My MediHealth: A Paradigm for Children-centered Medication Management (mymedihealth)
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.
|Study Design:||Observational Model: Case Control
Time Perspective: Prospective
|Official Title:||My MediHealth: A Paradigm for Children-centered Medication Management|
- Change in baseline asthma self efficacy after 3 weeks [ Time Frame: 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. ] [ Designated as safety issue: No ]Will assess self-efficacy using the survey by Bursch and colleagues (1997)
- Change in medication adherence after 3 weeks [ Time Frame: Participants will be followed for 4 weeks, with measurements at baseline and the end of 3 weeks ] [ Designated as safety issue: Yes ]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.
|Study Start Date:||May 2012|
|Primary Completion Date:||October 2012 (Final data collection date for primary outcome measure)|
Group receiving access to MyMediHealth web site.
Children completing baseline and week two measures, but without any additional intervention.
Other: MyMediHealth access
Patients who will be given access to a web-based medication scheduling and SMS-based reminder system.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01730235
|United States, Tennessee|
|Vandebilt Monroe Carell Children's Hospital|
|Nashville, Tennessee, United States, 37232|