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临床试验/NCT01504672
NCT01504672已完成不适用

A Randomized Controlled Pharmacist Intervention Study to Reduce Drug-related Problems and Readmissions Among Old People With Dementia

Umeå University2 个研究点 分布在 1 个国家目标入组 460 人开始时间: 2012年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
460
试验地点
2
主要终点
Number of Patients Readmitted Because of Drug Related Reasons

研究概览

简要总结

The aim of this randomized controlled study is to investigate if medication reviews performed by a clinical pharmacist as part of a ward team can reduce drug related problems and reduce readmissions to hospital among elderly patients (≥65 years) with dementia and cognitive failure.

Four hundred and sixty patients will be recruited and randomized to control (usual care) and intervention group (enhanced service in which a pharmacist is part of the health care team).

Six months after the last patient of the 460 has been discharged the study will be closed. Data about the number of readmissions and visits to the emergency room will be collected during the six-month follow-up and also, the costs associated with each visit or admission. Time until institutionalization will be compared between intervention group and control group.

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
Single (Outcomes Assessor)

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

  • Patients with dementia or cognitive impairment
  • Patients ≥ 65 years

排除标准

  • Patients previously admitted to the study wards during the study period

研究组 & 干预措施

Usual care

No Intervention

Medication review

Experimental

干预措施: Medication review (Other)

结局指标

主要结局

Number of Patients Readmitted Because of Drug Related Reasons

时间窗: Six months follow-up

次要结局

  • Frequency of Emergency Department Visits During the 6-month Follow-up.(Six months follow-up)
  • Change in the Number of Participants With Potentially Inappropriate Medications, According to the Swedish National Board of Health and Welfare, at Admission and Discharge Between Intervention and Control Group(Index admission (at randomization) and index discharge (duration of index admission, mean days 8.7))
  • Cost for Visits for Readmissions and to the Emergency Department Compared Between Patients in the Control Group and Intervention Group.(Six months follow-up)
  • Number of Participants Institutionalized After Discharge, in Control Group and Intervention Group.(Six months follow-up)

研究者

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

Hugo Lovheim

Principal Investigator

Umeå University

研究点 (2)

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