Analyzing Factors of Patient Involvement in Ovarian Cancer Clinical Trials
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 500
- 主要终点
- Patient remains in clinical trial to completion
研究概览
简要总结
Historically, participation in clinical trials has been highly skewed towards specific demographic groups. However, research identifying which trial attributes impact participation, in either positive or negative ways, is limited. This study invites participants to record a wide range of data on their clinical trial experience, with the goal being to identify factors which persistently limit patients' ability to participate in, or complete, a trial in which they were initially interested. Data will be analyzed through a range of demographic lenses, in hopes of discovering patterns which might improve the experience of future ovarian cancer patients.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Crossover
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Aged ≥ 18 years old and ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
- •Patient has been diagnosed with ovarian cancer
- •Subjects willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examination.
排除标准
- •Inability to perform regular electronic reporting
- •Patient does not understand, sign, and return consent form
- •Pregnant, breastfeeding or expecting to conceive within the projected duration of the study
结局指标
主要结局
Patient remains in clinical trial to completion
时间窗: 12 months
Patient decides to enroll in clinical trial
时间窗: 3 Months
次要结局
未报告次要终点