Leveraging Community Engagement and Electronic Health Record Strategies to Promote Diverse Participation in Clinical Research
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 726,199
- 试验地点
- 2
- 主要终点
- Number of patients who create a research profile
研究概览
简要总结
The purpose of this study is to determine the effectiveness of enhanced features in an online patient portal including banners, a chatbot, and direct to patient message and traditional mailed letters on increasing interest in research among online patient portal users.
详细描述
The primary objective is to examine the effectiveness of enhanced online patient portal features including banners, a chatbot, and direct to patient message and traditional mailed letters on increasing interest in research among online patient portal users, as measured by the user's creation of a research profile.
The secondary objective is to examine the effectiveness of two enhanced online patient portal features including banners, a chatbot and direct-to-patient messages and traditional mailed letters on increasing participation in research among online patient portal users, as measured by the user joining a research study.
This study tests the hypothesis that at one year follow-up, various user engagement tools (e.g. messaging, banners) will increase the proportion of research profiles created by online patient portal users over profiles created by online patient portal users in the absence of those interventions.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Factorial
- 主要目的
- Other
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Has an account with the online patient portal
- •Has logged into the online patient portal at least once in the past year
- •Has not set up a research profile
排除标准
- •Currently enrolled in a clinical trial
- •Opted out of research
- •Has received a direct to patient recruitment message within the past year
- •On active cancer treatment
- •Active member of the study team
结局指标
主要结局
Number of patients who create a research profile
时间窗: 12 months
The outcome will be assessed by querying the patient's electronic medical record to determine whether the patient has registered in the Yale University Volunteer Database. This database is comprised of patients who agree to be contacted if there is a study at Yale that meets their interests.
次要结局
- Number of patients who enroll in a research study(12 months)