Benefit and Risk Information for Medication in Multiple Sclerosis (1)

  • Research type

    Research Study

  • Full title

    Improving understanding and recall of risk information relating to MS medication: Developing an evidence-based clinical tool for assisting communication and understanding of MS medication risk information between patients and health professionals - Benefit and Risk information for Medication in Multiple Sclerosis (BRIMMS)

  • IRAS ID

    155057

  • Contact name

    Gurpreet Reen

  • Contact email

    Gurpreet.reen.2014@live.rhul.ac.uk

  • Sponsor organisation

    Royal Holloway, University of London

  • Research summary

    We propose to develop an evidence-based clinical tool for patients which would support communication and understanding of medication risk information in Multiple Sclerosis (MS). The new and emerging medications in MS offer varying risk-benefit profiles which are not always correctly interpreted and understood by patients, with research showing a difference in risk awareness between patients and health professionals. This is especially significant when treatments have higher efficacy but potentially serious risks such as that of Natalizumab, a drug given to patients with Relapsing Remitting Multiple Sclerosis (RRMS).
    The present research will focus on risk-benefit profiles of medications and treatments of RRMS patients recruited from King’s College Hospital and Lewisham and Greenwich NHS Trust, where the study is expected to be conducted. Firstly, interviews and questionnaires with patients will indicate current risk and benefit understanding of medications. Health professionals will also be surveyed to provide an indication of current clinical information needs. Secondly, three experiments will be conducted with patients to evaluate the efficacy of different presentation formats, different organisational patterns of information and different strategies for supporting understanding and recall of health information. Previous research and the findings across these stages will be integrated and further amended with feedback from patients and professionals, to ultimately produce a generic protocol to be used with current risk and benefit information relating to any disease-modifying drug, known as the Benefit and Risk Information for Medication in Multiple Sclerosis (BRIMMS) protocol.

  • REC name

    South Central - Oxford C Research Ethics Committee

  • REC reference

    14/SC/1266

  • Date of REC Opinion

    23 Sep 2014

  • REC opinion

    Further Information Favourable Opinion