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NCT06707155Completed

Digital Tracking With Auto Data Reporting

Study on the Use of Digital Platforms for the Control of Insulin Treatment in Patients With Type 1 Diabetes Mellitus

Source: ClinicalTrials.gov · Last updated 5 Jun 2025

Brief summary (registry, in English)

Type 1 diabetes mellitus is a chronic pathology and represents a constant challenge for children and adolescents with diabetes and their families. The objective of the treatment of DM1 in pediatric age is to achieve and maintain an optimal glycemic control in order to avoid or delay chronic micro- and macrovascular complications related to the disease. However, currently, despite technological advances and the development of new insulin formulations, the majority of patients are unable to achieve glycemic goals. In this context, the use of digital tools/platforms that allow remote monitoring of patients and that facilitate telemedicine have shown potential to improve treatment adherence and facilitate continued therapeutic education, improving clinical results with savings in time and associated costs.

Status (registry)
Completed
Study type
Observational
Enrollment
25 (actual)
First submitted
19 Nov 2024
Start date
22 Jul 2024
Primary completion date
4 Jan 2025
Lead sponsor
Persei Vivarium
NCT number
NCT06707155

What you commit to

  • Study type: Observational
  • Participants enrolled: 25
  • From 22 Jul 2024 to the primary completion date, 4 Jan 2025
  • 1 site 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.

Other

  • Patients who, in the opinion of the investigator will not be able to commit to carrying out the follow-ups or do not have adequate technological skills

Who the study is looking for

  • Patients with type 1 diabetes mellitus
  • Patients treated with subcutaneous insulin in multiple daily doses or patients treated with subcutaneous insulin in continuous subcutaneous infusion systems
  • Patients using a glucose monitoring system
  • Patients who are able to complete the study questionnaires
  • Patients who are able to handle the application on a smart mobile phone.
  • Informed consent is obtained from the patient.

Age in the registry: 3 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hospital Infantil Universitario Nino Jesus
Coordinator of this site? Confirm its status
MadridSpainUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.