Online Study of Colorectal Cancer and Prostate Cancer Screening Decision Making (CARR2)
2017年4月21日 更新者：University of North Carolina, Chapel Hill
A Comparison of the Effect of a Conjoint Analysis Based Values Clarification Exercise, Rating and Ranking Exercise, and Balance Sheet for Colorectal Cancer Screening and Prostate Cancer Screening Decision Making
Participants will be recruited from the United States and Australia to take an online survey about colon cancer screening or prostate cancer screening.
Individuals selected for both the prostate cancer survey and the colon cancer study will be randomized to take one of three survey types - balance sheet, rating and ranking or conjoint analysis.
These surveys will help participants clarify their values and opinions about screening options for colon cancer or prostate cancer.
Participants' responses to the online survey are measured at one point in time - the time at which the participant takes the survey.
研究概览
地位
完全的
详细说明
This study will compare effect of a conjoint analysis based values clarification exercise, ranking and rating, and a balance sheet on screening test preferences for colorectal cancer screening and prostate cancer screening using online surveys.
Recruitment will be conducted through Survey Sampling International (SSI), an online survey research firm.
Participants will be randomized to one of three arms to take online surveys.
Patients will complete either a conjoint analysis task, in which they will be asked to make a series of choices between hypothetical screening testing strategies with different attributes; a rating and ranking task for these same attributes; or they will make a choice after viewing a balance sheet of attributes.
研究类型
介入性
注册 (实际的)
1831
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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North Carolina
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Chapel Hill、North Carolina、美国、27599
- Cecil G. Sheps Center for Health Services Research
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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
50年 至 75年 (成人、年长者)
接受健康志愿者
是的
有资格学习的性别
全部
描述
Inclusion Criteria:
Colorectal cancer
- men and women, ages 50-75, who can speak and read English.
Prostate cancer screening
- men, ages 50-75, who can speak and read English.
Exclusion Criteria:
Colorectal Cancer
- individuals with a previous personal or family history of colon cancer, personal history of polyps, or inflammatory bowel disease will be excluded.
Prostate cancer
- individuals with a previous personal or family history of prostate cancer will be excluded
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：卫生服务研究
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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其他：Rating and Ranking Group
A group of individuals from the United States and Australia who complete a rating and ranking task.
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Individuals who are randomized to the rating and raking arm will be asked to complete an informational task in a rating and ranking format.
The task will help individuals clarify their opinions and preferences regarding colon cancer and prostate cancer screening.
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其他：Discrete Choice Group
A group of individuals from the United States and Australia who complete a discrete choice experiment task.
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Individuals who are randomized to the rating and raking arm will be asked to complete an informational task in a discrete choice format.
The task will help individuals clarify their opinions and preferences regarding colon cancer and prostate cancer screening.
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其他：Balance Sheet Group
Individuals from the United States and Australia who will complete an implicit values clarification task
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Individuals who are randomized to the rating and raking arm will be asked to complete an informational task in a balance sheet format.
The task will help individuals clarify their opinions and preferences regarding colon cancer and prostate cancer screening.
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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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Participant-reported most important attribute from survey
大体时间：1 day
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The single most important colon cancer or prostate cancer screening attribute indicated by the participant surveys.
Each participant will be randomly assigned to take one of three survey versions: either (1) a conjoint analysis task wherein they will be asked to make a series of choices between hypothetical screening testing strategies with different attributes; (2) a rating and ranking task for these same attributes; or (3) they will make a choice after viewing a balance sheet of attributes.
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1 day
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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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Participant-reported intent to undergo screening from survey
大体时间：1 day
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the number of participants who state they plan to be screened for condition
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1 day
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Unlabeled screening test options
大体时间：1 day
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choice on a single question among unlabeled screening test options
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1 day
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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：Michael Pignone, MD, MPH、University of North Carolina, Chapel Hill
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
一般刊物
- Brenner A, Howard K, Lewis C, Sheridan S, Crutchfield T, Hawley S, Reuland D, Kistler C, Pignone M. Comparing 3 values clarification methods for colorectal cancer screening decision-making: a randomized trial in the US and Australia. J Gen Intern Med. 2014 Mar;29(3):507-13. doi: 10.1007/s11606-013-2701-0. Epub 2013 Nov 23.
- Howard K, Brenner AT, Lewis C, Sheridan S, Crutchfield T, Hawley S, Nielsen ME, Pignone MP. A comparison of US and Australian men's values and preferences for PSA screening. BMC Health Serv Res. 2013 Oct 5;13:388. doi: 10.1186/1472-6963-13-388.
- Pignone MP, Howard K, Brenner AT, Crutchfield TM, Hawley ST, Lewis CL, Sheridan SL. Comparing 3 techniques for eliciting patient values for decision making about prostate-specific antigen screening: a randomized controlled trial. JAMA Intern Med. 2013 Mar 11;173(5):362-8. doi: 10.1001/jamainternmed.2013.2651.
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
2011年7月1日
初级完成 (实际的)
2011年10月1日
研究完成 (实际的)
2011年10月1日
研究注册日期
首次提交
2012年2月7日
首先提交符合 QC 标准的
2012年3月19日
首次发布 (估计)
2012年3月20日
研究记录更新
最后更新发布 (实际的)
2017年4月25日
上次提交的符合 QC 标准的更新
2017年4月21日
最后验证
2012年7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.