Skip to content

Effect of an Electronic Reminder System on Direct Oral Anticoagulant and Oral Diabetes Medication Adherence

Effect of an Electronic Reminder System on Direct Oral Anticoagulant and Oral Diabetes Medication Adherence

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03753568
Enrollment
100
Registered
2018-11-27
Start date
2019-03-20
Completion date
2019-09-01
Last updated
2019-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anticoagulant Drugs, Diabetes Mellitus, Type 2

Keywords

medicine reminder, diabetes mellitus, type 2, direct oral anticoagulants

Brief summary

In this study, the effect of an electronic device attached to a push through pill package and a smart phone application on chronic disease medication adherence is studied.

Detailed description

In this study study two different groups of medicine users are recruited. Both groups have 50 patients each. In the first study the participants are using oral medication for diabetes and in the second study the participants use new direct oral anticoagulants. Participants use medicine reminder system consisting of an electronic device and an smart phone application. In the beginning of the study the reminder system is collecting data on how the patients are taking their medication for the first two months. Smart phone application is not providing any reminders and participants can't access the app to see the details. After two months the application will be unlocked so that it starts reminding the users to take their medication at the right time. in this phase the patients can view their medication data from the application. The reminder phase of the study lasts for two months. After these two plus two months, the results are analyzed and published. The study continues after these four months for the next four months and after that, the long term results are analyzed.' The primary outcome is the possible change in the adherence between control and active period.

Interventions

DEVICEElectronic medicine reminder system

Electronic surveillance device is attached to the participants push through pill sheet and the smart phone application reminds the participants to take their medicine if they are about to take their daily dosage.

Sponsors

Helsinki University Central Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Subjects are monitored first before the intervention and then during the intervention.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* use of direct oral anticoagulants or oral diabetic drugs * age of 18 or more * subjects have been using a smart phone

Exclusion criteria

* patients who don't use their medication without help

Design outcomes

Primary

MeasureTime frameDescription
Adherence to the medication8 monthsPDC - proportion of days covered

Secondary

MeasureTime frameDescription
Variation of daily pill taking times8 monthsThe mean difference from the mean pill taking time

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026