Skip to main content
Clinical Trials/ISRCTN43049287
ISRCTN43049287
Completed
Not Applicable

A comparison of training packages for deployment of mechanical chest compression devices in clinical practice: a randomised controlled manikin trial (COMPRESS-SIM)

niversity of Warwick0 sites60 target enrollmentJune 30, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
niversity of Warwick
Enrollment
60
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Registry
who.int
Start Date
June 30, 2016
End Date
December 31, 2016
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of Warwick

Eligibility Criteria

Inclusion Criteria

  • 1\. NHS clinical staff (e.g. doctors, nurses, paramedics) that have current registration with a professional body (General Medical Council; Nursing and Midwifery Council; Health and Care Professions Council
  • 2\. Hold a current Resuscitation Council (UK) Immediate Life Support or Advanced Life Support qualification, or other equivalent resuscitation qualification
  • 3\. Provide written informed consent for participation
  • 4\. Prior to randomisation, participants must also have completed the manufacturer on\-line training package on use of the device

Exclusion Criteria

  • 1\. Staff that have an injury or disability that prevents the use or handling of the mechanical chest compression device
  • 2\. Receipt of formal training in use of the LUCAS\-2 mechanical chest compression device in the last six months

Outcomes

Primary Outcomes

Not specified

Similar Trials