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Clinical Practice Guidelines and Impact of Audit and Feedback in the Emergency Department

Primary Purpose

Shock, Septic, Community Acquired Pneumonia

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Feedback with Peer Comparison
Sponsored by
Denver Health and Hospital Authority
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Shock, Septic focused on measuring Clinical Practice Guidelines

Eligibility Criteria

30 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Attending emergency medicine physicians working clinically in the Adult Emergency Department at Denver Health Medical Center at the start of the study.

Exclusion Criteria:

  • None. All eligible physicians will be included.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    No Intervention

    Experimental

    Arm Label

    Pre-Intervention

    Feedback with Peer Comparison

    Arm Description

    Delayed feedback and peer comparison

    Individualized adherence feedback with peer comparison

    Outcomes

    Primary Outcome Measures

    Change in Adherence to Community-Acquired Pneumonia and Severe Sepsis Clinical Practice Guidelines
    Adherence will be determined via chart review of patients and will be measured by concordance with published clinical practice guidelines

    Secondary Outcome Measures

    Full Information

    First Posted
    April 15, 2015
    Last Updated
    February 1, 2017
    Sponsor
    Denver Health and Hospital Authority
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02427048
    Brief Title
    Clinical Practice Guidelines and Impact of Audit and Feedback in the Emergency Department
    Official Title
    Adherence to Clinical Practice Guidelines and the Impact of Audit and Feedback in the Emergency Department
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2017
    Overall Recruitment Status
    Completed
    Study Start Date
    July 2015 (undefined)
    Primary Completion Date
    April 2016 (Actual)
    Study Completion Date
    December 2016 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Denver Health and Hospital Authority

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This study will develop and test an intervention given to emergency medicine providers to improve adherence to clinical practice guidelines (CPGs) for pneumonia and sepsis.
    Detailed Description
    This study will be performed at Denver Health Medical Center, a 477-bed urban, safety-net, acute-care hospital located in Denver, Colorado. The adult ED is staffed by board-certified emergency physicians at all times. These physicians supervise the care of all patients being managed by resident physicians, nurse practitioners, physician assistants, and medical students. Approximately 430 patients are admitted to the hospital from the ED each year with community-acquired pneumonia (CAP) and severe sepsis (SS). Adherence to CPGs will be measured at the level of the attending emergency physician. All employed, attending emergency physicians working clinically in the adult ED at Denver Health Medical Center at the start of the study will be included. The investigators will use a step-wedge design to randomize physicians into clusters. Randomization of physicians into clusters and randomization of clusters to intervention timing will occur one week prior to delivery of the intervention to cluster one. he intervention will consist of monthly audit and feedback on adherence to CPGs for CAP and SS. Once a cluster enters its first intervention month, all physicians in that cluster will receive an email detailing their adherence to both CAP and SS CPG for every month since the start of the study. Adherence to the entire CPG as well as each component of the CPG will be provided. In addition, physicians will be shown the median prevalence of adherence for all physicians as well as where their adherence ranks among their physician group. Lastly, in a separate secure email, physicians will be given patient identifiers (i.e., name, MRN, date of visit) for each patient that received non-adherent care and will be told which component of care was not adherent to the respective CPG so that they can review the case themselves, if desired.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Shock, Septic, Community Acquired Pneumonia
    Keywords
    Clinical Practice Guidelines

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    Investigator
    Allocation
    Randomized
    Enrollment
    24 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Pre-Intervention
    Arm Type
    No Intervention
    Arm Description
    Delayed feedback and peer comparison
    Arm Title
    Feedback with Peer Comparison
    Arm Type
    Experimental
    Arm Description
    Individualized adherence feedback with peer comparison
    Intervention Type
    Behavioral
    Intervention Name(s)
    Feedback with Peer Comparison
    Intervention Description
    Email detailing adherence to CAP and SS CPG for every month since start of study. Physicians will be provided individualized feedback and given patient identifiers for each patient that received non-adherent care.
    Primary Outcome Measure Information:
    Title
    Change in Adherence to Community-Acquired Pneumonia and Severe Sepsis Clinical Practice Guidelines
    Description
    Adherence will be determined via chart review of patients and will be measured by concordance with published clinical practice guidelines
    Time Frame
    30 days post-intervention and 60 days post-intervention

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    30 Years
    Maximum Age & Unit of Time
    70 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Attending emergency medicine physicians working clinically in the Adult Emergency Department at Denver Health Medical Center at the start of the study. Exclusion Criteria: None. All eligible physicians will be included.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Stacy Trent, MD
    Organizational Affiliation
    Denver Health and Hospital Authority
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Clinical Practice Guidelines and Impact of Audit and Feedback in the Emergency Department

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