Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02010372 · ClinicalTrials.gov registry record · NA
Optimizing Application And Support Of Immunization Information Systems (OASIS)
A NA study of Increase in Use of Immunization Registry and Increase in HPV Vaccination Rate, sponsored by University of Rochester.
- Completed
- Registry status
- NA
- Development phase
- 31
- Enrollment target
- 1
- Study location
NCT02010372: Completed NA study of Increase in Use of Immunization Registry and Increase in HPV Vaccination Rate, sponsored by University of Rochester.
NCT02010372 is a NA study of Increase in Use of Immunization Registry and Increase in HPV Vaccination Rate that has completed, run by University of Rochester. The registered enrollment target is 31 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02010372, a NA study of Increase in Use of Immunization Registry and Increase in HPV Vaccination Rate, has completed, sponsored by University of Rochester.
- COMPLETED
- Registry status
- NA
- Development phase
- 31 participants
- Enrollment target
- 1
- Study location
Study Summary
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.
Primary Outcome
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.
Conditions Studied
Interventions
- OTHER Reminder Recall Report
- OTHER Audit-Feedback/Immunization Forecasting Reports
Study Locations (1)
New York
- University of Rochester - Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 31 participants |
| Start Date | 2013-12 |
| Est. Completion | 2015-07 |
| Phase | NA |
What the finished NCT02010372 record still lists
NCT02010372 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).
The record links to 2 conditions, with Increase in Use of Immunization Registry appearing as the primary indexed condition, and to 2 interventions - of which Reminder Recall Report is the first listed.
NCT02010372 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT02010372 about?
NCT02010372 is a clinical study titled "Optimizing Application And Support Of Immunization Information Systems (OASIS)". 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...
What is the current status of trial NCT02010372?
This trial is currently completed. It is a NA study. The enrollment target is 31 participants. The study started on 2013-12. Estimated completion is 2015-07.
What conditions does trial NCT02010372 study?
This clinical trial studies the following conditions: Increase in Use of Immunization Registry, Increase in HPV Vaccination Rate.
What interventions are being tested in trial NCT02010372?
The interventions under investigation include: Reminder Recall Report (OTHER), Audit-Feedback/Immunization Forecasting Reports (OTHER).
Who is sponsoring clinical trial NCT02010372?
This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02010372 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02010372's enrollment target sits among peer trials
31 1592nd of 2000 higher than 408 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT02932618 · 31 participants · Phase 3
A Study of Recombinant Von Willebrand Factor (rVWF) With or Without ADVATE in Children With Severe Von Willebrand Disease (VWD)
- NCT03482297 · 31 participants · Phase 1
Automated Abdominal Binder for Orthostatic Hypotension
- NCT04016389 · 31 participants · NA
FIGO 2018 Stage IB2 Cervical Cancer Treated With Neoadjuvant Chemotherapy Followed by Fertility Sparing Surgery
- NCT04211675 · 31 participants · Phase 1
NK Cells Infusions With Irinotecan, Temozolomide, and Dinutuximab
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia