Effect of Varied Outreach Methods on Appointment Scheduling, Appointment Completion, and Receipt of COVID-19 Vaccination
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 1,235
- 试验地点
- 1
- 主要终点
- Number of Participants Who Completed an Adolescent Well-care Visit
研究概览
简要总结
Our objective is to determine the effectiveness of varied outreach methods to children age 12-17 years old who are due for a well child check visit and don't have one scheduled in the next 45 days on the outcomes of appointment scheduling, appointment completion, and receipt of the COVID-19 vaccination.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- Triple (Participant, Care Provider, Outcomes Assessor)
入排标准
- 年龄范围
- 12 Years 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •age 12-17 years
- •has not had a well child check in past 365 days
- •no future well child check visit scheduled
- •parent preferred language = English or Spanish
排除标准
- •phone number not available in electronic health record
研究组 & 干预措施
No message
No message sent
干预措施: No message (Other)
Low tailored message
2 text or phone reminders that child is overdue for well child check visit
干预措施: Low tailored message (Other)
Low tailored message plus COVID-19 vaccine message
2 text or phone reminders that child is overdue for well child check visit AND COVID-19 vaccine is available
干预措施: Low tailored message plus COVID-19 vaccine message (Other)
结局指标
主要结局
Number of Participants Who Completed an Adolescent Well-care Visit
时间窗: Within 8 weeks of the date of intervention or the date of randomization for the control group
Participant completed adolescent well-care visit as determined by the presence of well-visit billing code documented in the electronic health record
次要结局
- Family Member Receipt of COVID-19 Vaccine(Within 8 weeks of the date of intervention or the date of randomization for the control group)
- Number of Participants Who Scheduled an Adolescent Well-care Appointment(Within 2 weeks of the date of intervention or the date of randomization for the control group)
- Participant Receipt of COVID-19 Vaccine(Within 8 weeks of the date of intervention or the date of randomization for the control group)