App aims to boost ozempic adherence in diabetes patients
NCT ID NCT06478550
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a smartphone app helps people with type 2 diabetes stick with their weekly Ozempic injections. 304 participants either used the app or received standard care. The study tracked how long they stayed on the medication and if they reached their target dose.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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304 people
The number who actually took part.
- Started
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Jun 2024
- Finished
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Apr 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Participants with type 2 diabetes.
- Ages
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25 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Signed consent obtained before any study-related activities (study-related activities are any procedure related to recording of data according to the protocol). * The decision to initiate treatment with commercially available semaglutide s.c. has been made by the patient and the Health Care Providers (HCP) and independently from the decision to include the patient in this study. Patients can be randomised up to 10 days after being prescribed semaglutide. * Treatment with semaglutide s.c. is needed for intensification of glycaemic control and used according to label as judged by HCP. * Male or female; aged 25-75 years (both inclusive) at the time of signing informed consent. * Diagnosed with type 2 diabetes (T2D) at least 180 days prior to obtaining informed consent. * Willing to comply with the protocol requirements which includes use of Patient Support Solution (PSS) app on own mobile device (iphone Operating System (iOS) 11 (or higher) and Android 4.1 (or higher) devices), using Mallya®, filling out questionnaires as judged by the HCP. Exclusion Criteria: * Previous participation in this study. Participation is defined as having given informed consent in this study. * Treatment with any investigational drug within 30 days prior to enrolment into the study. * Glucagon Like Peptide-1 Receptor Agonist (GLP-1 RA) use for 90 days prior to randomisation. However, one prescription of once-weekly semaglutide subcutaneously (s.c.) is allowed up to 10 days prior to randomisation. * Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation. * Use of pacemaker or body worn infusion pumps according to Mallya®'s instruction for use. * Impaired eyesight prohibiting readability of PSS app provided on mobile device. * Inability to independently self-manage anti-diabetic treatments received as judged by HCP. * Inability to independently inject semaglutide s.c. treatment as judged by HCP. * Inability to fulfil study requirement as judged by the HCP.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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"Laiko" General Hospital of Athens
Goudi/Athens, 11527, Greece
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General Hospital Of Thessaloniki Papageorgiou
Thessaloniki, Nea Efkarpia, 56429, Greece
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General Hospital of Thessaloniki 'G. Gennimatas
Thessaloniki, 54635, Greece
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Geniko Nosokomeio Peiraia Tzaneio
Piraeus, 18536, Greece
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Univ Gen Hospital Larisa
Larissa, 41110, Greece
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University Hospital of Athens ATTIKON
Athens, Attica, 12462, Greece
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