NCT04571398Unknown不适用
A Study of ApricityRx™ Digital Therapeutic for Management of Immune-Related Adverse Events in Patients on Immuno-Oncology Therapy
适应症
试验速览
- 阶段
- 不适用
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Evaluate digital therapeutic mobile app to capture and transmit to care team patient-generated health data and access education content on IO and irAEs
研究概览
简要总结
Study of ApricityRx™ for Management of IR-AEs for patients on I-O therapy. Patients currently receiving immunotherapy will be asked to consent to participate in ApricityRx software platform mobile telephone application to report symptoms, view educational content in video form about IO and irAEs and communicate with site study team.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Confirmed cancer diagnosis
- •Prescribed treatment with immune-checkpoint inhibitor
- •Age ≥ 18 years
- •Ability to understand and the willingness to sign a written informed consent document.
排除标准
- •Uncomfortable with or unwilling to use digital or mobile technology
- •Lack of a smart phone with compatible operating systems: iOS version 10 and above, or Android 6.0 Marshmallow
- •Presence of any medical, psychological or social condition that, in the opinion of the investigator, would preclude participation in this study.
结局指标
主要结局
Evaluate digital therapeutic mobile app to capture and transmit to care team patient-generated health data and access education content on IO and irAEs
时间窗: 12 weeks
Number of times and percentage of study participants who use the app to report patient reported health data during a 12 week period and access education videos.
次要结局
未报告次要终点
研究者
研究点 (1)
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