NCT06478550Completed
A Research Study to Understand How People With Type 2 Diabetes Take Ozempic® and if the Ozempic®App Helps Them Stay on This Treatment
A Pilot Study Investigating the Effect of Patient Support Solution App With Connectivity on Once-weekly Semaglutide s.c. Treatment Persistence in Patients With Type 2 Diabetes in a Clinical Practice Setting
Source: ClinicalTrials.gov · Last updated 11 Feb 2026
Brief summary (registry, in English)
This study looks at how participants with type 2 diabetes take Ozempic® and if the Ozempic® app helps participants to stay on this treatment. Participants will already be prescribed with Ozempic® by the study doctor. Participants may be asked to use a device called Mallya®, which participants must attach to their Ozempic® injection pen. Participants might also be asked to install an Ozempic® app on their mobile phone which supports the participants in the use of Ozempic®. At the beginning and at the end of this study, the participants will have to fill out some questionnaires about their diabetes treatment. Participants may also be chosen to participate in a voluntary non-mandatory interview after the study has ended. The total duration of study is approximately 10 months.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 304 (actual)
- First submitted
- 24 Jun 2024
- Start date
- 26 Jun 2024
- Primary completion date
- 23 Apr 2025
- Lead sponsor
- Novo Nordisk A/S
- Diseases
- Type 2 diabetes
- NCT number
- NCT06478550
What you commit to
- Study type: Observational
- Participants enrolled: 304
- From 26 Jun 2024 to the primary completion date, 23 Apr 2025
- 6 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- 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.
- Inability to independently self-manage anti-diabetic treatments received as judged by HCP.
Other
- 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 inject semaglutide s.c. treatment as judged by HCP.
- Inability to fulfil study requirement as judged by the HCP.
Who the study is looking for
- 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.
Age in the registry: 25 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (6)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University Hospital of Athens ATTIKON Coordinator of this site? Confirm its status | Athens | Greece | Unknown status |
| "Laiko" General Hospital of Athens Coordinator of this site? Confirm its status | Goudi/Athens | Greece | Unknown status |
| Univ Gen Hospital Larisa Coordinator of this site? Confirm its status | Larissa | Greece | Unknown status |
| Geniko Nosokomeio Peiraia Tzaneio Coordinator of this site? Confirm its status | Piraeus | Greece | Unknown status |
| General Hospital of Thessaloniki Papageorgiou Coordinator of this site? Confirm its status | Thessaloniki | Greece | Unknown status |
| General Hospital of Thessaloniki G. Gennimatas Coordinator of this site? Confirm its status | Thessaloniki | Greece | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.