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Capnography At the Bedside: Leading Educational Efforts (CapABLE)

Primary Purpose

Emergency

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Education and Reminder Posters
Policy Change
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Emergency focused on measuring capnography

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Emergency department (ED) staff
  • Staff will include registered nurses, respiratory therapists, technical associates, physicians, physician's assistants and advanced practice nurse practitioners who fulfill the majority of their clinical duties in the ED.

Exclusion Criteria:

  • Staff who are assigned to work on other units, but who work in the ED on a casual or per diem status will be excluded.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    Education and Reminder

    Policy Change

    Arm Description

    This arm will consist of participants in a location that receive with web based training and exposure to reminder posters in the workplace.

    This arm's participants will not receive an active intervention (education and reminders), however, policy change will take place in this location.

    Outcomes

    Primary Outcome Measures

    Average Monitoring Frequency
    This outcome will reflect the number of patients the staff applied the monitoring to pre and post intervention.

    Secondary Outcome Measures

    Knowledge
    A tool will be developed as part of the study to assess knowledge and how that might change over time (from pre to post)
    Knowledge
    A tool will be developed as part of the study to assess knowledge and how that might change over time (from pre to post)

    Full Information

    First Posted
    September 9, 2016
    Last Updated
    August 20, 2018
    Sponsor
    Yale University
    Collaborators
    Medtronic - MITG
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02901197
    Brief Title
    Capnography At the Bedside: Leading Educational Efforts
    Acronym
    CapABLE
    Official Title
    Capnography At the Bedside: Leading Educational Efforts (CapABLE Trial)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    September 15, 2016 (Actual)
    Primary Completion Date
    September 15, 2017 (Actual)
    Study Completion Date
    October 17, 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Yale University
    Collaborators
    Medtronic - MITG

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The purpose of this dual-site quasi-experimental pilot study is to evaluate if the implementation of an educational intervention paired with an environmental assessment to address accessibility barriers is associated with improvement in staff knowledge and skills, and adherence to national guidelines for use (evaluation in the knowledge transfer framework) in an emergency department (ED) setting.
    Detailed Description
    The objective of this study is to develop a multi-faceted implementation program (referred to as the Capnography At the Bedside: Leading Emergency Education (CapABLE Trial)) to increase the use of capnography during two critical events in the emergency department, intubation and CPR, for better detection of endotracheal intubation, endotracheal tube dislodgement, and quality CPR. The specific aims of the proposed study are to examine: the effect of a comprehensive theory-based educational intervention on staff knowledge and skills related to capnography (outcome measure). the effect of a multi-faceted implementation program on the adherence to national guidelines regarding the use of capnography during critical events in the emergency department (process measure). the sustainability of effects of the implementation program on adherence, knowledge and skills (outcome and process measure). The design and methods of this study are based on the knowledge transfer framework, which dictates identification of the message, target audience, messenger, process and communication, and evaluation.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Emergency
    Keywords
    capnography

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    Education and Reminder
    Arm Type
    Active Comparator
    Arm Description
    This arm will consist of participants in a location that receive with web based training and exposure to reminder posters in the workplace.
    Arm Title
    Policy Change
    Arm Type
    Active Comparator
    Arm Description
    This arm's participants will not receive an active intervention (education and reminders), however, policy change will take place in this location.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Education and Reminder Posters
    Intervention Description
    See arm description
    Intervention Type
    Other
    Intervention Name(s)
    Policy Change
    Intervention Description
    See arm description
    Primary Outcome Measure Information:
    Title
    Average Monitoring Frequency
    Description
    This outcome will reflect the number of patients the staff applied the monitoring to pre and post intervention.
    Time Frame
    Pre intervention 3 months and Post intervention about 6 months
    Secondary Outcome Measure Information:
    Title
    Knowledge
    Description
    A tool will be developed as part of the study to assess knowledge and how that might change over time (from pre to post)
    Time Frame
    Pre intervention
    Title
    Knowledge
    Description
    A tool will be developed as part of the study to assess knowledge and how that might change over time (from pre to post)
    Time Frame
    Post intervention (within 1 month of intervention)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Emergency department (ED) staff Staff will include registered nurses, respiratory therapists, technical associates, physicians, physician's assistants and advanced practice nurse practitioners who fulfill the majority of their clinical duties in the ED. Exclusion Criteria: Staff who are assigned to work on other units, but who work in the ED on a casual or per diem status will be excluded.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Melissa Langhan, MD
    Organizational Affiliation
    Yale University Dept of Pediatrics, Section of Emergency Medicine
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided
    Citations:
    PubMed Identifier
    32175968
    Citation
    Shah R, Streat DA, Auerbach M, Shabanova V, Langhan ML. Improving Capnography Use for Critically Ill Emergency Patients: An Implementation Study. J Patient Saf. 2022 Jan 1;18(1):e26-e32. doi: 10.1097/PTS.0000000000000683.
    Results Reference
    derived

    Learn more about this trial

    Capnography At the Bedside: Leading Educational Efforts

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