跳至主要内容
临床试验/NCT02398617
NCT02398617撤回不适用

Facilitating End-Of-Life Decision Making and Preparedness Planning Among Heart Failure Patients Hospitalized for Advanced Disease

Saint Luke's Health System2 个研究点 分布在 1 个国家开始时间: 2014年12月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
2
主要终点
Kansas City Cardiomyopathy Questionnaire (KCCQ)

研究概览

简要总结

Heart failure is a chronic and frequently terminal illness associated with poor quality of life and high burden of morbidity, re-hospitalization, and cost. Accordingly, recent guideline updates have highlighted the need for improved focus on end-of-life and palliative care of advanced heart failure patients, in whom symptom burden can be high and treatment options are often limited. The aims of this study are to evaluate the feasibility of implementing a semi-structured, outpatient, nurse practitioner-led, educational supportive care intervention concerning multiple domains of end-of-life care not often included in regular, outpatient clinic visits.

详细描述

This study will be a prospective pilot enrolling 10 patients with advanced disease admitted to the heart failure service at St. Luke's Mid America Heart Institute and who are not candidates for advanced therapies such as heart transplant or mechanical circulatory support (left ventricular assist device). Potential enrollees will be identified using a validated risk model that predicts death or poor quality of life in the six months after discharge from the hospital for heart failure exacerbation. Enrolled patients will complete validated questionnaires while still hospitalized, regarding health-related quality of life, illness acceptance, prioritization of different life goals, and confidence in decision-making regarding their terminal heart failure. Patients will then be given a paper exercise regarding delineation of an end-of-life plan and appointment of a surrogate medical decision-maker, to be completed after discharge. At their regularly scheduled admission follow-up visit with seven days of discharge, participants will be asked to bring their medical decision maker and participate in a semi-structured supplemental palliative care/education session facilitated by a heart failure nurse practitioner trained in palliative care discussions. Domains included in the intervention will include disease literacy and understanding, goals of care, legal issues for patients with terminal illness, symptom management, health-related quality of life, caregiver burden, patient autonomy, healthcare utilization, and establishment of end-of-life plans.

Outcomes to be measured after the intervention include repeated validated questionnaires and unstructured patient interviews at 1 month and, at 6 months, creation of a formalized end-of-life plan, change in code status, obtainment of an advanced directive, designation of a durable power of attorney, frequency of re-hospitalizations, emergency room visits and unscheduled clinic visits with providers, and death. These will be obtained at the time of regularly scheduled heart failure clinic follow-up visits or over the phone.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

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

入选标准

  • advanced heart failure
  • ineligible for advanced therapies
  • 50% risk of death or continued poor heart failure-related health status at 6 months from hospital discharge, based on validated risk score

排除标准

  • Hospice enrollment
  • Previous heart transplant or left ventricular assist device placement

结局指标

主要结局

Kansas City Cardiomyopathy Questionnaire (KCCQ)

时间窗: 1 month

Heart failure-related quality of life

Decisional Conflict Scale

时间窗: 1 month

Decision-making confidence/readiness

Peace, Equanimity, and Acceptance in Cancer Experience (PEACE) Scale

时间窗: 1 month

Illness Acceptance

Kaldjian's Goals of Care at End of Life

时间窗: 1 month

Patient-ranked importance for different goals of care

次要结局

  • Death(6 months)
  • Code Status Change(6 months)
  • Advance Directive creation(6 months)
  • Durable Power of Attorney appointment(6 months)
  • Unscheduled Healthcare Encounter(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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