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临床试验/NCT02299180
NCT02299180已完成不适用

Impact of Advance Care Planning on Care for Patients With Advanced Heart Failure: A Randomized Controlled Trial

Duke-NUS Graduate Medical School4 个研究点 分布在 1 个国家目标入组 282 人开始时间: 2015年2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
发起方
入组人数
282
试验地点
4
主要终点
Proportion of patients receiving end of life care consistent with their stated preferences

研究概览

简要总结

Aims: Advance care planning (ACP) is considered to be one of the most promising interventions to enable patients with life limiting illnesses to receive treatment at the end of life (EOL) according to their own preferences and to promote EOL conversations between patients and their health care providers. Through a 2-arm randomized controlled trial (RCT) of patients with Class III and IV heart failure (New York Heart Association Functional Classification), we propose to assess:

  1. Whether patients in the ACP arm have a greater likelihood of receiving EOL care consistent with their preferences as stated in the latter of the last ACP document or the last patient interview, compared to patients in the control arm.
  2. Heath care costs during study duration between patients in ACP and control arms.
  3. Patient's understanding of own illness and their participation in decision making between the ACP and control arms.
  4. Patient's quality of life, anxiety and depression between ACP and control arms.

Methodology: A total of 254 patients with advance heart failure will be randomized to receive intervention (ACP arm; N=127) or usual care (control arm; N=127).

The RCT will be conducted at the National Heart Centre and Singapore General Hospital. Patients in both arms will be followed for one year or till death, whichever is earlier, and interviewed every 4 months during this duration.

Clinical Significance: If benefits of ACP are shown to add value through this trial, then this study will help to promote acceptance of ACP among patients and health care providers across Singapore and elsewhere.

研究设计

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

入排标准

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

入选标准

  • Patient participant:
  • Patients must be 21 years old or older and must be diagnosed with advanced heart failure (New York Heart Association Class III and IV). Patients must be aware of their diagnosis
  • Caregiver/Decision-maker participant: Subject must be 21 years old or older Participant must be either
  • appointed substitute decision maker or
  • most likely to be substitute decision maker for patient (if patient were to lose decision-making capacity)

排除标准

  • Patient participant: Patients must not have any psychiatric or cognitive disorders
  • Caregiver/Decision-maker participant: Cannot be a maid or foreign domestic worker

研究组 & 干预措施

Control arm

No Intervention

The control arm patients will not take part in ACP discussions and documentation, but will continue to receive usual care.

Intervention (ACP) arm

Experimental

The patient and his/her family members will be referred to an ACP facilitator and will undergo ACP as an ongoing process, integrated with patient's care, from the facilitator, in coordination with a coordinator/nurse, and treating physician. The ACP facilitator will be certified in providing ACP and will possess sufficient knowledge of the risks, benefits, and harms of treatments and procedures available to the patient. The ACP facilitator will be supported by the physician with the specialized knowledge of treatment options, especially with regards to prognosis. Family members will be encouraged to be present during the ACP discussion so that the whole family unit will be able to explore goals, values and beliefs towards the patient's medical care.

干预措施: ACP (Behavioral)

结局指标

主要结局

Proportion of patients receiving end of life care consistent with their stated preferences

时间窗: one year

Patient's stated preferences for cardiopulmonary resuscitation (CPR) and life prolonging treatments (e.g. mechanical ventilation, dialysis, feeding tube, intravenous antibiotics, blood transfusion) will be assessed from their last survey or their ACP document. The actual treatment received by the patient will be assessed from medical records after the patient's death. Proportion of patients who died and received treatment consistent with their stated preferences will be calculated and compared between ACP and control arms

次要结局

  • Total health care expenditure of patients during study duration(one year)
  • Patient scores for anxiety and depression(every four months for one year)
  • Patient's participation in decision-making(every four months for one year)
  • Patient's understanding of own illness(every four months for one year)
  • Patient scores for Quality of life(every four months for one year)

研究者

发起方
Duke-NUS Graduate Medical School
申办方类型
Other
责任方
Principal Investigator
主要研究者

Chetna Malhotra

Assistant Professor

Duke-NUS Graduate Medical School

研究点 (4)

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