Perspectives Post Percutaneous Coronary Intervention Randomized Study
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 45
- Primary Endpoint
- Feasibility of study design engaging elderly patients in novel tablet based education.
Study Overview
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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Other
- Masking
- Triple (Care Provider, Investigator, Outcomes Assessor)
Eligibility Criteria
- Ages
- 50 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •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.
Exclusion Criteria
- •inability to give informed consent
- •allergy to aspirin
Arms & Interventions
MyIDEA
Research Participants interacted with MyIDEA program both in the hospital and in the follow up cardiology appointment.
Intervention: MyIDEA (Device)
Treatment as normal
The research participants were given the chance to play games on the tablet and received normal clinical education.
Outcomes
Primary Outcomes
Feasibility of study design engaging elderly patients in novel tablet based education.
Time Frame: 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 Outcomes
- Medication adherence(3 months)
Investigators
Andrew D Boyd
Association Professor
University of Illinois at Chicago