NCT04439864CompletedNot Applicable
Perspectives Post Percutaneous Coronary Intervention Randomized Study
Conditions
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
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
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