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

NCT04357548 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 74

Last updated 2020-04-22

No results posted yet for this study

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.

Conditions

  • Cardiopulmonary Resuscitation

Interventions

DEVICE

FEEDBACK

Once the sample was selected, a test was performed in which the professionals performed 2 minutes of CPR on the dummy without any feedback system, after 5 minutes they performed 2 minutes of CPR with feedback system through the Zoll® monitor with CPR patch -D padz training, to later compare the pretest-posttest results.

Sponsors & Collaborators

  • Zoll Medical Corporation

    collaborator INDUSTRY

  • Hospital Universitario Virgen de la Arrixaca

    lead OTHER

Principal Investigators

  • Jose Antonio Jimenez Hernandez, Doctor · Hospital Universitario Virgen de la Arrixaca

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-01-01
Primary Completion
2019-01-01
Completion
2019-10-17

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04357548 on ClinicalTrials.gov