SCREEN Yourself for Cancer
SCREEN Yourself for Cancer (Self-Collection Research Examining Engagement and Navigation)
This randomized controlled trial will evaluate whether evidence-based self-sampling tools improve the cancer screening process among underscreened patients. Participants who are eligible but out-of-date for colorectal cancer screening, cervical cancer screening, or both will be randomized to either usual practice or an intervention that includes mailed self-sampling tools for the appropriate cancer screening test. Primary outcomes include screening initiation (within 12 months of enrollment) and screening completion (within 18 months of enrollment), for each cancer type. Secondary outcomes include repeat screening adherence and receipt of diagnostic resolution following abnormal screening results.
研究概览
详细说明
In the US, tens of thousands of people die from screen-preventable cancers each year. Failures occur across the entire cancer screening process, from screening initiation, to screening completion (i.e., receipt of a normal screening result or diagnostic resolution after an abnormal result), to repeat screening. Providing patients with self-sampling tools can improve these outcomes. These self-sampling tools (fecal immunochemical test [FIT] for colorectal cancer [CRC] screening and self-collected human papillomavirus [HPV] test for cervical cancer screening) enable patients to collect a sample at home and send it to a lab for testing. These tests are highly accurate and acceptable but not well-integrated into clinical care. Further, their impacts on screening completion and repeat screening are not well-studied. The proposed study is a rigorous, two-arm, parallel-groups randomized controlled trial to assess screening initiation, screening completion, and repeat screening among patients who are eligible but out-of-date with screening for CRC and/or cervical cancer. The study team will generate a census of patients in our healthcare system who meet study inclusion criteria and undertake stratified random selection to select patients for inclusion in the study. Patients will be randomized (1:1) to study arm: Usual practice arm, in which patients receive a letter informing them that they are out-of-date with cancer screening and encouraging them to make an appointment to get screened, and Self-sampling arm, in which patients receive self-sampling tool(s) and are encouraged to use it for cancer screening. As appropriate, patients will receive screening reminders, diagnostic resolution follow-up procedures, and 1-year repeat FIT for CRC screening. The study team will collect data from electronic health records and surveys. The study Aims are as follows:
Aim 1: Investigate between-arms differences in screening initiation. Aim 2: Examine between-arms differences in downstream screening outcomes. Aim 3: Identify mediators and moderators that impact the cancer screening process.
The recruitment goal for this study is 852 patients, including 542 who are eligible but out-of-date for CRC screening; 110 who are eligible but out-of-date for cervical cancer screening; and 200 who are eligible but out-of-date for both screenings. This sample will support rigorous, well-powered analyses of our Aims and hypotheses, using bivariate and multivariable analyses (including mediation and moderation analysis). This study will demonstrate the impact of self-sampling tools for the entire cancer screening process, which has significant implications for clinical care, public health, and behavioral research. The findings from the proposed study will support our long-term goal of identifying strategies to increase participation in the cancer screening process and to reduce screen-preventable cancer mortality in the US.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Leonard A. Kishel, MA
- 电话号码:321657 717-531-0003
- 邮箱:lkishel@pennstatehealth.psu.edu
研究联系人备份
- 姓名:Jennifer L. Moss, PhD
- 电话号码:323429 717-531-0003
- 邮箱:jmoss1@pennstatehealth.psu.edu
学习地点
-
-
Pennsylvania
-
Hershey、Pennsylvania、美国、17033
- Pennsylvania State University College of Medicine
-
接触:
- Leonard A Kishel, MA
- 电话号码:321657 7175310003
- 邮箱:lkishel@pennstatehealth.psu.edu
-
接触:
- Jennifer L Moss, PhD
- 电话号码:323429 7175310003
- 邮箱:jmoss1@pennstatehealth.psu.edu
-
-
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
描述
Inclusion Criteria:
- active patient at Penn State Health Department of Family and Community Medicine
- patients eligible but out-of-date for routine colorectal cancer screening and/or routine cervical cancer screening
- able to read and write in English, Spanish, or Nepali
Exclusion Criteria:
- patients ineligible for routine colorectal and/or cervical cancer screening
- patients up-to-date on routine colorectal and/or cervical cancer screening (as applicable)
- not able to read and write in English, Spanish, or Nepali
学习计划
研究是如何设计的?
设计细节
- 主要用途:放映
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器:Usual Practice
Participants will receive standard health system outreach (i.e., mailed reminders) encouraging completion of recommended colorectal and/or cervical cancer screening through routine clinical care pathways. |
Routine mailed reminders and health system communication encouraging completion of guideline-recommended cancer screening. |
|
实验性的:Self-sampling arm
Participants will receive a package containing self-sampling tool(s) for colorectal and/or cervical cancer screening, encouraging them to complete screening with the self-sampling tool. |
Education materials, instructions, and support documents accompanying mailed self-sampling kits. |
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 |
|---|---|---|
|
Colorectal cancer screening initiation
大体时间:12 months after baseline
|
The percentage of patients in each study arm who initiate colorectal cancer screening between baseline and 12-months follow-up, according to electronic health record data. |
12 months after baseline
|
|
Cervical cancer screening initiation
大体时间:12 months after baseline
|
The percentage of patients in each study arm who initiate cervical cancer screening between baseline and 12-months follow-up, according to electronic health record data. |
12 months after baseline
|
|
Colorectal cancer screening completion
大体时间:18 months after baseline
|
The percentage of patients in each study arm who complete colorectal cancer screening (i.e., receipt of a normal screening result or diagnostic resolution after an abnormal result) between baseline and 18-months follow-up, according to electronic health record data. |
18 months after baseline
|
|
Cervical cancer screening completion
大体时间:18 months after baseline
|
The percentage of patients in each study arm who complete cervical cancer screening (i.e., the receipt of a normal screening result or diagnostic resolution after an abnormal result) between baseline and 18-months follow-up, according to electronic health record data. |
18 months after baseline
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Repeat colorectal cancer screening
大体时间:24 months after baseline
|
Among patients who undergo colorectal cancer screening with FIT and receive normal test results, the percentage of patients who repeat colorectal cancer screening with FIT one year later, within 24 months of baseline, according to electronic health record data. |
24 months after baseline
|
|
Receipt of diagnostic resolution after abnormal cancer screening results
大体时间:6 months after initiating cancer screening
|
Among patients who undertake cancer screening and receive abnormal test results, the percentage of patients who receive diagnostic resolution procedures within 6 months of the test results, according to electronic health record data. |
6 months after initiating cancer screening
|
合作者和调查者
调查人员
- 首席研究员:Jennifer L. Moss, PhD、Pennsylvania State University College of Medicine
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- STUDY00029563
- 1R37CA309199-01A1 (美国 NIH 拨款/合同)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
The study team will make scientific data and associated documentation publicly available through an institutional repository upon study completion. Deidentified participant-level data supporting published findings may be shared upon reasonable request, subject to institutional approvals and applicable data use agreements.
IPD 共享时间框架
Beginning six months after final data collection, with no end date.
IPD 共享访问标准
Deidentified data and supporting information will be available to anyone through a publicly accessible, online data repository.
IPD 共享支持信息类型
- 研究方案
- 树液
- 国际碳纤维联合会
- 分析代码
- 企业社会责任
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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