search
Back to results

A Quality Improvement Project to Investigate Individual Provider Variation in Opioid Prescribing From the Emergency Department

Primary Purpose

Analgesics, Opioid, Delivery of Health Care, Drug Prescribing

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Individual prescribing data profile and self-assessment
Sponsored by
University of Massachusetts, Worcester
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Analgesics, Opioid focused on measuring Emergency Medicine

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Provider who practices Emergency Medicine in one or more of four UMass-affiliated EDs (UMassMemorial Medical Center, Marlborough Hospital, and Clinton Hospital), including attending physicians, resident physicians, and advanced practice providers (PAs and NPs).
  • Have placed at least one electronic prescription for a medication of interest (namely opioids) in the PulseCheck electronic medical record system during the 12 months prior to the implementation of the opioid guidelines
  • Be actively practicing in a UMass-affiliated ED at time of implementation of the guidelines

Exclusion Criteria:

  • None

Sites / Locations

  • UMass Clinton Hospital
  • UMass Memorial Marlborough Hospital
  • UMass Memorial Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control

Intervention

Arm Description

Providers who are subject only to the routine implementation of clinical practice guidelines without additional experimental intervention

Providers who are subject to routine clinical practice guideline implementation AND receive provider's own individual prescribing data profile intervention ("Individual prescribing data profile and self-assessment")

Outcomes

Primary Outcome Measures

Change in number of opioid prescriptions per hundred patients seen

Secondary Outcome Measures

Change in percentage of total prescriptions written that are opioids
Change in median quantity of pills dispensed per opioid prescription
Change in number of prescriptions for long-acting opioid formulations

Full Information

First Posted
January 20, 2016
Last Updated
June 23, 2017
Sponsor
University of Massachusetts, Worcester
Collaborators
UMass Memorial Health Care
search

1. Study Identification

Unique Protocol Identification Number
NCT02665429
Brief Title
A Quality Improvement Project to Investigate Individual Provider Variation in Opioid Prescribing From the Emergency Department
Official Title
A Quality Improvement Project to Investigate Individual Provider Variation in Opioid Prescribing From the Emergency Department
Study Type
Interventional

2. Study Status

Record Verification Date
June 2017
Overall Recruitment Status
Completed
Study Start Date
February 1, 2016 (Actual)
Primary Completion Date
March 1, 2017 (Actual)
Study Completion Date
March 1, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Massachusetts, Worcester
Collaborators
UMass Memorial Health Care

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a study of emergency physicians' prescribing patterns related to opioid (narcotic) medications. We are trying to determine whether giving providers access to their own prescribing data influences their prescribing patterns.
Detailed Description
Opioid misuse is a known public safety threat and public health problem, both nationwide and in the Commonwealth of Massachusetts. As a part of these efforts, Emergency Department (ED) outpatient prescriptions have been identified as a potential area for improvement. The Massachusetts Hospital Association (MHA), in conjunction with other stakeholders, developed a set of recommendations to address opioid management and prescribing within the ED setting. This study is timed to coincide with the rollout by UMassMemorial Health Care of a system-wide opioid prescribing practice guideline/policy which mirrors the Massachusetts Hospital Association's guideline. This rollout provides a unique opportunity for a natural experiment related to provider prescribing practices. This is a quality improvement project with two primary objectives: Improve understanding of physician practice patterns related to emergency department (ED) opioid prescribing Evaluate the effectiveness of providing individual clinician profile data in influencing behavior change among ED providers, as it relates to their opioid prescribing patterns There are two corresponding specific aims: Quantitatively describe the current state of opioid prescribing by ED clinicians at four UMass Memorial EDs (using prescriptions generated within the ED electronic health information system between February 2014 and the study implementation date). Descriptive statistics being considered for feasibility of study include: Number of opioid prescriptions per hundred patients seen Percentage of total prescriptions written that are opioids Mean or median quantity of pills dispensed per opioid prescription Number of prescriptions for long-acting opioid formulations Evaluate the effect on prescribing practices of providing individual clinicians with their profile data to illustrate their personal opioid prescribing patterns, relative to the de-identified distribution for all other clinicians in the ED group This project is timed to coincide with the separately planned implementation of a system-wide opioid prescribing guideline. The guideline implementation is an independent event, but we feel that it presents a unique opportunity for a simultaneous experimental intervention to assess whether providing clinicians with their individual data alters their prescribing practices beyond any effect achieved simply by being subject to the new guideline. Data collected from the electronic medical record and clinician self-reported data about their perceptions of their prescribing practices will be used to evaluate both the effect of the guideline implementation (i.e. comparison of prescribing patterns for all clinicians before and after guideline implementation) and the combined effect of guideline implementation plus individual profile intervention (i.e. comparisons across intervention versus control groups).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Analgesics, Opioid, Delivery of Health Care, Drug Prescribing, Over Prescribing, Prescribing Patterns, Physician, Practice Management, Medical, Practice Guidelines as Topic
Keywords
Emergency Medicine

