Skip to main content
Clinical Trials/NCT03825549
NCT03825549CompletedNot Applicable

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

University of Pennsylvania1 site in 1 country452 target enrollmentStarted: September 3, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
452
Locations
1
Primary Endpoint
Change in the mean number of pills per opioid prescription

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial
Primary Purpose
Health Services Research
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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

Arms & Interventions

Control

No Intervention

No intervention

Individual Audit

Experimental

Clinicians will receive individual audit feedback informing them of their performance.

Intervention: Individual audit feedback (Behavioral)

Peer Comparison

Experimental

Clinicians will receive peer comparison feedback informing them of how their performance compares to their peers.

Intervention: Peer comparison feedback (Behavioral)

Individual Audit and Peer Comparison

Experimental

Clinicians will receive individual audit feedback informing them of their performance and peer comparison feedback informing them of how their performance compares to their peers.

Intervention: Individual audit feedback (Behavioral)

Individual Audit and Peer Comparison

Experimental

Clinicians will receive individual audit feedback informing them of their performance and peer comparison feedback informing them of how their performance compares to their peers.

Intervention: Peer comparison feedback (Behavioral)

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)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials