About this trial
We will conduct a two-group randomized controlled trial to examine the eMocha DOT intervention with pediatric HT recipients.In this population, medication nonadherence remains a primary cause of late acute rejection (LAR) episodes, increased number of hospitalizations, graft failure, and patient mortality. Herein, we propose an innovative approach to promote medication adherence and improve patient and graft outcomes.
Eligibility criteria
Qualifiers
Eligible participants are 10-21 years of age
Have received a heart transplant and are followed participating pediatric heart transplant centers
English-speaking or Spanish-speaking
Own a smart-phone or have access to the mobile app through other devices
Disqualifiers
None
Trial design
Treatments tested in this trial
- DOT intervention
Treatment groups
Sponsors and collaborators
University of Florida
Lead sponsor
emocha Mobile Health, Inc.
Collaborator
National Heart, Lung, and Blood Institute (NHLBI)
Collaborator