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The Efficacy of MDI Treatment With an Optimization Algorithm Adjusting Basal-Bolus Parameters in Children and Adolescents With Type 1 Diabetes at a Diabetes Camp

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McGill University

Status

Completed

Conditions

Diabetes Mellitus, Type 1
Diabete Mellitus

Treatments

Other: Multiple Daily Injections: Slow acting insulin and Rapid acting insulin

Study type

Interventional

Funder types

Other

Identifiers

NCT03764280
MDI Optimization Algorithm

Details and patient eligibility

About

Our lab at McGill University has developed an optimization algorithm for T1D MDI patients that estimates optimal basal-bolus parameters (basal injections and insulin-to-carbohydrate ratios) using glucose sensor data and insulin dosing data over several days. The algorithm examines daily glucose, insulin, and meal data to make changes in patients' basal injections and ICRs. The investigators hope that this algorithm will be able to optimize the patients' individual basal injections and ICRs in order to improve glycemic control.

Full description

The objective of this project is to compare our basal-bolus optimization algorithm with physician adjusted basal-bolus parameters using a randomized parallel clinical trial in children and adolescents at a Camp Carowanis. The investigators hypothesize that using this optimization algorithm will be non-inferior to the physician-adjusted basal-bolus parameters regarding time spent in target glucose range (3.9 mmol/L - 10mmol/L).

Between 40 and 68 children and adolescent type 1 diabetes patients undergoing MDI treatment at Camp Carowanis will randomly undergo one of two interventions:

  1. MDI with Physician Adjusted Basal-Bolus Parameters: Participants will be wearing the Freestyle Libre glucose sensor (Abbott Diabetes Care). Participants will undergo their conventional multiple daily injection (MDI) therapy. At breakfast, the research team will download the sensor data. Camp physicians will review each participant's sensor and insulin data and make changes to their parameters based on their clinical judgement, as they would for all campers, regardless of study participation. These new parameters will be entered into the patient's camp file.
  2. MDI with Basal-Bolus Optimization Algorithm Adjusted Basal-Bolus Parameters: Participants will be wearing the Freestyle Libre glucose sensor (Abbott Diabetes Care). At breakfast, the data from the glucose sensor and injection information will be entered into a computer and the optimization algorithm will be run. Camp physicians will review the algorithm's recommendations before they are entered into the patient's camp file.

Enrollment

21 patients

Sex

All

Ages

8 to 21 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Males and females between 8 and 18 years old.
  2. Clinical diagnosis of type 1 diabetes for at least 12 months. The diagnosis of type 1 diabetes is based on the investigator's judgment; C peptide level and antibody determinations are not needed.
  3. Undergoing multiple daily injection therapy.
  4. HbA1c ≤ 11%.

Exclusion criteria

  1. Serious medical illness likely to interfere with study participation or with the ability to complete the trial by the judgment of the investigator.
  2. Failure to comply with the study protocol or with team's recommendations.
  3. Injection of isophane insulin (NPH) or any intermediate-acting insulin
  4. More than one injection of slow-acting insulin per day.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

21 participants in 2 patient groups

MDI with Physician Adjusted Basal-Bolus Parameters
No Intervention group
Description:
Participants will be wearing the Freestyle Libre glucose sensor (Abbott Diabetes Care). Participants will undergo their conventional multiple daily injection (MDI) therapy.
MDI with Basal-Bolus Optimization Algorithm
Experimental group
Description:
Participants will be wearing the Freestyle Libre glucose sensor (Abbott Diabetes Care). Once daily, the data from the glucose sensor and injection information will be entered into a computer and the optimization algorithm will be run. Once daily, participants' parameters may be changed based on the algorithm's recommendations.
Treatment:
Other: Multiple Daily Injections: Slow acting insulin and Rapid acting insulin

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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