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NCT Number: NCT06687434

Carb Counting vs. Simplified Qualitative Meal-Size Estimation

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.

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Key information

Age range

6 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Schneider Children's Medical Center

Petah Tikva, 4920235, Israel

Location status: Recruiting

Location contact

Alona Hamou, Msc

CONTACT

[email protected]

972-545-950277

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Non-T1D
  • 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 -

Treatment and study plan

accurate carb counting

Behavioral

Participants will use precise carb counting to manage their meals

Simplified qualitative meal size estimation

Behavioral

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.

Primary outcomes

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

    Time frame: Screening, after 4-6 weeks, after 3 months and after 6 months

  2. Hemoglobin A1C

    Time frame: Screening, after 4-6 weeks, after 3 months and after 6 months

  3. Percentage Continuous glucose monitoting usage

    Time frame: Screening, after 4-6 weeks, after 3 months and after 6 months

  4. Number of Episodes of severe hypoglycemia

    Time frame: Screening, after 4-6 weeks, after 3 months and after 6 months

  5. Number of episodes of Diabetic Ketoacidosis

    Time frame: Screening, after 4-6 weeks, after 3 months and after 6 months

Secondary outcomes

  1. Total daily insulin dose

    Time frame: at screening, after 4-6 weeks, after 3 months and after 6 months.

  2. basal insulin dose

    Time frame: at screening, after 4-6 weeks, after 3 months and after 6 months.

  3. Number of manual boluses per day

    Time frame: at screening, after 4-6 weeks, after 3 months and after 6 months.

  4. Number of announced meals per day

    Time frame: at screening, after 4-6 weeks, after 3 months and after 6 months.

  5. Daily carbohydrates input

    Time frame: at screening, after 4-6 weeks, after 3 months and after 6 months.

  6. Percentage of automated insulin delivery use

    Time frame: at screening, after 4-6 weeks, after 3 months and after 6 months.

  7. Number of automated insulin delivery exits per week

    Time frame: at screening, after 4-6 weeks, after 3 months and after 6 months.

  8. Percentage of automated boluses

    Time frame: at screening, after 4-6 weeks, after 3 months and after 6 months.

  9. Score of Diabetes distress according to questionnaire

    Time frame: At screening and after 6 months

  10. Score of Disordered eating behaviors according to quesiotnnaire

    Time frame: At screening and after 6 months

  11. Score of Dietary regimen according to questionnaire

    Time frame: At screening and after 6 months

Study contacts

Contact information is provided by the study sponsor or research team.

Michal Gilon Keren, Phd

CONTACT

[email protected]

972-524-311292

Tal Oron, DR.

CONTACT

[email protected]

972-544-290-296

Sponsors and collaborators

Lead sponsor

Rabin Medical Center

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Nov 13, 2024
Registry last updated
May 20, 2025

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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