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A Comparison of CPR Outcomes Between Traditional and Endomorphic Manikins With and Without Equipment

Not Applicable
Completed
Conditions
Cardiac Arrest
Interventions
Other: Cardiopulmonary Resuscitation
Registration Number
NCT04283214
Lead Sponsor
North Dakota State University
Brief Summary

The study's research design is a randomized experiment. 50 emergency responders (emergency medical responders, emergency medical technicians, advanced emergency medical technicians, and paramedics) will be recruited for this research. All data collection will take place in Lab 14 of the Benson Bunker Fieldhouse or a professional, confidential location of the participant's choosing.

Prior to CPR performance, participants will be given an informed consent form to sign. The form will be explained in detail by the researcher collecting data. After obtaining informed consent, participants will be asked to fill out a demographic questionnaire to collect information such as age, gender, years of emergency responder experience/employment, and years of CPR certification. Demographic information provided by participants will be utilized in data analysis. The demographics form should take approximately five minutes to complete. Participants will be randomly assigned to the four trials they will partake in and instructed via oral script (one for over and one for under football shoulder pads) to perform four-trials total of three-minute single-rescuer CPR on both a traditional CPR manikin and "Fat Old Fred" (bariatric) CPR manikin. CPR must be performed in accordance with the American Heart Association's 2015 CPR Guidelines and participants will use a CPRmeter 2 device to collect data to determine the quality of CPR components (chest compression depth/recoil, compression rate, CPR compression duration, mean depth, mean rate, and total number of compressions). The entire study session should take 25 to 30 minutes to complete.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
Inclusion Criteria
  • Emergency responders employed through the ambulance stations located in North Dakota and Minnesota
  • Current CPR/first-aid certification
  • Active clinician, educator, or administrator.
Exclusion Criteria
  • Cardiovascular conditions inhibiting CPR performance
  • Respiratory conditions inhibiting CPR performance
  • Musculoskeletal conditions inhibiting CPR performance

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
Bariatric manikinCardiopulmonary ResuscitationCPR performed on a bariatric manikin
Traditional manikinCardiopulmonary ResuscitationCPR performed on a traditional manikin
Bariatric manikin with athletic equipmentCardiopulmonary ResuscitationCPR performed on a bariatric manikin wearing athletic equipment
Traditional manikin with athletic equipmentCardiopulmonary ResuscitationCPR performed on a traditional manikin wearing athletic equipment
Primary Outcome Measures
NameTimeMethod
Compression rate2 minutes

number of compressions per minute

Compression rate %2 minutes

percent of time compressions are performed at an adequate rate

Compression depth %2 minutes

percent of time chest is compressed to adequate depth

Chest recoil2 minutes

percent of time chest fully recoils

Compression depth2 minutes

average depth of compressions

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

North Dakota State University

🇺🇸

Fargo, North Dakota, United States

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