Is a Smartphone Application Effective as an Oral Medication Adherence Aid
- Conditions
- DiabetesDyslipidemiaHypertension
- Interventions
- Other: Medication Adherence Smartphone App
- Registration Number
- NCT01968876
- Lead Sponsor
- University of Arkansas
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 68
- 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
- Severely impaired vision
- Reside in a nursing home
- Non-ambulatory/bedridden
- Not fluent in English
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Medication Adherence Smartphone App Medication Adherence Smartphone App The experimental group will receive the medication adherence app on their smartphone and will have their entire outpatient medication list pushed to the application. Text message reminders will be sent to their phones at the appropriate times.
- Primary Outcome Measures
Name Time Method Change from baseline in number of pills taken over number of pills prescribed at 4 weeks Change from baseline to 4 weeks Change from baseline in number of pills taken over number of pills prescribed at 12 weeks Change from baseline to 12 weeks
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (3)
Remedy Drug
🇺🇸Little Rock, Arkansas, United States
Internal Medicine Clinic West; University of Arkansas for Medical Sciences
🇺🇸Little Rock, Arkansas, United States
Internal Medicine Clinic North; University of Arkansas for Medical Sciences
🇺🇸Little Rock, Arkansas, United States