Online Survey of Clinicians to Learn About Their Interpretation of Capnography Waveforms

This online survey presents capnography waveforms and asks the survey participants to give feedback about their interpretation of the patient status, both in the form of a score and a set of text to describe their interpretation.

Study Overview

• Status: Completed
• Conditions: Clinical Interpretation of Capnography Waveforms
• Intervention / Treatment: Other: Online Survey

Detailed Description

The capnography waveforms presented were originally collected from patients in various clinical settings, with patients both intubated and non-intubated. The de-identified waveforms are presented along with a statement about whether the patients were intubated or not, the amount of supplemental oxygen provided, and in some cases, the oxygen saturation of hemoglobin in the blood (SpO2). The participants are asked to provide a score between 1 and 10 to indicate their interpretation of the wellbeing of the patient. The participants are also asked to provide up to two sentences of text to describe their interpretation of the patient condition based on the information provided.

• Study Type: Observational
• Enrollment (Actual): 75

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

• Sampling Method: Non-Probability Sample

Study Population

Clinicians who have at least two years of experience in interpreting capnography waveforms in their clinical practice

Description

Inclusion Criteria:

• Clinicians who have at least two years of experience in interpreting capnography waveforms in their clinical practice

Exclusion Criteria:

-

Study Plan

How is the study designed?

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Wellbeing score		1 day (survey completion)
Text messages selected by survey participant	Up to two statements describing the interpretation of the condition. For all survey participants, the most commonly preferred text messages will be identified	1 day (survey completion)

Collaborators and Investigators

• Sponsor: University of Utah

Study record dates

Study Major Dates

• Study Start: August 1, 2013
• Primary Completion (Actual): July 1, 2016
• Study Completion (Actual): July 1, 2016

Study Registration Dates

• First Submitted: June 25, 2016
• First Submitted That Met QC Criteria: July 1, 2016
• First Posted (Estimate): July 4, 2016

Study Record Updates

• Last Update Posted (Estimate): July 15, 2016
• Last Update Submitted That Met QC Criteria: July 13, 2016
• Last Verified: July 1, 2016

More Information

Terms related to this study

• Other Study ID Numbers: IRB_00066043

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO