RECRUITINGOBSERVATIONAL
Characterization of Type 1 Diabetes Subgroup: An Artificial Intelligence Analysis of Clinical and Glucometric Features
Caracterización de Subgrupos de Personas Con Diabetes Tipo 1: análisis de características clínicas y glucométricas Utilizando Una aproximación de Inteligencia Artificial
About This Trial
The goal of this observational study is to characterize different subgroups among patients with type 1 diabetes. The main research question is: Are there distinct subtypes among people with type 1 diabetes? Participants will be invited to take part in the study by allowing access to their health data. They will not be required to undergo any additional examinations, tests, visits, or interventions.
Who May Be Eligible (Plain English)
Who May Qualify:
- Individuals with type 1 diabetes (T1D) aged 18 years or older.
- T1D individuals expected to have regular follow-up at the Endocrinology and Nutrition Department of Hospital de la Santa Creu i Sant Pau.
- Users of continuous glucose monitoring (CGM) systems for at least the last 6 months of 2024.
- Willingness and ability to provide written willing to sign a consent form to participate in the study (by the patient or his/her representative).
Who Should NOT Join This Trial:
- Presence of severe comorbidities or medical conditions that, in the investigator's judgment, could interfere with participation in the study or the interpretation of results. This circumstance is expected to be exceptional, as the study aims to be as inclusive as possible.
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
* Individuals with type 1 diabetes (T1D) aged 18 years or older.
* T1D individuals expected to have regular follow-up at the Endocrinology and Nutrition Department of Hospital de la Santa Creu i Sant Pau.
* Users of continuous glucose monitoring (CGM) systems for at least the last 6 months of 2024.
* Willingness and ability to provide written informed consent to participate in the study (by the patient or his/her representative).
Exclusion Criteria:
* Presence of severe comorbidities or medical conditions that, in the investigator's judgment, could interfere with participation in the study or the interpretation of results. This circumstance is expected to be exceptional, as the study aims to be as inclusive as possible.
Locations (1)
Hospital de la Santa Creu i Sant Pau, Barcelona, Barcelona 08041
Barcelona, Barcelona, Spain