Efficacy and Safety of a Medication Dose Reminder Feature in a Digital Health Offering With the Use of Sensor-Enabled Medicines
Initiatives
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This study assessed the efficacy and safety of "seeing" versus "not seeing" medication dose reminders regarding medication adherence and risk for overdose.
Note: All published information has been collected from the article referenced in the Marker Paper box below. Therefore, there may be variations with more advanced versions of the study.
- Start Year
- 2015
- End Year
- 2015
Design
- Study design
- Clinical trial cohort
Marker Paper
Moorhead P, Zavala A, Kim Y, Virdi NS. Efficacy and safety of a medication dose reminder feature in a digital health offering with the use of sensor-enabled medicines. J Am Pharm Assoc (2003). 2017;57(2):155‐161.e1. doi:10.1016/j.japh.2016.12.067
PUBMED 28159505
Recruitment
- Sources of Recruitment
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- Individuals
Number of participants
- Number of participants
- 57
- Number of participants with biosamples
Access
Availability of data and biosamples
| Data | |
| Biosamples | |
| Other |
Timeline
Adult subjects with uncontrolled hypertension and DM.
Adult subjects (18 years of age or older) with uncontrolled hypertension and DM.
Selection Criteria
- Minimum age
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18
- Newborns
- Twins
- Countries
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- United States of America
- Ethnic Origin
-
- Health Status
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- uncontrolled hypertension (systolic blood pressure 140 mmHg) taking at least 2 antihypertensives and uncontrolled diabetes mellitus type 2 (A1C 7%) on metformin or sulfonylurea.
Recruitment
Number of participants
- Number of participants
- 57
- Number of participants with biosamples
Data Collection Event
Subjects enrolled in this study were assigned to either use digital health (DH) with the use of sensor-enabled medicines (coencapsulated medicines with an ingestible sensor) for 4 or 12 weeks or receive usual care based on a cluster-randomized design. All subjects were followed for 12 weeks.
- Start Date
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2015-10
- End Date
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2015-12
- Data sources
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Smart sensors
- proteus sensor
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Smart sensors