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A Study of Rapid-Acting Mealtime Insulin in Children and Adolescents With Newly Diagnosed Type 1 Diabetes Mellitus

Fixed Dose for Fixed Carbohydrates vs. Variable Dosing for Variable Carbohydrates: A Study of Rapid-Acting Mealtime Insulin in Children and Adolescents With Newly Diagnosed Type 1 Diabetes Mellitus.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04157738
Enrollment
24
Registered
2019-11-08
Start date
2019-11-27
Completion date
2020-12-17
Last updated
2021-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Type 1 Diabetes

Keywords

Diabetes, Glycemic variability, Insulin, Parental Stress, Advanced carbohydrates counting, Insulin for meals

Brief summary

Type 1 diabetes mellitus (T1DM) is a challenging medical disorder, especially in children and adolescents. In order to prevent the chronic complications of hyperglycemia, the maintenance of near-normal glycemic control must be balanced with minimizing hypoglycemia. Although many pediatric endocrinologists provide an ICR plan for their newly diagnosed patients with T1DM, fixed dosing and other forms of insulin delivery are available. This proposal is designed to compare children and adolescents with newly diagnosed T1DM using a fixed insulin dose for fixed carbohydrate mealtime regimen (FIXED group) to children and adolescents with newly diagnosed T1DM using an ICR with variable carbohydrate intake (ICR group) mealtime regimen. In addition to determining the feasibility for a subsequently larger clinical trial, the aims of this investigator-initiated, prospective proposal, is twofold. The first is to determine if the caregivers of diabetics using a fixed insulin for fixed carbohydrate regimen (FIXED group) experience less anxiety than the caregivers of those using an ICR with variable carbohydrate intake regimen (ICR group) at 1- and 4-months post-randomization. The second is to determine if diabetics utilizing a fixed insulin for fixed carbohydrate regimen (FIXED group) have decreased glycemic variability (GV) than those using an ICR with variable carbohydrate intake regimen (ICR group) at 1- and 4-months post-randomization.

Detailed description

Although children and adolescents with T1DM have much more freedom with the amount of food (carbohydrates) they eat while using an ICR at mealtime, the difficulty in determining the amount of insulin needed, how and when to adjust the ICR, the difficulty with understanding the basics of managing T1DM, and the adaptation to a new lifestyle with T1DM may be more complicated than utilizing a simple plan that includes a fixed amount of insulin and fixed number of carbohydrates, at least for the first few months after diagnosis. As complicated as it is for children, adolescents, and their caregivers to learn how to manage T1DM after being discharged home in usually \< 48 hours after diagnosis, a more simplified insulin regimen at mealtime may provide the family of and the child or adolescent with newly diagnosed T1DM with less stress and anxiety while still maintaining adequate glycemic control. Twenty - 40 subjects will be recruited at Children's Hospital of Atlanta (CHOA) at Egleston and will be randomized to either the FIXED group or the ICR group according to a computer-generated random sampling table. The subject and his/her caregivers will receive diabetes education while in the hospital in standard fashion. The subject and his/her caregivers will receive glucose monitoring education and training prior to hospital discharge. The subject and his/her caregivers will also receive a paper log to record the blood sugars, number of carbohydrates consumed and insulin administered at each meal throughout the day. Prior to discharge, all subjects will receive a regimen that includes a: 1) Meal-time insulin and carbohydrate regimen (# of units of insulin, # of carbohydrates, and/or ICR); 2) Daily dose of Glargine; 3) Hyperglycemia correction regimen for blood glucose levels \> 199 mg/dL; and 4) Hypoglycemia treatment regimen for blood glucose levels \< 70 mg/dL and/or symptomatic. As per standard diabetes care, caregivers will report all blood glucose levels every day (to the study investigators) until the subject's initial clinic visit 4-6 weeks after diagnosis. All insulin adjustments will be made by the study investigators. After the subject's first clinic visit, caregivers will contact the study investigators once a week to report blood glucose levels and the investigators will make adjustments as needed. All the diabetes clinic visits will occur at the Center for Advanced Pediatrics (CAP), approximately three miles from CHOA-Egleston Hospital. Subjects will attend clinic with one or more of the investigators approximately 1 and 4 months after enrollment. At each clinic visit, subjects (and their caregivers) will answer standard diabetes questions, subjects will undergo a physical examination, and subjects' objective data (vital signs, glucose meter (GM) data, insulin dosing, and carbohydrate intake) will be collected by the study personnel.

Interventions

Prior to discharge, all subjects will receive a regimen that includes a Meal-time insulin and carbohydrate regimen (number of units of insulin, number of carbohydrates, and/or ICR)

Prior to discharge, all subjects will receive a regimen that includes a daily dose of long-acting insulin (Glargine)

Sponsors

Emory University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Years to 15 Years
Healthy volunteers
No

Inclusion criteria

* Have Confirmed diagnosis of T1DM based on the most recent ADA criteria * Be 7 - 15 years of age * Begin monitoring with a glucose monitor prior to discharge from the hospital * Have the ability to understand and be willing to adhere to the study protocol * English or Spanish speakers

Exclusion criteria

* Have a clinically significant major organ system disease * Be on glucocorticoid therapy * Have Type 2 Diabetes Mellitus * Have Polycystic Ovarian Syndrome (PCOS) * Have a BMI \> 85th %ile * Have Acanthosis Nigricans * Have any form of renal impairment * Have Cystic Fibrosis * Have Glucocorticoid-, Chemotherapeutic-, or any other Medication-induced form of Diabetes * Be using any basal insulin other than Glargine insulin * Have cognitive impairment (\> 2 grades behind age-appropriate grade in school) * Be in Foster Care * Have any history of Division of Family and Children Services (DFCS) involvement * If female, be pregnant or breast-feeding.

