Registry of Laypeople's CPR Performance

March 2, 2020 updated by: Enrico Baldi, Pavia nel Cuore

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

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

Study Overview

Status

Unknown

Conditions

Detailed 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.

Study Type

Observational

Enrollment (Anticipated)

10000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 90 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

All the layperson between 18 and 90 years who participate to a BLS/AED course carried out with the use of feedback devices for at least one minute in one of the centers which joined the registry

Description

Inclusion Criteria:

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

Exclusion Criteria:

  • Healthcare personnel

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Percentage of adequate depth compression
Time Frame: 1 minute
Percentage of compression performed between 50 and 60 mm for each participant
1 minute

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mean compression depth
Time Frame: 1 minute
Mean compression depth for each participant
1 minute
Percentage of adequate rate compression
Time Frame: 1 minute
Percentage of compression performed between 100 and 120 per minute for each participant
1 minute
Compression per minute
Time Frame: 1 minute
Number of compressions per minute
1 minute
Percentage of correctly released compression
Time Frame: 1 minute
Percentage of compressions performed with complete chest recoil
1 minute
Percentage of correct hand position
Time Frame: 1 minute
Percentage of compressions performed with hands in the correct position
1 minute

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Pavia nel Cuore

Collaborators

Robbio nel Cuore

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2016

Primary Completion (Anticipated)

December 31, 2020

Study Completion (Anticipated)

December 31, 2020

Study Registration Dates

First Submitted

June 9, 2017

First Submitted That Met QC Criteria

June 9, 2017

First Posted (Actual)

June 14, 2017

Study Record Updates

Last Update Posted (Actual)

March 4, 2020

Last Update Submitted That Met QC Criteria

March 2, 2020

Last Verified

March 1, 2020

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • FeedbackRegistry

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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