Optimizing Application And Support Of Immunization Information Systems (OASIS)

University of Rochester

Status: Completed

Conditions: Increase in HPV Vaccination Rate; Increase in Use of Immunization Registry

Treatments: Other: Audit-Feedback/Immunization Forecasting Reports; Other: Reminder Recall Report

Study type: Interventional

Funder types: Other; Other U.S. Federal agency

Identifiers

NCT02010372

5U01IP000502

Details and patient eligibility

About

The overall purpose of this study is to evaluate the use of features of the New York State Immunization Information System (NYSIIS) by various types of primary care practices and determine how best to promote the use of IIS features and functionality. The primary goal is to promote the use of NYSIIS for immunization quality improvement (QI) in the practice setting. Customized training sessions will be conducted by study staff to educate practices on NYSIIS' enhanced features.

Enrollment: 31 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• NYSIIS administrator at a participating practice

Exclusion criteria

• Practices already utilizing/running reports used in the intervention

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Factorial Assignment

Masking: None (Open label)

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31 participants in 3 patient groups

Reminder Recall Reports

Experimental group

Description:

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.

Treatment:

Other: Reminder Recall Report

Audit-Feedback/Immunization Forecasting Reports

Experimental group

Description:

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.

Treatment:

Other: Audit-Feedback/Immunization Forecasting Reports

Control

No Intervention group

Description:

No intervention will be administered to this group.