Skip to main content
OpenTrials
Completed

NCT Number: NCT02665429

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UMass Clinton Hospital, Clinton, Massachusetts, United States

Loading trial locations.

About this study

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).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Individual prescribing data profile and self-assessment

Behavioral

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 outcomes

  1. 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 outcomes

  1. 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

  2. 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

  3. 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 outcomes

  1. Self-assessment of decile for number of opioid prescriptions per hundred patients seen

    Time frame: Once, at time of enrollment

    The provider's self-assessment of their decile of number of opioid prescriptions per hundred patients seen, compared to their peers

  2. Self-assessment of decile for percentage of total prescriptions written that are opioids

    Time frame: Once, at time of enrollment

    The provider's self-assessment of their decile of their percentage of total prescriptions written that are opioids, compared to their peers

  3. Self-assessment of decile for median quantity of pills dispensed per opioid prescription

    Time frame: Once, at time of enrollment

    The provider's self-assessment of their decile of their median quantity of pills dispensed per opioid prescription, compared to their peers

  4. Self-assessment of decile for number of prescriptions for long-acting opioid formulations

    Time frame: Once, at time of enrollment

    The provider's self-assessment of their decile of their number of prescriptions for long-acting opioid formulations, compared to their peers

Sponsors and collaborators

Lead sponsor

University of Massachusetts, Worcester

Other

Collaborators

  • UMass Memorial Health

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Jan 27, 2016
Registry last updated
Jun 27, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.