Perspectives Patient Education Randomized Study
- Conditions
- Medication Adherence
- Interventions
- Device: MyIDEA
- Registration Number
- NCT04439864
- Lead Sponsor
- University of Illinois at Chicago
- Brief Summary
This is a randomized clinical trial evaluating the educational program called My Interventional Drug Eluting Stent Educational App (MyIDEA) that is a pilot at two sites.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 45
- received a drug eluting stent during a Percutaneous Coronary Intervention (PCI) during a hospitalization for the PCI procedure,
- were greater than 50 years old (funding agency requirement),
- spoke and understood English.
- inability to give informed consent
- allergy to aspirin
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description MyIDEA MyIDEA Research Participants interacted with MyIDEA program both in the hospital and in the follow up cardiology appointment.
- Primary Outcome Measures
Name Time Method Feasibility of study design engaging elderly patients in novel tablet based education. 3 months Would research participants enroll and follow up in a study of tablet based education. Do patients think they know everything? Would patients enrolled in the control arm still follow up in the study?
- Secondary Outcome Measures
Name Time Method Medication adherence 3 months A measure of Pharmacy days covered for DAPT medication. The patients after recieving a Drug Eluting Stent need to adhere to Dual Antiplatlet Therapy (DAPT) to prevent restenosis of the stent. PDC is a calculation of the DAPT which is Aspirin and an ADP receptor antagonist. As aspirin is over the counter, the pharmacy does not have a record of purchase so the PDC was calculated for the ADP receptor antagonis.