KCT0007220尚未招募未知
Evaluation of electronic PRO application system for chemotherapy-induced side effects and symptom monitoring
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 372
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 20?(Year) 至 o Limit（—）
- 性别
- All
入选标准
- •1) 20 years of age or older (if necessary due to the nature of the disease, people aged 70 or older may be included in this study with the consent of their caregivers according to the decision of the healthcare professionals)
- •2) diagnosed with breast, endometrial, colon, or lung cancer;
- •planning to receive the first cycle of therapy (for both curative and palliative intent) or one year has been passed after the end of therapy (for curative intent only)
- •3) 0 or 1 in ECOG (Eastern Cooperative Oncology) performance status
- •4) capable to use a smartphone (Android OS only) and mobile applications
- •5) understanding the purpose of this study and expressing willingness to participate in this study
排除标准
- •1) judged by the researcher to be restricted from participating in this study
- •2) planned to receive concurrent chemoradiation therapy (CCRT)
- •3) determined by the researcher to be unable to participate in this study
研究者
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