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Published on: August 1, 2019
Implementation of a hospital deprescribing behaviour change intervention, the CompreHensive geriAtRician-led
Jacqueline M Martin-Kerry1, Debi Bhattacharya2, Johanna Taylor3
1School of Health Sciences, University of East Anglia, Norwich, UK jackie.martin-kerry@uea.ac.uk.
Insights
This study evaluated the CHARMER intervention to increase proactive deprescribing in hospitals. The CHARMER trial used a stepped-wedge design to assess its effectiveness and cost-effectiveness in improving medication management.
Area of Science:
- Geriatric Medicine
- Pharmacology
- Health Services Research
Background:
- Proactive deprescribing involves four steps: identifying, evaluating, stopping, and monitoring medication cessation.
- The CHARMER (CompreHensive geriAtRician-led MEdication Review) trial is a stepped-wedge study assessing a behavior change intervention for proactive deprescribing in hospitals.
- The CHARMER intervention includes an action plan, briefings, case studies, videos, and a performance dashboard to facilitate deprescribing.
Purpose of the Study:
- To evaluate the effectiveness and cost-effectiveness of the CHARMER intervention in increasing proactive deprescribing.
- To explore the implementation processes, behavioral mechanisms, and contextual factors influencing the CHARMER intervention through a process evaluation.
Main Methods:
- A convergent parallel design process evaluation guided by UK Medical Research Council standards.
- Interviews with healthcare staff, patients/carers, and primary care practitioners, supplemented by implementation activity recordings and manuals.
- Quantitative data from questionnaires on deprescribing steps and behavioral mechanisms, analyzed descriptively and with Mann-Whitney tests; qualitative data thematically analyzed and mapped to Normalization Process Theory and Theoretical Domains Framework.
Main Results:
- The study is designed to capture the extent to which the four proactive deprescribing steps are enacted.
- It aims to measure the behavioral mechanisms driving the CHARMER intervention's effects.
- Patient experiences with proactive deprescribing will be assessed.
Conclusions:
- The CHARMER trial aims to provide evidence on the effectiveness and cost-effectiveness of a comprehensive deprescribing intervention.
- The process evaluation will offer insights into successful implementation strategies and barriers.
- Findings will inform future deprescribing initiatives in hospital settings.
Introduction:
Proactive deprescribing is the process of stopping a medicine and comprises four steps: (1) identify a patient for potential stop of a medicine, (2) evaluate a patient for potential stop of a medicine, (3) stop a medicine and (4) monitor after stopping.The CHARMER (CompreHensive geriAtRician-led MEdication Review) trial is a stepped-wedge design to evaluate the effectiveness and cost-effectiveness of a behaviour change intervention to increase proactive deprescribing in hospitals. The CHARMER intervention comprises a deprescribing action plan, deprescribing briefings, videos of successful deprescribing consultations, deprescribing case studies workshop and a deprescribing performance dashboard. The process evaluation will explore trial processes, CHARMER intervention implementation, CHARMER behavioural mechanisms of action and contextual factors influencing these aspects.
Methods And Analysis:
The convergent parallel design process evaluation will follow the UK Medical Research Council guidance. We will interview: staff involved in CHARMER implementation, geriatricians and pharmacists who receive the intervention and research delivery staff involved in patient/carer recruitment and data collection. We will also interview patients/carers and primary care practitioners. Interviews will be supplemented with recordings of implementation activities and completed implementation manuals. Questionnaires will capture the extent to which the four proactive deprescribing steps are enacted by intervention recipients, measure the behavioural mechanisms by which the CHARMER intervention operates and capture the patient experience of proactive deprescribing. Qualitative data will be analysed thematically and then mapped to Normalisation Process Theory to explore implementation and the Theoretical Domains Framework to explore behaviour change. Most quantitative data will be analysed descriptively; however, changes in staff questionnaire responses preintervention and postintervention will be analysed using a Mann-Whitney test. We will triangulate qualitative and quantitative findings to explain intervention effects.
Ethics And Dissemination:
Ethical and governance approvals have been obtained by the Wales 2 Research Ethics Committee and the Health Research Authority, respectively. The dissemination strategy will be underpinned by the evidence-based Guide to Disseminating Research (GuiDiR) targeting healthcare practitioners, policy makers and patient-facing organisations.
Trial Registration Number:
ISRCTN13248281.
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