跳至主要内容
临床试验/NCT05705284
NCT05705284招募中不适用

The Development and iMplementation Of a Multidisciplinary Medication Review and Deprescribing Intervention Among Frail Older People in primarY Care (MODIFY Study)

University of Southampton1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2022年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
90
试验地点
1
主要终点
Number of medications

研究概览

简要总结

A third of older people take five or more regular medications (polypharmacy) potentially increasing the risk of side-effects, hospital admission and death, with higher risk among people living with frailty. National recommendations suggest that medications taken by frail older people should be reviewed annually by GPs to identify and reduce/ stop inappropriate medications (deprescribing). Yet this does not happen routinely due to GPs' lack of time, increased workloads and worries about stopping medicines. Recent recommendations suggest involving other non-medical prescribers such as practice-pharmacists and advanced nurse practitioners (ANPs) in reviewing medications. However, it is unknown how staff could work together most effectively and whether they have any training needs.

This research will investigate how practice-pharmacists, ANPs and GPs could best work together with patients living with frailty to perform regular medication reviews. There are four work packages (WPs).

  1. Review literature to identify what makes a successful medication review and how to safely deprescribe.
  2. Interviews with GPs, practice-pharmacists, ANPs, frail older patients and carers will investigate where medication review should take place, the role of involved parties, type of medications that could be deprescribed, staff training needs, barriers and facilitators for implementation, and strategies to address them.
  3. Information from WP1&2 will be used to develop the intervention: a structured medication review process using pharmacists, ANPs and GPs and involving frail patients and their families in decisions about medications. This will be refined through workshops with service users, clinicians and commissioners. A training programme to implement the intervention and increase staff confidence in deprescribing will be developed alongside the intervention.
  4. Feasibility study for staff in four GP practices to be trained and to implement the intervention.(this will be subject to further amendment).

详细描述

Background A third of older people take five or more regular medications (polypharmacy) potentially increasing the risk of side-effects, hospital admission and death. These effects are higher among people living with frailty who lose their in-built reserves and become vulnerable to changes triggered by small events such as a change in medication. National recommendations suggest that medications taken by frail older people should be reviewed annually by their GPs to identify and reduce/ stop inappropriate medications (deprescribing). Yet this does not happen routinely due to GPs' lack of time, increased workloads and worries about stopping medicines.

Recent recommendations suggest involving other non-medical prescribers such as practice-pharmacists and advanced nurse practitioners (ANPs) in reviewing medications. However, it is unknown how staff could work together most effectively and whether they have any training needs.

Aim This research will investigate how practice-pharmacists, ANPs and GPs could best work together with patients living with frailty to perform regular medication review.

Methods The study involves four work packages (WPs). The research team will review previous literature to identify what makes a successful medication review and how to safely reduce/ stop inappropriate medications (WP1).

Interviews with GPs, practice-pharmacists, ANPs, frail older patients and carers will be conducted (WP2). These will discover views about where medication review should take place, the role of each of the involved parties in the process, type of medications that could be deprescribed, staff development and training needs, barriers and facilitators for implementation, and strategies to address these barriers.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Number of medications

时间窗: change in scores between baseline and 3 months follow up

Total number of medications taken by each patient

Mortality rates

时间窗: 3 months

mortality rates 3 months post intervention

Feasibility of recruitment

时间窗: Baseline

proportion of staff recruited and trained in each GP practice

Rates of fractures

时间窗: changes between baseline and 3 months

number of fractures and proportion of people sustained fractures (self-reported)

Feasibility of deprescribing

时间窗: 3 months follow up

number of recommendations in the medication reviews made to each patient (stop, reduce, switch or start).

number of potentially inappropriate medications

时间窗: Change between baseline and 3 months follow up

total number of potentially inappropriate medications months using the STOPP/START criteria.

frailty status

时间窗: changes between baseline and 3 months

Frailty score using the electronic frailty index (e-FI)

rates of falls

时间窗: changes between baseline and 3 months

number of falls reported and proportion of fallers (self-reported)

function

时间窗: changes between baseline and 3 months

Activity of daily living using Barthel

Rates of adverse events

时间窗: at 3 months

rates of adverse drug events due to deprescribing (including self-reported dizziness, falls, drowsiness, confusion, hallucinations, blurred vision, constipation, diarrhoea, dry mouth or other) during 3 months follow up.

Rates of hospitalisation

时间窗: 3 months

rates of hospitalisation 3 months post intervention

healthcare utilisation

时间窗: at 3 months follow up

number of visits to GP/specialists and number of unplanned hospitalisations

Acceptability

时间窗: at 3 months follow up

Interviews or focus groups will be conducted at the end of the feasibility study with a purposive sample of (n=6-8) GPs, pharmacists, ANPs in the four GP practices who received the training and implemented the intervention, and 8-10 patients and carers who received the intervention

cognition

时间窗: changes between baseline and 3 months

\- cognition using the abbreviated mental test (AMT)

depression

时间窗: changes between baseline and 3 months

\- depression using the geriatric depression scale (GDS)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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MODIFY or Medication Review in Primary Care Study | 临床试验