schaffer, MD, MPH||University of Rochester|