跳至主要内容
临床试验/NCT04889794
NCT04889794招募中不适用

GPS Project - Evaluation of the Impact of the Reorganization of Work Into a Family Medicine Group on Pharmacotherapy and Support for the Autonomy of Seniors With Major Neurocognitive Disorders

CHU de Quebec-Universite Laval2 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2021年9月27日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
400
试验地点
2
主要终点
Change in number of prescribed medications

研究概览

简要总结

The model of care tested in the GPS project aims to optimize pharmacotherapy for seniors undergoing cognitive assessment or suffering from major neurocognitive disorder (MCND) at home. The goal is to reduce polymedication, inappropriate medications and the treatment burden of seniors and to maintain their cognitive health, quality of life and autonomy. The intervention will include knowledge exchange sessions with nurses, pharmacists, and doctors in FMGs, and increased collaboration between these professionals and home care services teams. Other goal is to increase the satisfaction of the seniors, their families, and the professionals involved in the GPS project.

详细描述

: The GPS project is part of the desire to keep seniors with major neurocognitive disorder (MCND) in their homes for as long as possible. Medication can contribute to cognitive loss in seniors and affect their functional autonomy. The arrival of pharmacists in FMGs and the expansion of their practice is opening up new opportunities to promote interdisciplinary collaboration and optimize pharmacotherapy for seniors. During the project, a new model of care, called GPS, is being tested with seniors. A group of seniors (approximately 200) will receive the new care team's new interventions in the FMGs in the "intervention" group. Another group of seniors (about 200) will receive the usual care in other FMGs that will serve as a "control" group. By comparing the results of the two groups, it will be possible to evaluate the effects of new interventions. A period of 12 months will be allocated for the inclusion of seniors. The follow-up of each senior will be approximately 6 months.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Health Services Research
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
否

入选标准

  • •All seniors (65 years of age or older) undergoing cognitive evaluation OR referred to a memory clinic OR having been diagnosed with cognitive impairment within the last year OR with MCND and followed up at home AND,
  • •referred to the pharmacist, for the FMGs exposed
  • •taking prescription medications

排除标准

  • •Seniors in palliative care OR
  • •unable to answer questionnaires in French AND without a caregiver.

研究组 & 干预措施

Exposed FMGs to GPS intervention

Experimental

Patients who are followed by FMGs exposed to the GPS intervention. They will receive the GPS intervention.

干预措施: GPS clinical intervention (Other)

Non exposed FMGs to GPS intervention

No Intervention

Patients who are part of the FMGs not exposed to the GPS intervention. They will receive the usual care and services.

结局指标

主要结局

Change in number of prescribed medications

时间窗: Baseline, 3 months and 6 months after inclusion in the study.

The total number of prescribed medications and 2) the number of potentially inappropriate medications (PIMs) according to the Beers criteria or according to the OptimaMed criteria for participants with advanced MCND will be measured in both groups, before, during and after the study.

次要结局

  • Change in treatment burden(Baseline and 6 months follow-up)

研究者

发起方
CHU de Quebec-Universite Laval
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dre Edeltraut Kröger

Professor

CHU de Quebec-Universite Laval

研究点 (2)

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