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OpenTrials
Completed

NCT Number: NCT02901197

Capnography At the Bedside: Leading Educational Efforts

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

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

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.

Treatment and study plan

Education and Reminder Posters

Behavioral

See arm description

Policy Change

Other

See arm description

Primary outcomes

  1. Average Monitoring Frequency

    Time frame: Pre intervention 3 months and Post intervention about 6 months

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

Secondary outcomes

  1. Knowledge

    Time frame: Pre intervention

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

  2. Knowledge

    Time frame: Post intervention (within 1 month of intervention)

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

Sponsors and collaborators

Lead sponsor

Yale University

Other

Collaborators

  • Medtronic - MITG

Registry information

Official study title

Capnography At the Bedside: Leading Educational Efforts (CapABLE Trial)

Acronym: CapABLE

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Sep 15, 2016
Registry last updated
Aug 22, 2018

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.

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