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PRescribing INterventions for Chronic Pain Via the Electronic Health Record Study - Opioid-Naive Population (PRINCE)

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Completed

Conditions

Opioid-use Disorder
Opioid Abuse
Opioid Use

Treatments

Behavioral: Choice Architecture Nudge
Behavioral: PMP Integration & Nudge

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04601493
STUDY00006522-2
R33DA046084 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The objective of this research is to assess the effects of electronic health record (EHR)-based decision support tools on primary care provider (PCP) decision-making around pain treatment and opioid prescribing. The decision support tools are informed by principles of "behavioral economics," whereby clinicians are "nudged," though never forced, towards guideline-concordant care.

Full description

To test the effects of these decision support tools for improving the quality of care for pain treatment, the investigators will implement a pragmatic clinic-randomized trial across the primary care clinics of Fairview Medical Group and University of Minnesota Physicians.

The study has two parallel components. The decision support tools to be tested will differ somewhat depending on whether a given patient is opioid-naïve, or whether a given patient is a current opioid-user. Four sets of analyses will be conducted separately: one for the opioid-naïve group using EHR data, one for the current opioid-user group using EHR data, one at the PCP-level using web survey data, and one at the PCP-level using MN Prescription Drug Monitoring Program (PDMP) data.

Enrollment

631 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All primary care providers from all of the Fairview and University of Minnesota Physicians study clinics

Exclusion criteria

  • Primary care providers who work less than 20% full time equivalent (FTE)

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

631 participants in 4 patient groups

Care as Usual
No Intervention group
Description:
Clinics assigned to this arm will continue to care for the patients as usual in regards to opioid prescribing.
Choice Architecture Nudge
Experimental group
Description:
Clinics in this arm will receive the choice architecture nudge intervention.
Treatment:
Behavioral: Choice Architecture Nudge
PMP Integration & Nudge
Experimental group
Description:
Clinics in this arm will receive the Prescription Drug Monitoring (PMP) Integration \& Nudge intervention.
Treatment:
Behavioral: PMP Integration & Nudge
Choice Architecture Nudge + PMP Integration & Nudge
Experimental group
Description:
Clinics in this arm will receive both the choice architecture nudge and prescription drug monitoring (PMP) integration \& nudge interventions.
Treatment:
Behavioral: PMP Integration & Nudge
Behavioral: Choice Architecture Nudge

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Ezra Golberstein, PhD

Data sourced from clinicaltrials.gov

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