NCT04357548

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
74

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2019

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2019

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2019

Completed
10 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 17, 2019

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

April 17, 2020

Completed
5 days until next milestone

First Posted

Study publicly available on registry

April 22, 2020

Completed
Last Updated

April 22, 2020

Status Verified

April 1, 2020

Enrollment Period

Same day

First QC Date

April 17, 2020

Last Update Submit

April 21, 2020

Conditions

Keywords

Cardiopulmonary ResuscitationFeedbackQuality Control

Outcome Measures

Primary Outcomes (3)

  • Depth compression

    Depth of chest compressions performed by the subject

    2 minutes

  • Rate compression

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

    2 minutes

  • Quality CPR

    Total quality of the cardiopulmonary resuscitation performed by the subject

    2 minutes

Study Arms (1)

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

Interventions

FEEDBACKDEVICE

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.

Feedback system

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Subjects belonging to the General Emergency Department of the Hospital Clinico Universitario Virgen de la Arrixaca corresponding with doctors, resident doctors and nurses who are working in the service during the study period and receive the training session on CPR quality and the use of the defibrillator monitor with feedback system

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

José Antonio Jiménez Hernández

Murcia, 30120, Spain

Location

Study Officials

  • Jose Antonio Jimenez Hernandez, Doctor

    Hospital Universitario Virgen de la Arrixaca

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

April 17, 2020

First Posted

April 22, 2020

Study Start

January 1, 2019

Primary Completion

January 1, 2019

Study Completion

October 17, 2019

Last Updated

April 22, 2020

Record last verified: 2020-04

Data Sharing

IPD Sharing
Will not share

Locations