Simple Meal Management Using Automated Insulin Delivery System

NCT06130215 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 34

Last updated 2024-04-25

No results posted yet for this study

Summary

Carbohydrate counting is an essential component of diabetes management in both adults and children, and together with an intensive insulin plan and increased blood glucose monitoring was associated with lower HbA1c. Carbohydrate counting is perceived as one of the most burdensome tasks in T1D and is frequently done inconsistently and with poor accuracy A recent analysis confirms that MiniMed™ Advaced Hybrid closed loop (AHCL) system is designed for optimal performance with meal announcement. Nonetheless, when meals containing \< 80 grams of carbohydrates are consumed with announcement of meals at will, there is a slight reduction in the number of daily boluses with no decline in glycemic control, yet markedly less diabetes related distress and improved treatment satisfaction TIR of 78.1% in unannounced meals compared with 78.8% with announced meals .

Conditions

Interventions

OTHER

Simple meal management

* Regular meal: Total Carbs per Day x 0.6 / 3 * Large meal: Total Carbs per Day x 0.6 / 3 x 1.5 * Small (Snack) meal: Total Carbs per Day x 0.6 / 3 x 1.5

OTHER

Precise meal management

precise carbohydrate counting for each meal

Sponsors & Collaborators

  • Sidra Medicine

    lead OTHER

Principal Investigators

  • Goran Petrovski, PhD · Sidra Medicine

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
12 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-15
Primary Completion
2024-06-30
Completion
2025-07-30

Countries

  • Qatar

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06130215 on ClinicalTrials.gov