Interhospital Variability in Programmes to Prevent Axillary Lymphadenectomy Sequels in Breast Cancer Patients.
2018年2月22日 更新者：Violeta Pajero Otero
This study aims to determine the effectiveness of the different programmes of four Spanish hospitals about prevention of axillary lymphadenectomy sequels in breast cancer patients.
研究概览
地位
完全的
详细说明
This study aims to describe the different programs for the prevention of sequels of axillary lymphadenectomy in patients with breast cancer in four Spanish hospitals, to determine the degree of compliance of these programs and to register the frecuency of lymphedema and limitation of mobility of the upper limb in breast cancer patients undergoing axillary lymphadenectomy between 2014 and 2016 in the four hospitals.
研究类型
观察性的
注册 (实际的)
276
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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-
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Madrid、西班牙、28034
- Hospital Universitario Ramon y Cajal
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Madrid、西班牙、28041
- Hospital Universitario 12 de Octubre
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Toledo、西班牙、45071
- Castilla-La Mancha University
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Madrid
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Majadahonda、Madrid、西班牙、28222
- Hospital Universitario Puerta De Hierro
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Murcia
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Cartagena、Murcia、西班牙、30203
- Complejo Hospitalario Universitario de Cartagena
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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
女性
取样方法
概率样本
研究人群
Women suffering from axillary lymphadenectomy due to breast cancer in four spanish hospitals
描述
Inclusion Criteria:
- Suffering from axillary lymphadenectomy due to breast cancer treatment between 1 january 2014 until 31 december 2016.
Exclusion Criteria:
- Lymphedema prior to surgery in any of the upper limbs or any malformation or injury that prevents comparison of both upper limb volumes.
- Cognitive impairment or intellectual disability that would prevent understanding the instructions of the study, as well as the purpose of the same.
- Serious condition.
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
- 观测模型：病例对照
- 时间观点：追溯
队列和干预
团体/队列 |
干预/治疗 |
|---|---|
|
axillary lymphadenectomy sequels
Patients who have suffered from axillary lymphadenectomy due to breast cancer between 2014 and 2016 and who have developed breast cancer-related lymphedema and/or shoulder disability who fulfill or not a preventive programme
|
Information about risk factors for breast cancer-related lymphedema and home-based exercise programme for shoulder
No fulfillment of the preventive programme: Information about risk factors for breast cancer-related lymphedema and home-based exercise programme for shoulder
|
|
No axillary lymphadenectomy sequels
Patients who have suffered from axillary lymphadenectomy due to breast cancer between 2014 and 2016 and who have not develped breast cancer-related lymphedema and/or shoulder disability who fulfill or not a preventive programme.
|
Information about risk factors for breast cancer-related lymphedema and home-based exercise programme for shoulder
No fulfillment of the preventive programme: Information about risk factors for breast cancer-related lymphedema and home-based exercise programme for shoulder
|
|
Fulfillment of a preventive programme
Patients who fulfil a preventive programme for axillary lymphadenectomy sequels
|
|
|
No fulfillment of a preventive programme
Patients who do not fulfil a preventive programme for axillary lymphadenectomy sequels
|
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 |
|---|---|---|
|
breast cancer-related lymphedema
大体时间：The agreed date with the participant for the evaluation (second half of 2017)
|
Truncated cone formula
|
The agreed date with the participant for the evaluation (second half of 2017)
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
functional shoulder limitation
大体时间：The agreed date with the participant for the evaluation (second half of 2017)
|
Shoulder Pain and Disability Index
|
The agreed date with the participant for the evaluation (second half of 2017)
|
|
Symptoms associated with breast cancer-related lymphedema
大体时间：The agreed date with the participant for the evaluation (second half of 2017)
|
Visual Analogic Scale
|
The agreed date with the participant for the evaluation (second half of 2017)
|
其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Degree of compliance with the prevention program
大体时间：The agreed date with the participant for the evaluation (second half of 2017)
|
questionnaire
|
The agreed date with the participant for the evaluation (second half of 2017)
|
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。
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 (实际的)
2017年9月27日
初级完成 (实际的)
2017年12月31日
研究完成 (实际的)
2017年12月31日
研究注册日期
首次提交
2017年9月28日
首先提交符合 QC 标准的
2017年9月28日
首次发布 (实际的)
2017年10月3日
研究记录更新
最后更新发布 (实际的)
2018年2月23日
上次提交的符合 QC 标准的更新
2018年2月22日
最后验证
2018年2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.