Wearable Aurora watch system for syncope assessment : a pilot study

  • Research type

    Research Study

  • Full title

    Aurora cardiovascular watch system: a pilot study in patients with suspected syncope undergoing formal falls and syncope investigation

  • IRAS ID

    208250

  • Contact name

    John Allen

  • Contact email

    john.allen@nuth.nhs.uk

  • Sponsor organisation

    Joint Research Office

  • Duration of Study in the UK

    0 years, 8 months, 30 days

  • Research summary

    The Aurora watch is a new wearable system with capability for measuring signals that allow the assessment of cardiovascular health. Its main function is to measure, non-invasively, the pressure pulse at the wrist. It can also measure the electrocardiogram (ECG – heart trace) which can make the analysis of the waveforms easier. It is easy to make measurements - with the watchstrap simply attached to the wrist, the measurements stored and then analysed after they have been collected using a dedicated software programme. We are undertaking a pilot study to see if the Aurora cardiovascular information may be of use when investigating patients who experience syncope (fainting) or unexplained falls. The potential for the device to be used outside of the clinic is a key novel aspect. However, we initially aim to undertake a pilot study of the Aurora watch in conjunction with current standard testing for patients referred to the Newcastle upon Tyne Falls and Syncope Service (FASS). This is in order to determine if the watch system can detect the same types of physiological changes with Head Up Tilt testing as the standard test equipment in the FASS hospital based clinic.

  • REC name

    North East - Newcastle & North Tyneside 1 Research Ethics Committee

  • REC reference

    16/NE/0328

  • Date of REC Opinion

    24 Nov 2016

  • REC opinion

    Further Information Favourable Opinion