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Clinical Trials/NCT03825549
NCT03825549
Completed
Not Applicable

A Randomized Trial of Behavioral Economic Approaches to Reduce Unnecessary Opioid Prescribing

University of Pennsylvania1 site in 1 country452 target enrollmentSeptember 3, 2019
ConditionsAcute Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Pain
Sponsor
University of Pennsylvania
Enrollment
452
Locations
1
Primary Endpoint
Change in the mean number of pills per opioid prescription
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

In this study, the investigators will evaluate the effect of a health system initiative aiming to change clinician opioid prescribing behaviors using two behavioral economic interventions - individual audit feedback and peer comparison feedback of clinicians.

Detailed Description

Opioid-related abuse and overdose represent a growing national epidemic in the United States. Clinician practice patterns play an important role: opioid prescriptions impact the likelihood that patients will misuse or become dependent on these medications, with longer prescriptions leading to greater sustained use. In this study, we will evaluate a Sutter Health System quality improvement initiative using monthly individual audit feedback and/or monthly peer comparison feedback to clinicians to change opioid prescribing patterns. In partnership with Sutter Health System, this will be conducted using randomization to evaluate its effect. We will also conduct a process evaluation to understand factors associated with better or worse performance at the clinician level.

Registry
clinicaltrials.gov
Start Date
September 3, 2019
End Date
March 2, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Clinicians
  • Practiced primarily at participating emergency department or urgent care center
  • Presented to a participating emergency department or urgent care center during the study period
  • Discharged to home from the visit

Exclusion Criteria

  • Clinicians
  • Saw less than 100 patients in the prior year
  • Practiced primarily at another site that is not in the main trial
  • Did not practice at Sutter Health in the prior 90 days
  • Currently pregnant

Outcomes

Primary Outcomes

Change in the mean number of pills per opioid prescription

Time Frame: Six months

The primary outcome is the change in the mean number of pills prescribed per opioid prescription from baseline to the intervention period.

Secondary Outcomes

  • Change in proportion of patient visits with an opioid prescription(Six months)

Study Sites (1)

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