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临床试验/NCT04994691
NCT04994691已完成不适用

Effect of Varied Outreach Methods on Appointment Scheduling and Appointment Completion Using MyChart

Children's Hospital Medical Center, Cincinnati1 个研究点 分布在 1 个国家目标入组 945 人开始时间: 2021年7月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
945
试验地点
1
主要终点
Number of Participants Who Completed Well Child Check Visit

研究概览

简要总结

Our objective is to determine the effectiveness of varied outreach methods (e.g. standard versus tailored MyChart messaging) to children age 6-17 years old who are due for a WCC visit and don't have one scheduled in the next 45 days on the outcomes of appointment scheduling and appointment completion.

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
6 Years 至 17 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •age 6-17 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

  • •no active MyChart account

研究组 & 干预措施

No message

Placebo Comparator

No message sent

干预措施: No Message (Other)

Standard message

Active Comparator

2 MyChart reminders that child is overdue for well child check visit

干预措施: Standard message (Other)

Tailored message

Active Comparator

2 MyChart reminders that child is overdue for well child check visit with date of last WCC and age

干预措施: Tailored message (Other)

结局指标

主要结局

Number of Participants Who Completed Well Child Check Visit

时间窗: Within 8 weeks of the date of intervention or the date of randomization for the control group

Participants completed well child check visit as determined by presence of a well visit billing code documentation in the electronic health record.

次要结局

  • Number of Participants Who Scheduled an Appointment for a Well Child Check Visit.(Within 8 weeks of the date of intervention or the date of randomization for the control group)
  • Number of Participants Who Received Their First COVID-19 Vaccination(Within 8 weeks of the date of the intervention or the date of randomization for the control group)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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