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Clinical Trials/NCT07304778
NCT07304778RecruitingNot Applicable

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

Universidad Complutense de Madrid2 sites in 1 country34 target enrollmentStarted: July 11, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
34
Locations
2
Primary Endpoint
Time in Range (TIR)

Study Overview

Brief Summary

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.

Detailed Description

Diabetes mellitus is a chronic, metabolic disorder characterized by impaired regulation of blood glucose, affecting more than 400 million people worldwide. Insulin, a hormone produced by the pancreas, facilitates the uptake of glucose into cells for energy production. In diabetes, either insufficient insulin is produced or the body cannot use it effectively, leading to persistent hyperglycemia. Over time, uncontrolled glucose levels can result in serious complications, including cardiovascular disease, neuropathy, retinopathy, and nephropathy. Effective management is therefore essential to prevent both acute and long-term adverse outcomes.

Two main forms of diabetes can be distinguished. Type 1 diabetes mellitus (T1DM) is an autoimmune condition in which pancreatic β-cells are destroyed, resulting in absolute insulin deficiency. It accounts for approximately 10% of all cases. Individuals with T1DM require lifelong insulin replacement therapy, typically delivered as multiple daily injections (MDI) or via an insulin pump. In contrast, type 2 diabetes mellitus (T2DM), the more prevalent form, is characterized primarily by insulin resistance. While insulin production is preserved in early stages, progressive dysfunction may ultimately necessitate pharmacological therapy, including insulin. Lifestyle interventions such as healthy diet and physical activity can delay or prevent T2DM onset and progression.

For individuals with diabetes, day-to-day self-management requires frequent glucose monitoring and insulin dose adjustments that must take into account meals, physical activity, stress, illness, and other factors. Capillary glucose meters and, more recently, continuous glucose monitoring systems (CGMs) have greatly improved access to real-time glucose data. However, interpreting these data and deciding on corrective actions remains challenging, and errors in insulin dosing can lead to hypoglycemia or persistent hyperglycemia. Both acute complications and the constant decision-making load contribute to reduced quality of life and treatment fatigue.

To support patients in these complex tasks, predictive models of glucose dynamics have been extensively investigated. Accurate prediction could enable early warnings of hypo- or hyperglycemia and assist in optimizing insulin therapy. The ultimate vision is the development of a fully automated ''artificial pancreas'' combining glucose sensing, insulin delivery, and robust prediction algorithms. Various machine learning (ML) approaches have been explored for glucose forecasting, including Genetic Programming , K-Nearest Neighbours , Grammatical Evolution, and, most prominently, Neural Networks. Among neural architectures, Long Short-Term Memory (LSTM) and other recurrent models have demonstrated strong performance for time-series data such as CGM traces, although convolutional and multilayer perceptron (MLP) networks have also been applied. Despite encouraging results, challenges remain in ensuring accuracy, robustness, and real-world usability across diverse patient populations.

Managing T1DM, particularly in patients using MDI, continues to pose a major challenge. While CGM and insulin pumps have improved outcomes, decisions about insulin dosing still depend heavily on patient intuition and experience, leaving room for error and variability. There is therefore a clear need for decision-support tools that combine predictive analytics with personalized recommendations to enhance safety, autonomy, and treatment adherence.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • 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 Criteria

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

Outcomes

Primary Outcomes

Time in Range (TIR)

Time Frame: During the last 2 weeks of intervention

Time in Range (TIR), defined as the percentage of time that interstitial glucose is between 70-180 mg/dL during the final 2 weeks of the intervention phase

Time in Range (TIR)

Time Frame: During the last 2 weeks of intervention

Time in Range (TIR), defined as the percentage of time that interstitial glucose is between 70-180 mg/dL during the final 2 weeks of the intervention phase

Usability and adherence

Time Frame: Two weeks

Patient-reported outcomes on usability and adherence through uMARS. The usability of the app will be evaluated using the Spanish Version of the User Version of the Mobile Application Rating Scale (uMARS). This scale provides a comprehensive and objective measure of app usability and consists of 20 items. Each item is rated on a 5-point scale, ranging from 1 (inadequate) to 5 (excellent).

Secondary Outcomes

  • Duration of Level 2 hyperglycemias(During the last 2 weeks of the intervention)
  • Glycemic coefficient of variation(During the last 2 weeks of intervention)
  • Accepted Recommendations(During the last 2 weeks of intervention)
  • Glycemic variability(During the last 2 weeks of intervention)
  • Treatment satisfaction(last 2 weeks of the intervention)
  • Quality of predictions(During the last 2 weeks of intervention)
  • Frequency of Level 2 hypoglycemias(During the last 2 weeks of intervention)
  • Frequency of Level 2 hyperglycemias(During the last 2 weeks of the intervention)
  • Frequency of Level 1 hyperglycemias(During the last 2 weeks of intervention)
  • Frequency of Level 1 hypoglycemia(During the last 2 weeks of intervention)
  • Duration of Level 1 hypoglycemias(During the last 2 weeks of intervention)
  • Duration of Level 2 hypoglycemia(During the last 2 weeks of intervention)
  • Duration of Level 1 hyperglycemias(During the last 2 weeks of intervention)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

J. Ignacio Hidalgo

Full Professor

Universidad Complutense de Madrid

Study Sites (2)

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