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Capnography At the Bedside: Leading Educational Efforts

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02901197
Acronym
CapABLE
Enrollment
902
Registered
2016-09-15
Start date
2016-09-15
Completion date
2017-10-17
Last updated
2018-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emergency

Keywords

capnography

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: 1. the effect of a comprehensive theory-based educational intervention on staff knowledge and skills related to capnography (outcome measure). 2. 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). 3. 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.

Interventions

BEHAVIORALEducation and Reminder Posters

See arm description

See arm description

Sponsors

Medtronic - MITG
CollaboratorINDUSTRY
Yale University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Average Monitoring FrequencyPre intervention 3 months and Post intervention about 6 monthsThis outcome will reflect the number of patients the staff applied the monitoring to pre and post intervention.

Secondary

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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026