Deprescribing Process in Frailty

  • Research type

    Research Study

  • Full title

    An observational Study of the Deprescribing Process in Frailty in a Falls Service and Qualitative study of Patients’ Perspective Toward This Intervention

  • IRAS ID

    331966

  • Contact name

    Anthony Cox

  • Contact email

    a.r.cox@bham.ac.uk

  • Sponsor organisation

    University of Birmingham

  • Clinicaltrials.gov Identifier

    N/A, N/A

  • Duration of Study in the UK

    1 years, 0 months, 1 days

  • Research summary

    The proposed study will evaluate deprescribing processes in frailty in current practice. In addition, it aims to explore patients’ views about this process. The study will be conducted in two phases: the quantitative phase and qualitative phase. Study period is one year. In the earlier phase (quantitative phase), observational view of frail patients in Falls service at Solihull hospital, West Midlands, will be undertaken. The required data will be extracted by the pharmacist, who is a part of medical team in Falls service and have dircet access the patients' medical record.This phase will involve analysis of anonymised data.In the late phase (qualitative phase), the patient’s perspective regarding deprescribing processes in Falls service will be qualitatively explored.
    Phases (quantitative & Qualitative) will involve the use of NHS facilities, including site, staff and patients, will be addressed.

  • REC name

    West Midlands - South Birmingham Research Ethics Committee

  • REC reference

    23/WM/0217

  • Date of REC Opinion

    21 Nov 2023

  • REC opinion

    Further Information Favourable Opinion