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临床试验/ISRCTN30626972
ISRCTN30626972已完成未知

A feasibility study to determine the effectiveness and cost effectiveness of medication organisation devices in facilitating health benefit and medication adherence in a population aged 75 years and over and taking three or more solid oral dose form medications compared to usual care which will inform future trial design.

niversity of East Anglia (UK)0 个研究点目标入组 120 人开始时间: 2012年4月23日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Aged 75 years or over
  • 2. Are prescribed three or more solid oral dose form medications for the management of a chronic condition
  • 3. Have a life expectancy equal to or in excess of one year
  • 4. Are capable of providing informed consent

排除标准

  • 1. Participants in receipt of a prescribed medication organisation device or with a history of having received amedication organisation device
  • 2. Are resident in a care home
  • 3. Are currently or have recently been involved in medication intervention trials
  • 4. Have been diagnosed with Parkinson's disease
  • 5. Have a severe mental health disorder such as schizophrenia or other clinical contraindications which in the opinion of the healthcare team renders the patient inappropriate for trial participation

研究者

发起方
niversity of East Anglia (UK)

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