COMPRESS-SIM study

  • Research type

    Research Study

  • Full title

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

  • IRAS ID

    199172

  • Contact name

    Keith Couper

  • Contact email

    k.couper@warwick.ac.uk

  • Sponsor organisation

    University of Warwick

  • Duration of Study in the UK

    0 years, 6 months, 17 days

  • Research summary

    Patients that have a cardiac arrest require immediate treatment with chest compressions. To deliver chest compressions, the rescuer must press forcefully on the breastbone approximately 100 times per minute. This can quickly become exhausting for the rescuer.

    Machines that can deliver chest compressions have been developed. These machines can consistently deliver high quality chest compressions and, unlike humans, do not get tired. However, fitting these machines on the patient can be difficult. It is important that doctors and nurses are trained as well as possible to help them use these devices effectively. Some studies suggest that training based on the formula one motor racing pit-crew may be better than standard training approaches on how to use these devices.

    We plan a study to work out whether this new pit-crew training method is more effective than standard training. Standard training consists of an overview of the device, as well as the chance to practice using it. In pit-crew training, teams will also get a formal protocol to use to help them use the device. We will recruit 20 teams of three doctors/ nurses (total 60 doctors/ nurses). Each team will be allocated by chance to receive either standard training or the pit-crew training. Following the training, the teams will then complete a test in which they treat a manikin. The results of this test will help us work out which training method is more effective.

    The results of this study will help us work out the best way to train doctors and nurses in how to use these devices in the future.

  • REC name

    N/A

  • REC reference

    N/A