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My MediHealth: A Paradigm for Children-centered Medication Management (mymedihealth)

2012年11月14日 更新者:Kevin Johnson、Vanderbilt University
The last mile of the medication use system requires tools to help patients comply with medication administration rules and monitor for side effects. Personal health records (PHR) and emerging user-adopted communication tools promise to change the landscape of medication management. The overarching goal of the MyMediHealth project is to investigate ways in which PHRs and supported applications can improve the safety and quality of medication delivery. Preliminary work in this area by a team of parents, patients and school/clinic health providers created a vision for MyMediHealth, a next-generation medication management system. MyMediHealth was envisioned to allow home-based, school-based, and other caregivers to ensure safe and effective medication delivery. This vision featured just-in-time medication reminders to children with special health care needs, two-way communication to log when doses have been administered or when side effects have occurred, and mechanisms to warn caregivers about side effects and drug interactions. However, much of this work was done using prototypes, storyboards, and vision videos. Recognizing that this vision cannot be carried out without significant changes in processes and policies, the purpose of this proposed study is to evaluate the impact of medication management tools such as MyMediHealth on medication adherence for children with chronic illnesses. Specifically, the investigators hypothesize that compared with usual practice, children using mymedihealth will have improved medication adherence and will report improved (decreased) asthma symptoms.

研究概览

地位

完全的

条件

研究类型

观察性的

注册 (实际的)

115

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Tennessee
      • Nashville、Tennessee、美国、37232
        • Vandebilt Monroe Carell Children's Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

12年 至 17年 (孩子)

接受健康志愿者

是的

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Children and adolescents between the ages of 12 and 17 with a diagnosis of asthma and on at least one daily medication.

描述

Inclusion Criteria:

  • Access to the internet Caregiver agrees to let child use the Internet for the project Internet service working properly Legal guardian approves of study Child with her or his own cell phone

Exclusion Criteria:

  • non English or spanish speaking family

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
Case Group
Group receiving access to MyMediHealth web site.
Control Group
Children completing baseline and week two measures, but without any additional intervention.
Patients who will be given access to a web-based medication scheduling and SMS-based reminder system.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in baseline asthma self efficacy after 3 weeks
大体时间:participants will be followed for an average of 4 weeks, with this measure collect at the beginning of the period and after 3 weeks of reminders.
Will assess self-efficacy using the survey by Bursch and colleagues (1997)
participants will be followed for an average of 4 weeks, with this measure collect at the beginning of the period and after 3 weeks of reminders.

次要结果测量

结果测量
措施说明
大体时间
Change in medication adherence after 3 weeks
大体时间:Participants will be followed for 4 weeks, with measurements at baseline and the end of 3 weeks
At the end of the 2-week data collection period (following the 1-week test period), all participants (Control and Intervention) and their parents will be asked to complete a brief online survey, including the Asthma Control Test (ACT) and the weekly adherence survey(SDSCA). All responses collected from participants and their parents in the Time 2 Survey will be compared to those collected from the Baseline Survey, where applicable. Medication adherence will be measured by responses to ACT and SDSCA survey items for all participants.
Participants will be followed for 4 weeks, with measurements at baseline and the end of 3 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2012年5月1日

初级完成 (实际的)

2012年10月1日

研究注册日期

首次提交

2012年11月8日

首先提交符合 QC 标准的

2012年11月14日

首次发布 (估计)

2012年11月21日

研究记录更新

最后更新发布 (估计)

2012年11月21日

上次提交的符合 QC 标准的更新

2012年11月14日

最后验证

2012年11月1日

更多信息

与本研究相关的术语

其他研究编号

  • R18HS018168 (美国 AHRQ 拨款/合同)

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

MyMediHealth access的临床试验

3
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