Living With Cervical Cancer: Assessing Utilities Associated With Common Treatment Complications
研究概览
地位
条件
研究类型
注册 (实际的)
联系人和位置
学习地点
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Wisconsin
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Madison、Wisconsin、美国、53792
- University of Wisconsin-Madison
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
Patient Population: Patients ≥18 and <61 years old who were diagnosed with early cervical cancer (stages I and II) at least 3 years prior to the interview. We cannot limit our population to stage IB2 patients and meet our accrual goals due to the rarity of the disease. Patients with stages I and II cervical cancer are included because they have the potential to be exposed to the same treatment complications as patients with stage IB2 disease. Patients of all health statuses will be accepted.
Provider Population: Providers who care for patients with cervical cancer at the University of Wisconsin, including: gynecologic oncologists, radiation oncologists, physician's assistants and nurses. Providers must be ≥18 and <61 years old in any health status.
描述
Inclusion Criteria:
- A subject has to have been diagnosed with early cervical cancer (Stage I or II) within the last 3 years and/or take care of patients with cervical cancer and identify her or himself as one of the following: gynecologic oncologist, radiation oncologist, physician's assistant or nurse.
- Subjects must be ≥18 and <61 years old.
Exclusion Criteria:
- Subjects who are unable to read and speak English proficiently will be excluded. Proficiency will be assessed by the investigator enrolling patients.
- Subjects who do not have capacity to consent will not be included in this study.
- Subjects may not be investigators on this study.
学习计划
研究是如何设计的?
设计细节
- 时间观点:横截面
队列和干预
团体/队列 |
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病人
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Providers
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
---|---|
Utilities of complications associated with cervical cancer treatment.
大体时间:At time of interview
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At time of interview
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合作者和调查者
调查人员
- 首席研究员:Ellen M Hartenbach, MD、University of Wisconsin, Madison
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
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.