Is a Smartphone Application Effective as an Oral Medication Adherence Aid
Status: | Terminated |
---|---|
Conditions: | High Blood Pressure (Hypertension), High Cholesterol |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 11/22/2017 |
Start Date: | October 30, 2013 |
End Date: | November 14, 2017 |
This research will act as a pilot study that will be conducted to determine the effectiveness
of a smartphone medication adherence application on adherence to oral hypertensive, diabetic,
and dyslipidemic medications using a prospective randomized design. Subjects will be
recruited from the University of Arkansas for Medical Sciences (UAMS) Internal Medicine
Clinic North, and the study data will be collected using only subject self-reports and
subject pharmacy records.
of a smartphone medication adherence application on adherence to oral hypertensive, diabetic,
and dyslipidemic medications using a prospective randomized design. Subjects will be
recruited from the University of Arkansas for Medical Sciences (UAMS) Internal Medicine
Clinic North, and the study data will be collected using only subject self-reports and
subject pharmacy records.
Inclusion Criteria:
- Males and females at least 18 years of age
- Provide informed consent
- Prescribed an oral medication indicated for hypertension, diabetes, or dyslipidemia
during 12 weeks pre-enrollment
- Own a smartphone (Android or iOS) with unlimited text messaging, email access, and app
store access
- Oral confirmation that the subject has not previously used a medication adherence app
- Able to consult with a pharmacy or medical student during the recruitment process for
purposes of consent, data collection, and/or medication reconciliation, and/or
MyMedSchedule registration
Exclusion Criteria:
- Severely impaired vision
- Reside in a nursing home
- Non-ambulatory/bedridden
- Not fluent in English
We found this trial at
3
sites
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Little Rock, Arkansas 72205
Principal Investigator: Paul H Anderson
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Little Rock, Arkansas 72211
Principal Investigator: Paul H Anderson
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