Registry of Laypeople's CPR Performance

Quality of Cardio-pulmonary Resuscitation Clinical Trial

Official title:

International Registry of Laypeople's CPR Performance After Training With Feedback Devices

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03185260
• Other study ID #: FeedbackRegistry
• Status: Recruiting
• Start date: May 1, 2016
• Est. completion date: December 31, 2020

Study information

• Verified date: March 2020
• Source: Pavia nel Cuore
• Contact: Enrico Baldi, MD
• Email: enrico.baldi[@]pavianelcuore.it
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

The aim of the registry is to collect laypeople's performance after a BLS/AED course carried out with the use of feedback devices.

Description:

The registry collect all the laypeople's performance of 1-minute of chest-compression only CPR registered at the end of a CPR/AED course in which feedback devices were used for at least 1 minute.

All centers which carry out BLS/AED course for laypeople using CPR feedback devices can join to the registry.

All the centers have to declare the duration of the course, the guidelines followed, the participants' anthropometric variables and the feedback device they used for the course and for the test.

The centers must send the performances of all the participants of a course.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 10000
• Est. completion date: December 31, 2020
• Est. primary completion date: December 31, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

• Layperson

• Participating in a BLS/AED course carried out with feedback devices

Exclusion Criteria:

• Healthcare personnel

Related Conditions & MeSH terms

• Quality of Cardio-pulmonary Resuscitation

Locations

Country	Name	City	State
Italy	Policlinico P. Giaccone	Palermo
Italy	Pavia nel Cuore	Pavia
Italy	Robbio nel Cuore	Robbio	Pavia
Switzerland	FormaMed	Cortaillod
Switzerland	ES ASUR	Le Mont-sur-Lausanne

Sponsors (2)

Lead Sponsor	Collaborator
Pavia nel Cuore	Robbio nel Cuore

Countries where clinical trial is conducted

Italy,  Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage of adequate depth compression	Percentage of compression performed between 50 and 60 mm for each participant	1 minute
Secondary	Mean compression depth	Mean compression depth for each participant	1 minute
Secondary	Percentage of adequate rate compression	Percentage of compression performed between 100 and 120 per minute for each participant	1 minute
Secondary	Compression per minute	Number of compressions per minute	1 minute
Secondary	Percentage of correctly released compression	Percentage of compressions performed with complete chest recoil	1 minute
Secondary	Percentage of correct hand position	Percentage of compressions performed with hands in the correct position	1 minute