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

Cardiopulmonary Resuscitation Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04357548
• Other study ID #: OPTIMUMCPR
• Status: Completed
• Start date: January 1, 2019
• Est. completion date: October 17, 2019

Study information

• Verified date: April 2020
• Source: Hospital Universitario Virgen de la Arrixaca
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 74
• Est. completion date: October 17, 2019
• Est. primary completion date: January 1, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

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.

Related Conditions & MeSH terms

• Cardiopulmonary Resuscitation

Intervention

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.

Locations

Country	Name	City	State
Spain	José Antonio Jiménez Hernández	Murcia

Sponsors (2)

Lead Sponsor	Collaborator
Hospital Universitario Virgen de la Arrixaca	Zoll Medical Corporation

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Depth compression	Depth of chest compressions performed by the subject	2 minutes
Primary	Rate compression	Frequency of the number of chest compressions per minute performed by the subject	2 minutes
Primary	Quality CPR	Total quality of the cardiopulmonary resuscitation performed by the subject	2 minutes