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临床试验/NCT06687434
NCT06687434招募中不适用

Carb Counting vs. Simplified Qualitative Meal-Size Estimation- A Randomized Control Trial

Rabin Medical Center2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2024年12月15日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
120
试验地点
2
主要终点
Percentage of time in target range (70-18mg/dl)

研究概览

简要总结

The goal of this study is to compare qualitative meal-size estimation to accurate carb counting in adolescents with Type One Diabetes using all available AID (Automated Insulin Delivery) systems. We will compare glucose control parameters and patient related outcome measures between the groups. 120 children and adolescents with type 1 Diabetes who begin using AID system will be randomly assigned to one of two groups: simplified qualitative meal size estimation or accurate carb counting. The study will last 6 months, with an additional optional follow up points at 12 and 24 months.

In the first visit all patients will receive nutrition guidance from the dietitian. In the accurate carb counting group, participants will use precise carb counting to manage their meals. In the simplified qualitative meal-size estimation group, participants will use a simplified meal announcement based on three presets for each meal, small, medium, or large, which will be personalized based on the dietitian's assessment. During the study, the dietitian will evaluate the insulin-to-carb ratio and meal estimation at least once in the first two weeks.

Follow-up visits will be scheduled at 4-6 weeks, 3, and 6 months after the study's initiation. At each visit participants will upload their data from their AID systems. Evaluation of their diabetes control will be made and an assessment regarding the carbohydrates calculation method. Digital questionnaires assessing diabetes distress, disordered eating behaviors, dietary regimen, and eating patterns will be provided at the beginning of the study and after 6 months, with an additional optional follow-up points that will be held at 12 and 24 months after the study's initiation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
6 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • T1D- diagnosed
  • Age 6-18 years
  • Treated with insulin (multiple daily injections or pump) and intending to initiate treatment with AID systems

排除标准

  • Unstable medical conditions (other than diabetes) that may impact weight or diabetes management (as severe psychiatric disorders, various syndromes)
  • Use of medications that may impact weight or diabetes management (as use of steroids for an extended period of time. use of GLP-1)
  • Inability to understand the information, material and questionnaires of the study -

结局指标

主要结局

Percentage of time in target range (70-18mg/dl)

时间窗: Screening, after 4-6 weeks, after 3 months and after 6 months

Hemoglobin A1C

时间窗: Screening, after 4-6 weeks, after 3 months and after 6 months

Percentage Continuous glucose monitoting usage

时间窗: Screening, after 4-6 weeks, after 3 months and after 6 months

Number of Episodes of severe hypoglycemia

时间窗: Screening, after 4-6 weeks, after 3 months and after 6 months

Number of episodes of Diabetic Ketoacidosis

时间窗: Screening, after 4-6 weeks, after 3 months and after 6 months

次要结局

  • Total daily insulin dose(at screening, after 4-6 weeks, after 3 months and after 6 months.)
  • basal insulin dose(at screening, after 4-6 weeks, after 3 months and after 6 months.)
  • Number of manual boluses per day(at screening, after 4-6 weeks, after 3 months and after 6 months.)
  • Number of announced meals per day(at screening, after 4-6 weeks, after 3 months and after 6 months.)
  • Daily carbohydrates input(at screening, after 4-6 weeks, after 3 months and after 6 months.)
  • Percentage of automated insulin delivery use(at screening, after 4-6 weeks, after 3 months and after 6 months.)
  • Number of automated insulin delivery exits per week(at screening, after 4-6 weeks, after 3 months and after 6 months.)
  • Percentage of automated boluses(at screening, after 4-6 weeks, after 3 months and after 6 months.)
  • Score of Diabetes distress according to questionnaire(At screening and after 6 months)
  • Score of Disordered eating behaviors according to quesiotnnaire(At screening and after 6 months)
  • Score of Dietary regimen according to questionnaire(At screening and after 6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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