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
2018 results in https://www.ncbi.nlm.nih.gov/pubmed/29391379
Investigators
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
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