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临床试验/NCT02979353
NCT02979353已完成不适用

A Randomized Controlled Trial to Deprescribe for Older Patients With Polypharmacy Transferred From the Hospital to Skilled Nursing Facilities

Vanderbilt University Medical Center2 个研究点 分布在 1 个国家目标入组 372 人开始时间: 2017年3月6日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
372
试验地点
2
主要终点
Total Number of Medications

研究概览

简要总结

This randomized, controlled trial will evaluate the effects of an intervention to reduce exposure to medications among hospitalized older adults discharged to skilled nursing facilities (SNFs). The goal of the intervention is to safely deprescribe medications, as defined by dose reductions and stopped medications, based on a combination of clinical criteria and patient preferences. The investigators will evaluate the effects of the intervention on the total number of medications prescribed to patients at hospital and SNF discharge and at home 90-days after SNF discharge along with the prevalence of eight geriatric syndromes, medication adherence, and health status.

详细描述

This randomized, controlled trial will evaluate the effects of an intervention to reduce exposure to medications among hospitalized older adults discharged to skilled nursing facilities (SNFs). This study will be conducted in one university-affiliated hospital and 14 area SNFs to enroll approximately 1,300 total participants across five project years. Patients discharged to SNF represent the largest segment of Medicare beneficiaries discharged to post-acute care services and are a particularly high risk group for loss of independence and other poor clinical outcomes. This investigative team recently completed a Centers for Medicare and Medicaid Services (CMS) Innovation Award, which provides strong preliminary data related to the prevalence of polypharmacy and the relationship between polypharmacy and geriatric syndromes (e.g., medications associated with falls) in this patient population. Based on these data, the investigators developed a structured deprescribing intervention protocol ("Shed-Meds") coupled with standardized screening assessments for eight geriatric syndromes to be implemented in the hospital and continued during the SNF stay. The goal of the intervention is to safely deprescribe medications, as defined by dose reductions and stopped medications, based on a combination of clinical criteria and patient preferences. This trial will evaluate the effects of this intervention on medication exposure, medication adherence, geriatric syndromes, and health status across the care transitions from hospital to SNF to home to include a 90-day follow-up period after SNF discharge. The overarching hypothesis is that reducing medications for older patients across the continuum of care will favorably impact geriatric syndromes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Hospitalized at Vanderbilt University Medical Center
  • Medicare-eligible
  • Discharged from VUMC to a post acute care facility
  • Has polypharmacy as defined by > 5 medications
  • Able to self-consent or has a proxy (surrogate)
  • Speaks English (due to interview-based assessments)
  • Primary home residence within one of 9 surrounding counties (due to home visit during follow-up phase)

排除标准

  • Resides in long-term care
  • Is currently on hospice or otherwise has a limited life expectancy (< 6 months).
  • Enrolled in a clinical drug trial
  • Has Stage IV Cancer Diagnosis
  • Incarcerated or homeless
  • Unable to self-consent and does not have a surrogate

结局指标

主要结局

Total Number of Medications

时间窗: Hospital Discharge, Post-Acute Care Discharge, and 90 days after discharge from the PAC

The number of medications a participant is taking. This includes all prescribed and over-the-counter medications and both scheduled and as-needed (PRN) medications.

次要结局

  • Total Drug Burden Index (DBI): Anticholinergic and Sedative Drug(Hospital Discharge, Post-Acute Care Discharge, and 90 days after discharge from PAC)

研究者

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

Sandra Simmons

Principal Investigator

Vanderbilt University Medical Center

研究点 (2)

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