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Clinical Trials/NCT03753568
NCT03753568
Unknown
Not Applicable

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

Helsinki University Central Hospital1 site in 1 country100 target enrollmentMarch 20, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anticoagulant Drugs
Sponsor
Helsinki University Central Hospital
Enrollment
100
Locations
1
Primary Endpoint
Adherence to the medication
Last Updated
7 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
March 20, 2019
End Date
September 1, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Janne Sahlman

Chief medical officer, Popit Ltd

Helsinki University Central Hospital

Eligibility Criteria

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

Outcomes

Primary Outcomes

Adherence to the medication

Time Frame: 8 months

PDC - proportion of days covered

Secondary Outcomes

  • Variation of daily pill taking times(8 months)

Study Sites (1)

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