CNP-103 in Adolescent and Adult Subjects Ages 12-35 With Recently Diagnosed (Within 6 Months) Stage 3 Type 1 Diabetes (T1D)
NCT06783309
Autoimmune Diseases, Diabetes Mellitus
Tucson, Arizona, United States
View Trial DetailsNCT Number: NCT07179471
Hybrid Closed Loop (HCL) systems, such as the MiniMed 780G, have significantly improved glycemic outcomes in Type 1 Diabetes (T1D) management. The MiniMed 780G, an Advanced Hybrid Closed Loop (AHCL) system, features autocorrection boluses and unique insulin adjustment technologies. While effective, the system requires user input for meal announcements. Some individuals attempt to "trick" the system by entering "fake carbs" to prompt additional insulin corrections. However, clinical evidence suggests this practice does not improve glycemic outcomes.
This study, conducted in Athens, Greece, will involve 40 children and adolescents (ages 7-18) with Type 1 Diabetes who have been using the MiniMed 780G system for over 6 months. The open-label, crossover design explores the impact of 'fake carbohydrates' on glycemic control. Participants will be split into two groups: one starts with 'fake carbohydrates' and then stops, while the other does the reverse. Over two weeks, their glycemic outcomes will be monitored and compared, with exclusions for severe diabetes complications or serious diabetic events
This study hypothesizes that using "fake carbs" does not enhance glycemic control. Findings are expected to provide evidence-based insights to optimize diabetes management and improve clinical guidance for HCL system users.
Interested in participating?
Request Info7 year–19 year
All sexes
Observational
Athens General Children's Hospital "Pan. & Aglaia Kyriakou", Athens, Attica, Greece
Aim of the Study To compare glycemic control outcomes in individuals with T1D using the MiniMed™ 780G system during periods when 'fake carbohydrates' are used versus periods when this strategy is not employed.
Definition: Fake Carbohydrates As a Fake Carbs practice is defined the practice when the user enters fake quantity of carbohydrates in order to trigger the system to suggest and deliver a bolus insulin with the aim to correct hyperglycemia.
Study Design and Participants This is a prospective, open-label, randomized, crossover trial conducted at the Diabetes Center of the General Hospital "P. & A. Kyriakou" in Athens, Greece.
Sample Size
Participants will be randomized into two groups based on their prior use of fake carbohydrates:
Group 1 (FC1): Continue using fake carbohydrates for 2 weeks, followed by discontinuation for 2 weeks.
Group 2 (FC2): Discontinue use of fake carbohydrates for 2 weeks, followed by resumption for 2 weeks.
Each intervention phase will be preceded by a 2-week run-in period to allow algorithm adaptation. A 2-week washout period between crossover phases will follow the same adaptation rationale.
Baseline and Ongoing Assessments
MiniMed™ 780G System Data
Review of pump settings during run-in phase
Settings optimized using:
Fake Carbohydrates Logbook
Participants will maintain a log recording:
Outcome Measures
Data Collection Tools CareLink™ Software: Used for glycemic data at baseline, week 2, and week 4 Participant logbooks for qualitative assessment of FC practices
Data Analysis Within-subject comparisons will be conducted due to crossover design Descriptive statistics for demographic and baseline characteristics Paired t-tests or Wilcoxon signed-rank tests for primary and secondary outcomes Repeated-measures ANOVA for longitudinal outcomes
Expected Impact This study will provide the first structured evaluation of the widely used but clinically unverified practice of entering 'fake carbohydrates' in AHCL systems. It will inform clinicians on whether this strategy improves or undermines glycemic control and support evidence-based recommendations for pump users and healthcare providers.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 2 weeks
Change between groups in blood glucose in Time in Range -TIR ( defined as 70-180 mg/dl) (%)
Time frame: 2 weeks
Change between groups in time in blood glucose in Tight Range -TITR ( defined as 70-140 mg/dl) (%)
Time frame: 2 weeks
Change between groups in blood glucose in Time Below Range- TBR (defined as <54mg/dl) (%)
Time frame: 2 weeks
Changes between groups in Glucose Management Indicator (GMI, %).
Time frame: 2 weeks
Changes between groups in blood glucose in Time Above Range (%)
Time frame: 2 weeks
Change between groups in mean sensor glucose (SG, mg/dl).
Time frame: 2 weeks
Changes between groups in Standard Deviation of glucose (SD, mg/dl)
Time frame: 2 weeks
Changes between groups in Coefficient of Variation for glucose (CV, %)
Time frame: 2 weeks
Changes between groups in number of announced carbs (gr/day)
Time frame: 2 weeks
Changes between groups in total daily insulin dose (TDD, units/day).
Time frame: 2 weeks
Changes between groups in insulin Auto-basal rate (%)
Time frame: 2 weeks
Changes between groups in insulin Auto-correction rate (%)
Time frame: 2 weeks
Changes between groups in insulin Manual bolus (%)
Time frame: 2 weeks
Changes between groups in number of severe hypoglycemia episodes, defined as as the ones requiring medical assistance.
Time frame: 2 weeks
Changes between the groups in the number of diabetic ketoacidosis (DKA) events , defined as:
Contact information is provided by the study sponsor or research team.
Maria Chatzipsalti
Other
"Fake Carbs" Practice in the Glycemic Outcomes in Children and Adolescents Using AID System: A Cross-over Observational Study
Acronym: CHeatAID
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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