The MyAction LifeNote study

  • Research type

    Research Study

  • Full title

    To evaluate the role of LifeNote in rates of medicine adherence and also its acceptability in patients at high multifactorial risk of developing cardiovascular disease attending the MyAction Westminster programme

  • IRAS ID

    131456

  • Contact name

    SB Connolly

  • Contact email

    s.connolly@imperial.ac.uk

  • Sponsor organisation

    Joint Research Compliance Office

  • Research summary

    Achieving desirable blood pressure and cholesterol levels in every day clinical practice is far from ideal. There are many reasons for this but an important one is patient’s not adhering to their medication. This includes taking it at the wrong time, missing doses or stopping it altogether. This results in an increased risk of heart disease/stroke in the longer term. Effective strategies that help patients adhere better to their medication are still lacking. Such strategies are urgently needed to help improvement not just in the prevention of heart disease/stroke but also in other areas of chronic disease management.
    LifeNote is a system which permits a patient to monitor taking his medication electronically. Alongside his/her usual medication, the patient also ingests a LifeNote pill. Once this comes in contact with the stomach acid, it emits a signal to a sensor patch the patient wears on his/her skin. This is then transmitted by bluetooth technology to a tablet device where the patient can see his/her medication taking schedule. The system also includes the capability for sending reminder text messages if the patient does not take his medication at the correct time.
    We want to explore this device in 20 patients attending a community-based vascular prevention programme specifically in those already taking blood pressure or cholesterol lowering medication. We want to examine how adherent patient are to their medication whilst using the LifeNote system and we also want to examine how patients feel about using the device (i.e. is acceptable/useful in their opinion? etc). The patients will use the system for the duration of the MyAction programme which typically lasts about 12 weeks.

  • REC name

    London - Surrey Borders Research Ethics Committee

  • REC reference

    13/LO/1279

  • Date of REC Opinion

    10 Sep 2013

  • REC opinion

    Further Information Favourable Opinion