Coronary Artery Disease Clinical Trial
Official title:
Evaluating Individual and Patient-Selected Family/Friend/or Reciprocal Peer Notifications to Improve Statin Medication Adherence Among Patients With Coronary Artery Disease
The purpose of this research study is to improve statin medication adherence among Veterans with coronary artery disease with poor adherence to medications. The investigators are testing if newer technology pill bottle devices linked with individual feedback and/or social incentive strategies can improve medication taking behavior.
Patients with coronary artery disease and previous poor adherence to statin medications will
be recruited at Philadelphia VA Medical Center. Enrolled participants will be randomly
assigned to one of three arms:
1. Control Group
2. Individual Alarm device and feedback report
3. Individual plus patient-selected Feedback Friend report
Patients will be given a medication-monitoring device (Vitality GlowCaps) to monitor the
statin medication that is being currently prescribed by their primary care physician. In
first group, the control arm (Arm 1), the device reminders will be turned off but the device
will continue recording adherence to the medications. In second group, reminder arm (Arm 2),
the device will be programmed as an alarm that will be activated if the patient does not take
the medication at the time set by the patient. In addition the patient will get a weekly
report of his/her adherence. In the third group, patient-selected family/friend/or reciprocal
peer feedback arm (Arm 3), in addition to the activation of the alarm function the device
will be linked to a weekly report on adherence to medications. This report will be delivered
to the patient and to the patient identified family/friend/ or reciprocal peer.
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