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Clinical Trials/NCT04283214
NCT04283214CompletedNot Applicable

A Comparison of Cardiopulmonary Resuscitation Outcomes Between Traditional and Endomorphic Manikins

North Dakota State University1 site in 1 country50 target enrollmentStarted: February 1, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
50
Locations
1
Primary Endpoint
Compression rate

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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

Arms & Interventions

Traditional manikin

Active Comparator

CPR performed on a traditional manikin

Intervention: Cardiopulmonary Resuscitation (Other)

Traditional manikin with athletic equipment

Experimental

CPR performed on a traditional manikin wearing athletic equipment

Intervention: Cardiopulmonary Resuscitation (Other)

Bariatric manikin

Experimental

CPR performed on a bariatric manikin

Intervention: Cardiopulmonary Resuscitation (Other)

Bariatric manikin with athletic equipment

Experimental

CPR performed on a bariatric manikin wearing athletic equipment

Intervention: Cardiopulmonary Resuscitation (Other)

Outcomes

Primary Outcomes

Compression rate

Time Frame: 2 minutes

number of compressions per minute

Compression rate %

Time Frame: 2 minutes

percent of time compressions are performed at an adequate rate

Compression depth %

Time Frame: 2 minutes

percent of time chest is compressed to adequate depth

Chest recoil

Time Frame: 2 minutes

percent of time chest fully recoils

Compression depth

Time Frame: 2 minutes

average depth of compressions

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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