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临床试验/NCT01876095
NCT01876095已完成不适用

Discontinuing Inappropriate Medication in Nursing Home Residents (the DIM NHR Study): a Cluster Randomized Controlled Trial

University of Groningen2 个研究点 分布在 1 个国家目标入组 992 人开始时间: 2014年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
992
试验地点
2
主要终点
Successful medication discontinuation

研究概览

简要总结

Nursing home residents are among the frailest patient groups with a high number of co-morbidities and a high use of medicines. Inappropriate polypharmacy (i.e. often overprescribing) is one of the major problems in the nursing home population increasing the number of adverse drug reactions, falls, hospital admissions, mortality as well as having an impact on health care utilization. Multidisciplinary medication reviews have a great potential to reduce inappropriate medication use. The purpose of this study is to determine the efficacy of a multidisciplinary medication review model focussing on discontinuing inappropriate medication in a cluster randomized controlled trial in 600 nursing home residents. The primary outcome measure is the difference in proportion of residents who successfully discontinued medication between intervention and control group after four months. Secondary outcome measures will be the drug burden index, adverse drug withdrawal events related to the discontinued medication, death, referral to hospitals and quality of life.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Participant, Outcomes Assessor)

入排标准

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

Successful medication discontinuation

时间窗: 4 months

The number of residents for whom ≥1 inappropriate medication(s) are succesfully discontinued i.e. without relapse or severe withdrawal effects

次要结局

  • Dose adjustment(4 months)
  • Death(4 months)
  • Safer alternative medication(4 months)
  • Bone fractures(4 months)
  • Drug burden index(4 months)
  • Quality of Life(4 months)
  • adverse drug withdrawal events(4 months)
  • Hospital admission(4 months)
  • Falling(4 months)
  • number of visits to outpatient clinics / emergency rooms / by medical consultants(4 months)
  • Medication initiation(4 months)

研究者

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

Katja Taxis

Professor of Pharmacotherapy and Clinical Pharmacy

University of Groningen

研究点 (2)

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