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临床试验/NCT01715389
NCT01715389已完成不适用

Evaluation of a Shared Decision Making Portal for Pediatric Asthma

Children's Hospital of Philadelphia2 个研究点 分布在 1 个国家目标入组 81 人开始时间: 2012年11月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
81
试验地点
2
主要终点
Acceptability of the intervention to parents and clinicians

研究概览

简要总结

This pilot intervention study will test the feasibility and acceptability and explore the outcomes of a primary care-based shared decision making (SDM) electronic medical record (EMR)-based portal that provides education, elicits and tracks patients/families' treatment concerns and goals, assesses symptoms and asthma control over time, and provides decision support to clinicians and families.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
6 Years 至 12 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Parents/legal guardians of children aged 6-12 with persistent asthma, currently receiving chronic maintenance therapy, cared for at a study practice, with consistent access to a computer with an internet connection where they feel comfortable accessing MyChart (patient portal)
  • Clinician at study site

排除标准

  • parents non-english speaking
  • child's primary care provider at the time of enrollment is a pediatric resident
  • not meeting inclusion criteria

结局指标

主要结局

Acceptability of the intervention to parents and clinicians

时间窗: 24 months

Parents and clinicians will be asked a series of open-ended questions regarding themes including satisfaction, acceptability and unintended consequences of using the portal for intervention subjects and using MyChart in general for control subjects. Subjects will also be asked a series of Likert-scaled questions related to satisfaction.

次要结局

  • Feasibility of Portal Use(24 months)
  • Shared decision making(Baseline)
  • Goal Attainment(0 months, 3 months, 6 months then Monthly)
  • Parent Activation(0 months, 3 months, 6 months)
  • Asthma-Related Quality of Life(0 months, 6 months)
  • Asthma Control(0 months, 6 months)
  • Asthma-related Utilization(3 months, 6 months)
  • Asthma Medication Adherence/Receipt(6 months)
  • Feasibility of Recruitment(24 months)
  • Feasibility of Follow-up(24 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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