Diabetes (Insulin-requiring, Type 1 or Type 2)glUCModel-1NCT07304778
Evaluation of a Mobile AI-powered Decision Support System for Insulin Dosing and Glucose Prediction in Type 1 Diabetes: The glUCModel Clinical Trial Protocol
A study testing glUCModel app in people with Diabetes (Insulin-requiring, Type 1 or Type 2), run by Universidad Complutense de Madrid at 2 sites in Spain.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Diabetes (Insulin-requiring, Type 1 or Type 2)
- What is being tested?
- glUCModel app
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 34 participants
- Where
- 2 sitesSpain
- Study dates
- 11 Jul 2025to 1 Jun 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 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.
Show all 10Show fewer
- 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
Who cannot join
- 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
Show all 11Show fewer
- 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
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Spain2 sites, 2 recruiting
- Not yet recruiting
Universidad Complutense de Madrid
Madrid, Madrid, 280240
Ignacio Hidalgo, PhD, +34679562712, hidalgo@dacya.ucm.es
Jose-Manuel Velasco, PhD, +34619549105, mvelascc@ucm.es
- Recruiting
Hospital Universitario de Toledo
Toledo, Toledo, 45007
Esther Maqueda, MD, +34 679562712, esthemaq@ucm.es
J. Ignacio Hidalgo, PhD, +34913947537, HIDALGO@UCM.ES
About this study
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?
Read more
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.
Read the 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.
The glUCModel mobile application was developed to address this need. Since its early versions, it integrates proprietary, patented artificial intelligence models to provide real-time insulin recommendations, short-term glucose forecasts, and predictive alerts for hypo- and hyperglycemia. With a forecast horizon of up to two hours, the system aims to reduce glycemic variability and support timely corrective actions.
This protocol describes a randomized, open-label clinical study to evaluate the efficacy and safety of the glUCModel application in patients with T1DM using MDI therapy. The primary objective is to assess improvement in short-term glycemic control, measured by the percentage of time spent in target range (70-180 mg/dL). Secondary objectives include reductions in glycemic excursions, improved treatment satisfaction, and evaluation of usability and adherence in a real-world setting.
- Being tested
- glUCModel app
- Keywords
- Diabetes, Bolus recomendation, Artificial Intelligence
- Medical subject headings
- Diabetes Mellitus
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
glUCModel appOther
The intervention consists on using glUCModel, an application designed to help people with diabetes. It features a suite of artificial intelligence tools and statistical techniques for capturing and managing key information that people with diabetes need to track, as well as for predicting glucose values to aid users in informed decision-making.
| Study group | Role | What they receive |
|---|---|---|
| Intervention | Experimental | Participants continue MDI therapy. The intervention group will additionally use the glUCModel app. CGM data from the final 2 weeks will be analyzed Receives: Other: glUCModel app |
| Control | No intervention | Participants continue MDI therapy. CGM data from the final 2 weeks will be analyzed |
What is being measured
The primary outcome is the main question the study is designed to answer.
Time in Range (TIR)
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
Measured: During the last 2 weeks of intervention
Usability and adherence
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).
Measured: Two weeks
Secondary outcomes (13)
Frequency of Level 1 hypoglycemia
Frequency in minutes of Level 1 hypoglycemia (40 ≤ CGM glucose < 55).
Measured: During the last 2 weeks of intervention
Frequency of Level 2 hypoglycemias
Frequency in minutes of Level 2 hypoglycemia (55 ≤ interstitial glucose ≤ 70)
Measured: During the last 2 weeks of intervention
Frequency of Level 1 hyperglycemias
Frequency in minutes of Level 1 hyperglycemia (180 ≤ CGM glucose ≤ 240).
Measured: During the last 2 weeks of intervention
Frequency of Level 2 hyperglycemias
Frequency in minutes of Level 2 hyperglycemia (241 ≤ interstitial glucose ≤ 400).
Measured: During the last 2 weeks of the intervention
Duration of Level 1 hypoglycemias
Average Duration in minutes of Level 1 hypoglycemia (40 ≤ CGM glucose < 55)
Measured: During the last 2 weeks of intervention
Duration of Level 2 hypoglycemia
Average duration in minutes of Level 2 hypoglycemia (55 ≤ interstitial glucose ≤ 70).
Measured: During the last 2 weeks of intervention
Duration of Level 1 hyperglycemias
Average duration in minutes of Level 1 hyperglycemia (180 ≤ CGM glucose ≤ 240).
Measured: During the last 2 weeks of intervention
Duration of Level 2 hyperglycemias
Average duration in minutes of Level 2 hyperglycemia (241 ≤ interstitial glucose ≤ 400).
Measured: During the last 2 weeks of the intervention
Glycemic coefficient of variation
Coefficient of Variation (CV) is calculated using the mean and the standard deviation of the glucose values. Coefficient of Variation (CV) is calculated by dividing the Standard Deviation by the mean of the glucose values.
Measured: During the last 2 weeks of intervention
Glycemic variability
Glycemic variability is computed as the standard deviation. Standard Deviation (SD) is measured as the dispersion of glucose values from the average.