Design outcomes

Primary

MeasureTime frameDescription
Number of All Consented Participants4 months post-interventionThe capacity for recruitment was assessed, including all subjects that signed the Informed Consent Form (ICF).
Number of Participants That Completed All Visits4 months post-interventionNumber of participants that were able to complete all study visits, including the visits in-person at 1 month and 4 months post-randomization.
Caregiver Treatment Adherence at 1 Month and 4 Months Post-intervention1 month post-intervention and 4 months post-interventionCaregiver treatment adherence was assessed using a blood glucose log. Subjects and caregivers recorded blood glucose levels and the amount/type of insulin given. This data was used to calculate adherence as a percentage ranging from 0% (no adherence) to 100% (full adherence).

Secondary

MeasureTime frameDescription
Caregiver AnxietyBaseline, 1 month post-intervention, 4 months post-interventionCaregiver anxiety was measured with the parental stress scale. Caregivers completed the parental stress scale at initial enrollment and at each clinic follow up visit. The Parental Stress Scale includes 18 questions that are rated from 1 (strongly disagree) to 5 (strongly agree). Scoring ranges from 18 - 90. The higher the score, the higher the stress and anxiety level.
Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention1 month post-intervention, 4 months post-interventionThe GV was calculated in all subjects using the average blood glucose levels collected from the daily blood glucose paper log. A subjective qualification system was used to label each subject's GV based on their blood glucose levels and an established glucose monitoring (GM) data system. Subjects are considered to have appropriate GV if their blood glucose levels are in the range of 80 mg/dL - 180 mg/dL. Percentage of participants within each specific average BG range is shown.

Countries

United States

Participant flow

Participants by arm

ArmCount
Fixed Group
Children and adolescents with newly-diagnosed T1DM will receive a fixed mealtime carbohydrate with a fixed mealtime insulin dose, that is a simplified regimen that provides a set amount of insulin for a set amount of carbohydrates, and ensures that each dose and each meal is consistent. Rapid-Acting Insulin: Prior to discharge, all subjects will receive a regimen that includes a Meal-time insulin and carbohydrate regimen (number of units of insulin, number of carbohydrates, and/or ICR) Long acting insulin: Prior to discharge, all subjects will receive a regimen that includes a daily dose of long-acting insulin (Glargine)
12
Insulin to Carbohydrate Ratio (ICR) Group
Children and adolescents with newly-diagnosed T1DM will receive an Insulin to carbohydrate ratio (ICR) with variable carbohydrate intake mealtime regimen Rapid-Acting Insulin: Prior to discharge, all subjects will receive a regimen that includes a Meal-time insulin and carbohydrate regimen (number of units of insulin, number of carbohydrates, and/or ICR) Long acting insulin: Prior to discharge, all subjects will receive a regimen that includes a daily dose of long-acting insulin (Glargine)
12
Total24

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyDid not show up to the Follow-up appointment10
Overall StudyMoved out of state02

Baseline characteristics

CharacteristicFixed GroupInsulin to Carbohydrate Ratio (ICR) GroupTotal
Age, Continuous10 years11 years11 years
Ethnicity (NIH/OMB)
Hispanic or Latino
2 Participants2 Participants4 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
10 Participants10 Participants20 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Onset with Acidosis
No
4 Participants4 Participants8 Participants
Onset with Acidosis
Yes
8 Participants8 Participants16 Participants
Pubertal at onset
No
7 Participants7 Participants14 Participants
Pubertal at onset
Yes
5 Participants5 Participants10 Participants
Region of Enrollment
United States
12 participants12 participants24 participants
Sex: Female, Male
Female
5 Participants8 Participants13 Participants
Sex: Female, Male
Male
7 Participants4 Participants11 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 120 / 12
other
Total, other adverse events
0 / 120 / 12
serious
Total, serious adverse events
0 / 120 / 12

Outcome results

Primary

Caregiver Treatment Adherence at 1 Month and 4 Months Post-intervention

Caregiver treatment adherence was assessed using a blood glucose log. Subjects and caregivers recorded blood glucose levels and the amount/type of insulin given. This data was used to calculate adherence as a percentage ranging from 0% (no adherence) to 100% (full adherence).

