MOM

Pilot Study of Digital Health Intervention via Mobile Application for Improvement of Patient Compliance and Secondary Cardiovascular Outcomes in Patients Post Percutaneous Coronary Intervention - Kwan Lee, MD

Inclusion Criteria:

1.

Subject is willing and able to give written informed consent.

2.

Subject is age > 18

3.

  1. Subject is up to 7 days post percutaneous coronary intervention with at least one drug eluting stent

OR

  1. The subject requires a staged intervention, they may be enrolled within 7 days of the staged intervention, if a PCI with a drug eluting stent is performed

4.

Subject has a personal Apple or Android smartphone with a data plan capable of supporting the mobile application of My Own Med, Inc.

5.

Subject can demonstrate the ability to use the mobile application.

6.

Subject has a designated participating caregiver who is willing and able to give written informed consent.

Exclusion Criteria:

1.

Subject has had a percutaneous coronary intervention performed greater than 7 days prior to consent.

2.

Subject has the inability to demonstrate proficiency using the mobile application My Own Med, Inc.

3.

The caregiver is unwilling to participate.

4.

Subject does not have a personally Apple or Android smartphone with a data plan capable of supporting the My Own Med, Inc. mobile application.

5.

Subject has a history of noncompliant behavior.

6.

Subject has a history of dementia or documented memory loss within the last 5 years.

For more information, contact coordinators: Ashley Larsen, golmana@shc.arizona.edu and Alyssa Crone, acrone@shc.arizona.edu