Introducing the Palliative Care Comprehensive Tool in Family Medicine
2017年8月29日 更新者：Ainsley Moore、McMaster University
Introducing the Comprehensive Palliative Care Tool in Family Medicine : A Pilot Randomized Controlled Trial
The purpose of this study is to pilot the introduction of a newly developed palliative care tool to clinicians in a family health team.
The intent of the tool is to improve the quality and comprehensiveness of palliative care, which effects caregiver and patient satisfaction with care received, as well as clinician satisfaction with their delivery of care.
Tool effectiveness will be evaluated by measuring satisfaction scores of caregivers, patients and clinicians who receive training and access to the tool compared to caregivers, patients and clinicians providing usual care (without the tool).
Uptake of the tool and user feedback will be collected
研究概览
详细说明
A newly developed tool to guide clinicians in best palliative care practices was developed based on a combination of published tools and consultation with primary care, end users (clinicians).
The tool will be introduced as a pilot to clinicians who will receive training on use of the tool and access to the tool within a family health team in Ontario, Canada.
The tool will be applied in a controlled study environment that randomly assigns clinicians to one of two groups.
One group will receive training and access to the tool and the other group of clinicians will continue to provide usual care.The tool will be evaluated based on validated satisfaction surveys completed by caregivers, patients and clinicians.
Satisfaction scores of those randomly assigned to care enhanced by the tool will be compared to those receiving usual care at the beginning and end of the study.
Uptake of the tool will be measured, as well as user experience with the tool (feasibility and acceptability)
研究类型
介入性
注册 (预期的)
149
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习地点
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Ontario
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Hamilton、Ontario、加拿大、L8W3J6
- Stonechurch Family Health Centre, Department of Family Medicine McMaster University
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参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 及以上 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- Inclusive sample of all clinicians employed at Stonechurch Family Health Centre
- Inclusive sample of all patients over 18 years of age, registered as palliative within Stonechurch Family Health Centre and who are English speaking
Exclusion Criteria: Patients younger than 18 years of age, patients who are non-English speaking
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学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 主要用途：支持治疗
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：单身的
武器和干预
参与者组/臂 |
干预/治疗 |
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有源比较器：Palliative Care Comprehensive Tool
Clinicians within the study will be randomly assigned and trained on the use of the Palliative Care Comprehensive Tool
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Clinicians assigned to the newly developed Palliative Care Comprehensive Tool will be trained during a 1 hour period on the application of the tool; Including rationale for tool development, objective of the tool and demonstration of the tool in action
其他名称：
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无干预：Usual Care
Clinicians within the study will be randomly assigned to usual palliative care (without the newly introduced tool)
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研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
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Caregiver satisfaction
大体时间：3 months
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FAMCARE-2 survey to measure caregiver satisfaction
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3 months
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Patient satisfaction
大体时间：3 months
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FAMCARE-P13
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3 months
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Clinician satisfaction
大体时间：3 months
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Physician Satisfaction with Aspects of Chronic Care (modified)
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3 months
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User feedback
大体时间：3 months
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Acceptability and feasibility of the Palliative Care Comprehensive Tool will be sought using the Clinical Sensibility Questionnaire
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3 months
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Uptake of tool
大体时间：3 month
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Tool implementation will be (rate of tool uptake by clinician)
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3 month
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员：Ainsley Moore, MD、Department of Family Medicine McMaster University
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (预期的)
2017年9月1日
初级完成 (预期的)
2018年3月1日
研究完成 (预期的)
2018年6月1日
研究注册日期
首次提交
2017年8月29日
首先提交符合 QC 标准的
2017年8月29日
首次发布 (实际的)
2017年8月30日
研究记录更新
最后更新发布 (实际的)
2017年8月30日
上次提交的符合 QC 标准的更新
2017年8月29日
最后验证
2017年8月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.
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