Time frame: 1 month post-intervention and 4 months post-intervention

ArmMeasureGroupValue (NUMBER)
Fixed GroupCaregiver Treatment Adherence at 1 Month and 4 Months Post-intervention< 4 times/day at 1-month visit3.2 percentage of participants
Fixed GroupCaregiver Treatment Adherence at 1 Month and 4 Months Post-intervention≥ 4 times/day at 1-month visit96.8 percentage of participants
Fixed GroupCaregiver Treatment Adherence at 1 Month and 4 Months Post-intervention< 4 times/day at 4-month visit2.6 percentage of participants
Fixed GroupCaregiver Treatment Adherence at 1 Month and 4 Months Post-intervention≥ 4 times/day at 4-month visit97.0 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupCaregiver Treatment Adherence at 1 Month and 4 Months Post-intervention≥ 4 times/day at 4-month visit83.9 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupCaregiver Treatment Adherence at 1 Month and 4 Months Post-intervention< 4 times/day at 1-month visit10.2 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupCaregiver Treatment Adherence at 1 Month and 4 Months Post-intervention< 4 times/day at 4-month visit16.1 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupCaregiver Treatment Adherence at 1 Month and 4 Months Post-intervention≥ 4 times/day at 1-month visit89.8 percentage of participants
Primary

Number of All Consented Participants

The capacity for recruitment was assessed, including all subjects that signed the Informed Consent Form (ICF).

Time frame: 4 months post-intervention

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Fixed GroupNumber of All Consented Participants12 Participants
Insulin to Carbohydrate Ratio (ICR) GroupNumber of All Consented Participants12 Participants
Primary

Number of Participants That Completed All Visits

Number of participants that were able to complete all study visits, including the visits in-person at 1 month and 4 months post-randomization.

Time frame: 4 months post-intervention

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Fixed GroupNumber of Participants That Completed All Visits11 Participants
Insulin to Carbohydrate Ratio (ICR) GroupNumber of Participants That Completed All Visits10 Participants
Secondary

Caregiver Anxiety

Caregiver anxiety was measured with the parental stress scale. Caregivers completed the parental stress scale at initial enrollment and at each clinic follow up visit. The Parental Stress Scale includes 18 questions that are rated from 1 (strongly disagree) to 5 (strongly agree). Scoring ranges from 18 - 90. The higher the score, the higher the stress and anxiety level.

Time frame: Baseline, 1 month post-intervention, 4 months post-intervention

Population: Number of participants analyzed include subjects that had visits in-person at 1 month and 4 months post-randomization.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Fixed GroupCaregiver AnxietyBaseline29.1 score on a scale
Fixed GroupCaregiver Anxiety1 month post-intervention27.0 score on a scale
Fixed GroupCaregiver Anxiety4 months post-intervention27.6 score on a scale
Insulin to Carbohydrate Ratio (ICR) GroupCaregiver AnxietyBaseline30.2 score on a scale
Insulin to Carbohydrate Ratio (ICR) GroupCaregiver Anxiety1 month post-intervention35.9 score on a scale
Insulin to Carbohydrate Ratio (ICR) GroupCaregiver Anxiety4 months post-intervention34.4 score on a scale
Secondary

Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention

The GV was calculated in all subjects using the average blood glucose levels collected from the daily blood glucose paper log. A subjective qualification system was used to label each subject's GV based on their blood glucose levels and an established glucose monitoring (GM) data system. Subjects are considered to have appropriate GV if their blood glucose levels are in the range of 80 mg/dL - 180 mg/dL. Percentage of participants within each specific average BG range is shown.

Time frame: 1 month post-intervention, 4 months post-intervention

ArmMeasureGroupValue (NUMBER)
Fixed GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG 80-180 mg/dL at 4 month post-intervention63.3 percentage of participants
Fixed GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG < 50 mg/dL at 1 month post-intervention0.5 percentage of participants
Fixed GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG 80-180 mg/dL at 1 month post-intervention67.5 percentage of participants
Fixed GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG 50-79 mg/dL at 1 month post-intervention8.9 percentage of participants
Fixed GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG 181-350 mg/dL at 1 month post-intervention25.8 percentage of participants
Fixed GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG >350 mg/dL at 1 month post-intervention0.8 percentage of participants
Fixed GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG < 50 mg/dL at 4 month post-intervention0.0 percentage of participants
Fixed GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG 50-79 mg/dL at 4 month post-intervention8.6 percentage of participants
Fixed GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG 181-350 mg/dL at 4 month post-intervention28.7 percentage of participants
Fixed GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG >350 mg/dL at 4 month post-intervention0.1 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG 50-79 mg/dL at 4 month post-intervention7.3 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG 80-180 mg/dL at 4 month post-intervention69.0 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG >350 mg/dL at 1 month post-intervention0.3 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG < 50 mg/dL at 1 month post-intervention0.5 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG >350 mg/dL at 4 month post-intervention0.4 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG < 50 mg/dL at 4 month post-intervention0.4 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG 50-79 mg/dL at 1 month post-intervention8.3 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG 80-180 mg/dL at 1 month post-intervention63.2 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG 181-350 mg/dL at 4 month post-intervention21.8 percentage of participants
Insulin to Carbohydrate Ratio (ICR) GroupGlycemic Variability (GV) at 1 Month and 4 Months Post-interventionBG 181-350 mg/dL at 1 month post-intervention26.8 percentage of participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026