跳至主要内容
临床试验/NCT06470308
NCT06470308进行中(未招募)不适用

Prescribing Outcomes of a General Practitioner-Targeted Deprescribing Educational Intervention in Older Adults With Polypharmacy: A Cluster Randomized Trial

University of Crete1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2024年11月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
200
试验地点
1
主要终点
Potentially Inappropriate Medication

研究概览

简要总结

Polypharmacy is a common and growing public health concern across healthcare settings worldwide and is associated with an increased risk of inappropriate prescribing and adverse drug events. Deprescribing-defined as the supervised withdrawal of potentially inappropriate medications using structured tools and clinical judgment-has been proposed as a strategy to improve prescribing safety. In Greece, formal initiatives and evidence evaluating deprescribing interventions in primary care remain limited.

This study is a cluster randomized controlled trial evaluating the effect of an educational intervention for general practitioners (GPs) on prescribing safety in primary care. Participating GPs are randomized in an approximately 1:1 ratio to an intervention or control arm. GPs in the intervention arm receive structured education and training on medication review and deprescribing, including the use of validated deprescribing tools such as the Beers Criteria. GPs in the control arm provide usual care and do not receive any educational intervention.

Patients receiving care from participating GPs are recruited, and prescribing outcomes are assessed at the patient level. The primary outcome is change in prescription medications following the intervention, comparing patients cared for by GPs in the intervention arm versus those cared for by GPs in the control arm.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

  • community-dwelling patients
  • Age ≥ 65 years
  • Receive at least 5 medication ( polypharmacy )

排除标准

  • hospitalized or patients living in nursing home
  • Incapable of giving written consent

研究组 & 干预措施

Control Arm

No Intervention

No educational intervention will be provided to the general practitioners of the selected patients.

Intervention Arm

Experimental

An educational intervention and training in deprescribing algorithms and deprescribing tools ( Beers Criteria) will be provided to the general practitioners caring for the patients selected in the intervention arm.

干预措施: Medication Reviews and Deprescribing (Other)

结局指标

主要结局

Potentially Inappropriate Medication

时间窗: 1 years

Determine if there is reduction in potentially Inappropriate medication after a deprescribing education intervention

Number of medications

时间窗: 1 year

Determine if there is reduction in number of medications after a deprescribing education intervention

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Alexandros Paraskevopoulos

MD , PhD Candidate

University of Crete

研究点 (1)

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