Evaluation of a Mobile Digital Solution for Cancer Care and Research
Evaluation of a Mobile Digital Solution for Cancer Care and Research: A Feasibility Study
研究概览
详细说明
Demographic information and patient-reported symptoms will be collected from study participants through a mobile health application called CancerLife that they can download (FREE) from their mobile device app store (Android or iOS). Participants will be asked to broadcast their emotional and physical status through a list of symptom list within the app as well as how that symptom is impacting their quality of life and activities of daily living. This data will be collected inside the application and display in easy to understand pie charts. Participants will also have the option to broadcast their entry to their social network.
Since the objective of the current feasibility study is to evaluate the feasibility and acceptability of a Mobile Digital Solution in monitoring and collecting symptom burden and QOL data, the investigators will include a standard validated instrument (FACT-G: Functional Assessment of Cancer Therapy - General) as part of this study. Participants will be asked to complete the FACT-G after initial registration and weekly for up to 4 weeks. Participants will receive electronic mail messages with a link to CancerLife weekly as a reminder to access the website.
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
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California
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Santa Monica、California、美国、90404
- John Wayne Cancer Institute at Providence Saint John's Health Center
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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
描述
Inclusion Criteria:
- Established diagnosis of cancer
- Karnofsky Index ≥50%
- Age > 18 years
Exclusion Criteria:
- Relevant cognitive impairment
- Insufficient knowledge of English language to complete the survey
学习计划
研究是如何设计的?
设计细节
- 主要用途:卫生服务研究
- 分配:不适用
- 介入模型:单组作业
- 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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实验性的:CancerLife Feasibility Group
Participants will be recruited through advertisements targeted to a specific audience using the keywords cancer and cancer survivors
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CancerLife is a mobile digital solution that allows patients to broadcast their health status inside a private invitation only group, text, email or publicly in Facebook or Instagram.
By doing, so the patient collects his/her own patient-reported outcomes data and then share this data with their doctor or care team.
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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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Feasibility/ Participation Rate
大体时间:4 weeks
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number of individuals who participate in the study divided by the number of individuals who opened the link
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4 weeks
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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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Open Rate
大体时间:4 weeks
|
number of individuals who open the link divided by total number of individuals reached by the advertisement
|
4 weeks
|
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Refusal rate
大体时间:4 weeks
|
number of individuals who declined to participate divided by the number of individuals who opened the link
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4 weeks
|
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Retention rate
大体时间:4 weeks
|
number of mission data divided by total number of items available
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4 weeks
|
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Rate of missing data
大体时间:4 weeks
|
number of mission data divided by total number of items available
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4 weeks
|
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Participant Satisfaction
大体时间:4 weeks
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describe the usability, satisfaction, and desirability of the Mobile Digital Solution using a patient experience survey at the end of the study
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4 weeks
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合作者和调查者
合作者
调查人员
- 学习椅:Santosh Kesari, MD, PhD、Saint John's Cancer Institute
研究记录日期
研究主要日期
学习开始 (实际的)
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 (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
- JWCI-17-0301
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
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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