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
109 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Providers who are subject only to the routine implementation of clinical practice guidelines without additional experimental intervention
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Providers who are subject to routine clinical practice guideline implementation AND receive provider's own individual prescribing data profile intervention ("Individual prescribing data profile and self-assessment")
Intervention Type
Behavioral
Intervention Name(s)
Individual prescribing data profile and self-assessment
Intervention Description
Prior to receiving his or her individual data profile, each provider in the intervention group will be asked to identify his or her self-assessment of his or her own opioid prescribing practices. Immediately after providing self-perception data, providers will be provided with their true profile data with a visual display of where they fall within the distribution of their peers. All peer data are de-identified.
Primary Outcome Measure Information:
Title
Change in number of opioid prescriptions per hundred patients seen
Time Frame
Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention
Secondary Outcome Measure Information:
Title
Change in percentage of total prescriptions written that are opioids
Time Frame
Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention
Title
Change in median quantity of pills dispensed per opioid prescription
Time Frame
Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention
Title
Change in number of prescriptions for long-acting opioid formulations
Time Frame
Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention
Other Pre-specified Outcome Measures:
Title
Self-assessment of decile for number of opioid prescriptions per hundred patients seen
Description
The provider's self-assessment of their decile of number of opioid prescriptions per hundred patients seen, compared to their peers
Time Frame
Once, at time of enrollment
Title
Self-assessment of decile for percentage of total prescriptions written that are opioids
Description
The provider's self-assessment of their decile of their percentage of total prescriptions written that are opioids, compared to their peers
Time Frame
Once, at time of enrollment
Title
Self-assessment of decile for median quantity of pills dispensed per opioid prescription
Description
The provider's self-assessment of their decile of their median quantity of pills dispensed per opioid prescription, compared to their peers
Time Frame
Once, at time of enrollment
Title
Self-assessment of decile for number of prescriptions for long-acting opioid formulations
Description
The provider's self-assessment of their decile of their number of prescriptions for long-acting opioid formulations, compared to their peers
Time Frame
Once, at time of enrollment

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Provider who practices Emergency Medicine in one or more of four UMass-affiliated EDs (UMassMemorial Medical Center, Marlborough Hospital, and Clinton Hospital), including attending physicians, resident physicians, and advanced practice providers (PAs and NPs). Have placed at least one electronic prescription for a medication of interest (namely opioids) in the PulseCheck electronic medical record system during the 12 months prior to the implementation of the opioid guidelines Be actively practicing in a UMass-affiliated ED at time of implementation of the guidelines Exclusion Criteria: None
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sean Michael, MD
Organizational Affiliation
UMass Memorial Health Care
Official's Role
Principal Investigator
Facility Information:
Facility Name
UMass Clinton Hospital
City
Clinton
State/Province
Massachusetts
Country
United States
Facility Name
UMass Memorial Marlborough Hospital
City
Marlborough
State/Province
Massachusetts
Country
United States
Facility Name
UMass Memorial Medical Center
City
Worcester
State/Province
Massachusetts
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

A Quality Improvement Project to Investigate Individual Provider Variation in Opioid Prescribing From the Emergency Department

We'll reach out to this number within 24 hrs