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Clinical Trials/NCT04357548
NCT04357548CompletedNot Applicable

Optimization of Quality in Cardiopulmonary Resuscitation Through Monitor-defibrillator With Feedback System

Hospital Universitario Virgen de la Arrixaca1 site in 1 country74 target enrollmentStarted: January 1, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
74
Locations
1
Primary Endpoint
Rate compression

Study Overview

Brief Summary

AIM: To verify the effect of a feedback system on optimizing quality during CPR on mannequins.

Hypothesis: The quality of CPR performed by healthcare professionals through a defibrillator monitor with a feedback system is higher than those that do not use a feedback system on a manikin.

METHOD Type of study: Pre-experimental with pretest-postest design. Sample: Health professionals of the General Emergency Service of the Virgen de la Arrixaca University Hospital (HCUVA).

Sampling type: Non-probabilistic for convenience. Variables: sex, age, profession, years of experience, last CPR training received, last time performing CPR, depth, frequency, quality CPR, perception of the quality of CPR.

Statistical analysis: Student's t for related samples and McNemar.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Health professionals working in the General Emergency Service of the Virgen de la Arrixaca University Clinical Hospital during the study period. They include doctors, resident doctors, and nurses.
  • Health professionals from the General Emergency Service of the Virgen de la Arrixaca University Hospital who receive the training session on CPR quality and use of the defibrillator monitor with feedback system.

Exclusion Criteria

  • Health professionals who do not work in the General Emergency Service of the Virgen de la Arrixaca University Clinical Hospital during the study period.
  • Health professionals who work in the General Emergency Service of the Virgen de la Arrixaca University Hospital and refuse to carry out the training and demonstration session.

Outcomes

Primary Outcomes

Rate compression

Time Frame: 2 minutes

Frequency of the number of chest compressions per minute performed by the subject

Quality CPR

Time Frame: 2 minutes

Total quality of the cardiopulmonary resuscitation performed by the subject

Depth compression

Time Frame: 2 minutes

Depth of chest compressions performed by the subject

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Hospital Universitario Virgen de la Arrixaca
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

JOSE ANTONIO JIMENEZ HERNANDEZ

Principal investigator

Hospital Universitario Virgen de la Arrixaca

Study Sites (1)

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