Testing a Provider-Level Feedback Intervention to Optimize Postoperative Prescribing
NCT ID: NCT04776928
Last Updated: 2023-11-21
Study Results
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View full resultsBasic Information
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COMPLETED
NA
217 participants
INTERVENTIONAL
2022-03-17
2022-08-17
Brief Summary
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The study is being completed to learn more about the effectiveness, feasibility, and acceptability and that the goal is both to evaluate how effective this intervention and mechanism are for changing surgeon opioid prescribing behavior and to inform best practices for future quality initiatives. The study hypothesizes that provider-level feedback will allow clinicians to tailor postoperative prescribing more closely to patient consumption, and reduce excess postoperative prescribing.
The cohort of surgeons which have been identified as outliers by the Michigan Surgical Quality Collaborative (MSQC) will be be invited to participate in this trial. The study team will send surgeons belonging to sites that signed the Exhibit B-1 form the provider-level push notifications (98 participants). In this study de-identified prescribing data will also be analyzed for sites that do not sign the Exhibit B-1 form (105 participants).
The study team will approach 98 surgeons receiving the provider-level push notifications in one wave.
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
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Provider-level push report notifications
Push reports will be sent via using a secure email client. The email will be sent to the email address provided to the study team by the surgeon or site.
Push reports
Surgeons in the experimental arm will receive provider-level push report notifications through an email displaying their personal prescribing performance compared to Michigan Opioid Prescribing Engagement Network (OPEN) prescribing guidelines and their de-identified peers.
The push report will also include a link to the secure MSQC data platform that displays more information about the case so the surgeon can further investigate prescribing information. The email will also contain contact information for the study team so as to help any surgeons troubleshoot, learn more, request to stop receiving reports, etc.
No intervention
Sites who did not sign Exhibit B-1.
No interventions assigned to this group
Interventions
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Push reports
Surgeons in the experimental arm will receive provider-level push report notifications through an email displaying their personal prescribing performance compared to Michigan Opioid Prescribing Engagement Network (OPEN) prescribing guidelines and their de-identified peers.
The push report will also include a link to the secure MSQC data platform that displays more information about the case so the surgeon can further investigate prescribing information. The email will also contain contact information for the study team so as to help any surgeons troubleshoot, learn more, request to stop receiving reports, etc.
Eligibility Criteria
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Inclusion Criteria
* Surgeons within MSQC who have median prescribing \> 1 pill equivalents over the published recommendation
* Surgeons within MSQC who perform surgeries at a hospital that have agreed to participate in this research
Exclusion Criteria
18 Years
ALL
No
Sponsors
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National Institute on Drug Abuse (NIDA)
NIH
University of Michigan
OTHER
Responsible Party
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Jennifer Waljee
Associate Professor of Surgery and Associate Professor of Orthopaedic Surgery
Principal Investigators
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Jennifer F Waljee, MD
Role: PRINCIPAL_INVESTIGATOR
University of Michigan
Locations
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University of Michigan
Ann Arbor, Michigan, United States
Countries
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Provided Documents
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Document Type: Study Protocol
Other Identifiers
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HUM00186352
Identifier Type: -
Identifier Source: org_study_id
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