跳至主要内容
临床试验/NCT00234286
NCT00234286已完成不适用

Intervention to Improve Care at Life's End in VA Medical Centers

US Department of Veterans Affairs2 个研究点 分布在 1 个国家目标入组 78 人开始时间: 2005年8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
78
试验地点
2
主要终点
Presence of Order for Opioid Pain Medication

研究概览

简要总结

The BEACON trial (Best Practices for End-of-Life Care for Our Nations' Veterans) was a six-site implementation study to evaluate a multi-component, education-based intervention to improve the quality of end-of-life care provided in VA Medical Centers.

详细描述

The BEACON trial (Best Practices for End-of-Life Care for Our Nations' Veterans) was a six-site, real-world implementation trial of a multi-component, education-based intervention to improve the quality of end-of-life care conducted in VA Medical Centers (VAMCs).

The primary aim was to evaluate the effectiveness of a multi-component intervention for improving processes of care provided in the last days of life in VAMCs. The second aim was to conduct after-death interviews with next-of-kin and qualitative analysis of their perceptions of the care provided to the veteran and family.

The multi-component intervention targeted VAMC inpatient providers, including physician, nursing, and ancillary staff. It consisted of preparatory site visits, a staff training program, a newly developed Comfort Care order set decision support tool built into the CPRS, and follow-up consultation. The intervention team travelled to each site to conduct two weeks of comprehensive in-service training. Staff were trained to identify actively-dying patients and implement a set of best practices of traditionally home-based hospice care for dying patients. The team provided assistance with policies, procedures, and skill training needed to implement comfort care interventions. Introduction of the intervention at each VAMC was staggered across time at six-month intervals using a multiple-baseline, stepped wedge design.

Data on processes of end-of-life care (last 7 days) were abstracted from the CPRS medical records of all veterans who died before, during, and after the intervention (January 2005-February 2011). A priori, five processes of care were identified as primary endpoints to indicate quality of end-of-life care: 1) presence of an order for opioid pain medication at time of death; 2) a do-not-resuscitate (DNR) order in place at time of death; 3) location of death; 4) presence of enteral feeding tube or intravenous line at time of death; and 5) physical restraints in place at or near time of death.

In addition, in-depth, face-to-face interviews were conducted with 78 bereaved next-of-kin.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Aim 1: Not applicable. Patients were deceased.
  • Aim 2: After-death interviews with next of kin: must be willing and able to participate in after-death interview at local VA Medical Center.

排除标准

  • 未提供

结局指标

主要结局

Presence of Order for Opioid Pain Medication

时间窗: Pre and Post Intervention

Presence of order for opioid pain medication at time of death based on abstraction of electronic medical record

次要结局

  • Number of Patients Who Died in ICU(Pre and Post Intervention)
  • Individuals Administered of Opioid Medication(Pre and Post Intervention)
  • Individuals With Pastoral Care Visit(Pre and Post Intervention)
  • Individuals With a Palliative Care Consultation(Pre and Post Intervention)
  • Do Not Resuscitate Order(Pre and Post Intervention)
  • Individuals With a Nasogastric Tube(Pre and Post Intervention)
  • Individuals With an Intravenous Line(Pre and Post Intervention)
  • Number of Individuals Who Died in Restraints(Pre and Post Intervention)
  • Individuals With an Order for Benzodiazepine Medication(Pre and Post Intervention)
  • Individuals Who Received Benzodiazepine Medication(Pre and Post Intervention)
  • Individuals With an Advance Directive(Pre and Post Intervention)
  • Individuals With an Order for Antipsychotic Medication(Pre and Post Intervention)
  • Sublingual Administration(Pre and Post Intervention)
  • Individuals Administered Antipsychotic Medication(Pre and Post Intervention)
  • Individuals Who Received Scopolamine(Pre and Post Intervention)

研究者

申办方类型
Fed
责任方
Sponsor

研究点 (2)

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