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Taking people in SpainNo phase

Testing a Mobile App to Guide Insulin Dosing in Diabetes

Tests a phone app for insulin dosing in adults with type 1 diabetes.

Plain-language title generated from the registry record
Registry title: Evaluation of a Mobile AI-powered Decision Support System for Insulin Dosing and Glucose Prediction in Type 1 Diabetes: The glUCModel Clinical Trial Protocol

Key facts

Where
Madrid and Toledo, SpainSee the 2 sites

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 18 to 65 with type 1 diabetes. They use multiple daily insulin injections (basal and bolus) and wear a CGM linked to their phone. The trial tests a mobile app that supports insulin dosing.

Age
18 to 65 years
Sex
All sexes can join.
Disease stage
Type 1 diabetes for at least one year, with HbA1c below 9% (75 mmol/mol).
Earlier treatment
Must currently follow multiple daily injection therapy with basal and bolus insulin.
Biomarker or test result
HbA1c below 9% (75 mmol/mol). A CGM (continuous glucose monitor) connected to a mobile phone must be worn.

Main reasons for not taking part

  • Significant psychiatric disorder
  • Treatment with corticoids
  • Hospitalization or surgery in the last six months
  • Pregnancy or planning a pregnancy
  • Cannot use a mobile app or manage insulin dosing actively

Read by machine on 12 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Source: NCT07304778, who can take part

Where in Spain

  • Universidad Complutense de MadridMadrid, SpainContact: Ignacio Hidalgo, PhDNot yet recruiting
  • Hospital Universitario de ToledoToledo, SpainContact: Esther Maqueda, MDTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Universidad Complutense de Madrid
Trial code
NCT07304778
Record updated
6 January 2026
Original description
The goal of this clinical trial is to evaluate the safety and efficacy of integrating predictive models into insulin therapy management via the user-centered glUCModel mobile app in People with Type 1 Diabetes Mellitus following Multiple Insulin Dosing therapy. Participants will be aged 18 to 65 years. The main questions it aims to answer are:Read full original descriptionShow less

Evaluation of a Mobile AI-powered Decision Support System for Insulin Dosing and Glucose Prediction in Type 1 Diabetes: The glUCModel Clinical Trial Protocol

The goal of this clinical trial is to evaluate the safety and efficacy of integrating predictive models into insulin therapy management via the user-centered glUCModel mobile app in People with Type 1 Diabetes Mellitus following Multiple Insulin Dosing therapy. Participants will be aged 18 to 65 years. The main questions it aims to answer are:

Does using the app improve glycaemic control, as measured by time in range? Does using the app reduce the number of episodes of hyperglycaemia and hypoglycaemia? Are the app's design and functionality adequate?

The study will comprise four phases:ses}):

* Screening phase: Informed consent, collection of sociodemographic and clinical data, and baseline Pittsburg, IFIS, and DTSQ questionnaires. * Run-in phase: 2 weeks of standard care with CGM. Data will be used to generate personalized predictive models in the intervention group. * Active treatment phase: Participants continue MDI therapy. The intervention group will additionally use the glUCModel mobile app. CGM data from the final 2 weeks will be analyzed. * Evaluation and analysis phase: Participants will complete the uMARS, Pittsburgh, and DTSQ questionnaires. Statistical analysis and correlations among outcomes will be processed.

Inclusion: HbA1c < 9%; Currently following an MDI Bolus-Basal therapy; Wearing CGMs connected to a mobile phone; Spanish language proficiency; Willingness to participate in the trial; At least one year since the time of diabetes diagnosis; Ability to use a mobile application like glUCModel; Own a mobile phone running Android or iOS operating system; Ability to follow a Portion-controlled diet for diabetes; Educated to do an active management of insulin dosing.

Exclusion: Subjects in treatment with corticoids; Patients who have required hospitalization or surgery in the last six months; Less than one year since the time of diabetes diagnosis; Unable to follow a Portion-controlled diet for diabetes; Diagnosed with a significant psychiatric disorder; HbA1c < 9%; Not wearing CGMs; Non-Spanish language proficiency; Unable to use a mobile application like glUCModel; Unable to do an active management of insulin dosing; Pregnancy or planning a pregnancy.

ClinicalTrials.gov NCT07304778