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

• Sponsor: Hospital Universitario Virgen de la Arrixaca (Other)
• Overall Status: Completed
• CT.gov ID: NCT04357548
• Collaborator: Zoll Medical Corporation (Industry)
• Enrollment: 74
• Location: 1
• Actual Duration (Months): 9.5
• Patients Per Site Per Month: 7.8

Study Details

Study Description

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.

Condition or Disease	Intervention/Treatment	Phase
Cardiopulmonary Resuscitation	Device: FEEDBACK

Study Design

• Study Type: Observational
• Actual Enrollment: 74 participants
• Observational Model: Cohort
• Time Perspective: Prospective
• Official Title: Optimization of Quality in Cardiopulmonary Resuscitation Through Monitor-defibrillator With Feedback System
• Actual Study Start Date: Jan 1, 2019
• Actual Primary Completion Date: Jan 1, 2019
• Actual Study Completion Date: Oct 17, 2019

Arms and Interventions

Arm	Intervention/Treatment
Feedback system 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.	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.

Outcome Measures

Primary Outcome Measures

1. Depth compression [2 minutes]

   Depth of chest compressions performed by the subject

2. Rate compression [2 minutes]

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

3. Quality CPR [2 minutes]

   Total quality of the cardiopulmonary resuscitation performed by the subject

Eligibility Criteria

Criteria

• Ages Eligible for Study: N/A and Older
• Sexes Eligible for Study: 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.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	José Antonio Jiménez Hernández	Murcia		Spain	30120

Sponsors and Collaborators

• Hospital Universitario Virgen de la Arrixaca
• Zoll Medical Corporation

Investigators

• Principal Investigator: Jose Antonio Jimenez Hernandez, Doctor, Hospital Clínico Universitario Virgen de la Arrixaca

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: JOSE ANTONIO JIMENEZ HERNANDEZ, Principal investigator, Hospital Universitario Virgen de la Arrixaca
• ClinicalTrials.gov Identifier: NCT04357548
• Other Study ID Numbers: OPTIMUMCPR
• First Posted: Apr 22, 2020
• Last Update Posted: Apr 22, 2020
• Last Verified: Apr 1, 2020

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by JOSE ANTONIO JIMENEZ HERNANDEZ, Principal investigator, Hospital Universitario Virgen de la Arrixaca: Cardiopulmonary Resuscitation; Feedback; Quality Control

Study Results

No Results Posted as of Apr 22, 2020