Incentivizing Buprenorphine-Naloxone Initiation in Emergency Departments
Opioid Use

About this trial
This is an interventional health services research trial for Opioid Use
Eligibility Criteria
Inclusion Criteria:
- Residents and Advanced Practice Providers and attending clinicians working in emergency departments in Pennsylvania.
Exclusion Criteria:
-
Sites / Locations
- University of Pennsylvania Health System
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Standard training arm
Behavioral economic enhanced arm
The standard training arm will consist of (1) in-person training with pre- and post-session knowledge and attitude assessment, (2) three month post-session knowledge and attitude assessment and (3) self-report of first-time buprenorphine-naloxone Emergency Department administration within 3 month study period.
The behavioral economic enhanced training arm will consist of (1) in-person training with pre- and post-session knowledge and attitude assessment, (2) three month post-session knowledge and attitude assessment and (3) self-report of first-time buprenorphine-naloxone Emergency Department administration within 3 month study period in addition to an opt-out invitation, loss-framed incentivization, and weekly tailored text message-based reminders