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

About this trial
This is an interventional health services research trial for Emergency focused on measuring capnography
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.
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
NCT ID
NCT02901197
First Posted
September 9, 2016
Last Updated
August 20, 2018
Sponsor
Yale University
Collaborators
Medtronic - MITG
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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