Measured: During the last 2 weeks of intervention
Accepted Recommendations
Percentage of insulin recommendations accepted and applied by the user from the total number of recommendations requested.
Measured: During the last 2 weeks of intervention
Quality of predictions
Quality of predictions measured using the Parkes Errod Grid analysis.
Measured: During the last 2 weeks of intervention
Treatment satisfaction
Treatment satisfaction using the Diabetes Treatment Satisfaction Questionnaire (DTSQ)
Measured: last 2 weeks of the intervention
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Dec 2025
- Study start11 Jul 2025
- Primary completion1 Feb 2026 (estimated)
- Study completion1 Jun 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Diabetes (Insulin-requiring, Type 1 or Type 2)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 34 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Universidad Complutense de Madrid
- Sponsor type
- University, hospital or other
- Collaborators
- Bioinspired Intelligence SL, Hospital de Toledo
- Responsible party
- Principal investigator, J. Ignacio Hidalgo, Universidad Complutense de Madrid
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07304778
- Sponsor's protocol ID
- glUCModel-HUT
- Other IDs
- PDC2022-133429-I00, PID2021-125549OB-I00, PID2024-158129OB-I00
- Acronym
- glUCModel-1
- Status last verified
- Dec 2025
- First submitted
- 30 Nov 2025
- Last updated
- 6 Jan 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: It depends on the autorization of the University
Study at a glance
From the registry record, last updated by the sponsor on 6 Jan 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official 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
- ClinicalTrials.gov ID
- NCT07304778
- Acronym / sponsor ID
- glUCModel-1 / glUCModel-HUT
- Keywords
- Diabetes, Bolus recomendation, Artificial Intelligence
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 34 participants (estimated)
- Lead sponsor
- Universidad Complutense de MadridUniversity, hospital or other
- Collaborators
- Bioinspired Intelligence SL, Hospital de Toledo
- Study start
- 11 Jul 2025 (actual)
- Primary completion
- 1 Feb 2026 (estimated)
- Study completion
- 1 Jun 2026 (estimated)
- First posted
- 26 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
The glUCModel mobile application was developed to address this need. Since its early versions, it integrates proprietary, patented artificial intelligence models to provide real-time insulin recommendations, short-term glucose forecasts, and predictive alerts for hypo- and hyperglycemia. With a forecast horizon of up to two hours, the system aims to reduce glycemic variability and support timely corrective actions.
This protocol describes a randomized, open-label clinical study to evaluate the efficacy and safety of the glUCModel application in patients with T1DM using MDI therapy. The primary objective is to assess improvement in short-term glycemic control, measured by the percentage of time spent in target range (70-180 mg/dL). Secondary objectives include reductions in glycemic excursions, improved treatment satisfaction, and evaluation of usability and adherence in a real-world setting.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Intervention | Experimental | Other: glUCModel appParticipants continue MDI therapy. The intervention group will additionally use the glUCModel app. CGM data from the final 2 weeks will be analyzed |
| Control | No intervention | –Participants continue MDI therapy. CGM data from the final 2 weeks will be analyzed |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (10 listed)
- HbA1c < 9%
- Currently following an MDI Bolus-Basal therapy.
Key exclusion criteria (11 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| glUCModel appThe intervention consists on using glUCModel, an application designed to help people with diabetes. It features a suite of artificial intelligence tools and statistical techniques for capturing and managing key information that people with diabetes need to track, as well as for predicting glucose values to aid users in informed decision-making. | Other | Intervention |
Primary outcome
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).
13 secondary outcomes
Frequency of Level 1 hypoglycemia
Time frame: During the last 2 weeks of intervention
Frequency of Level 2 hypoglycemias
Time frame: During the last 2 weeks of intervention
Frequency of Level 1 hyperglycemias
Time frame: During the last 2 weeks of intervention
Frequency of Level 2 hyperglycemias
Time frame: During the last 2 weeks of the intervention
Duration of Level 1 hypoglycemias
Time frame: During the last 2 weeks of intervention
Duration of Level 2 hypoglycemia
Time frame: During the last 2 weeks of intervention
Duration of Level 1 hyperglycemias
Time frame: During the last 2 weeks of intervention
Duration of Level 2 hyperglycemias
Time frame: During the last 2 weeks of the intervention
Glycemic coefficient of variation
Time frame: During the last 2 weeks of intervention
Glycemic variability
Time frame: During the last 2 weeks of intervention
Accepted Recommendations
Time frame: During the last 2 weeks of intervention
Quality of predictions
Time frame: During the last 2 weeks of intervention
Treatment satisfaction
Time frame: last 2 weeks of the intervention
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Jan 2026.
- Individual participant dataSharing planned: Undecided. It depends on the autorization of the University
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing glUCModel app in people with Diabetes (Insulin-requiring, Type 1 or Type 2), run by Universidad Complutense de Madrid at 2 sites in Spain.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 10 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 6 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Ignacio Hidalgo, PhD (+34679562712, hidalgo@dacya.ucm.es), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Time in Range (TIR) (time frame: During the last 2 weeks of intervention). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Jan 2026.