Diabetes Mellitus, Type 1 Diabetes
Conditions
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
Study design
Eligibility
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
| Measure | Time frame | Description |
|---|---|---|
| Number of All Consented Participants | 4 months post-intervention | The capacity for recruitment was assessed, including all subjects that signed the Informed Consent Form (ICF). |
| Number of Participants That Completed All Visits | 4 months post-intervention | Number 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-intervention | 1 month post-intervention 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). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Caregiver Anxiety | Baseline, 1 month post-intervention, 4 months post-intervention | 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. |
| Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | 1 month post-intervention, 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. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| 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 |
| Total | 24 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Did not show up to the Follow-up appointment | 1 | 0 |
| Overall Study | Moved out of state | 0 | 2 |
Baseline characteristics
| Characteristic | Fixed Group | Insulin to Carbohydrate Ratio (ICR) Group | Total |
|---|---|---|---|
| Age, Continuous | 10 years | 11 years | 11 years |
| Ethnicity (NIH/OMB) Hispanic or Latino | 2 Participants | 2 Participants | 4 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 10 Participants | 10 Participants | 20 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Onset with Acidosis No | 4 Participants | 4 Participants | 8 Participants |
| Onset with Acidosis Yes | 8 Participants | 8 Participants | 16 Participants |
| Pubertal at onset No | 7 Participants | 7 Participants | 14 Participants |
| Pubertal at onset Yes | 5 Participants | 5 Participants | 10 Participants |
| Region of Enrollment United States | 12 participants | 12 participants | 24 participants |
| Sex: Female, Male Female | 5 Participants | 8 Participants | 13 Participants |
| Sex: Female, Male Male | 7 Participants | 4 Participants | 11 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 12 | 0 / 12 |
| other Total, other adverse events | 0 / 12 | 0 / 12 |
| serious Total, serious adverse events | 0 / 12 | 0 / 12 |
Outcome results
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
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Fixed Group | Caregiver Treatment Adherence at 1 Month and 4 Months Post-intervention | < 4 times/day at 1-month visit | 3.2 percentage of participants |
| Fixed Group | Caregiver Treatment Adherence at 1 Month and 4 Months Post-intervention | ≥ 4 times/day at 1-month visit | 96.8 percentage of participants |
| Fixed Group | Caregiver Treatment Adherence at 1 Month and 4 Months Post-intervention | < 4 times/day at 4-month visit | 2.6 percentage of participants |
| Fixed Group | Caregiver Treatment Adherence at 1 Month and 4 Months Post-intervention | ≥ 4 times/day at 4-month visit | 97.0 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Caregiver Treatment Adherence at 1 Month and 4 Months Post-intervention | ≥ 4 times/day at 4-month visit | 83.9 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Caregiver Treatment Adherence at 1 Month and 4 Months Post-intervention | < 4 times/day at 1-month visit | 10.2 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Caregiver Treatment Adherence at 1 Month and 4 Months Post-intervention | < 4 times/day at 4-month visit | 16.1 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Caregiver Treatment Adherence at 1 Month and 4 Months Post-intervention | ≥ 4 times/day at 1-month visit | 89.8 percentage of participants |
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Fixed Group | Number of All Consented Participants | 12 Participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Number of All Consented Participants | 12 Participants |
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Fixed Group | Number of Participants That Completed All Visits | 11 Participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Number of Participants That Completed All Visits | 10 Participants |
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.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Fixed Group | Caregiver Anxiety | Baseline | 29.1 score on a scale |
| Fixed Group | Caregiver Anxiety | 1 month post-intervention | 27.0 score on a scale |
| Fixed Group | Caregiver Anxiety | 4 months post-intervention | 27.6 score on a scale |
| Insulin to Carbohydrate Ratio (ICR) Group | Caregiver Anxiety | Baseline | 30.2 score on a scale |
| Insulin to Carbohydrate Ratio (ICR) Group | Caregiver Anxiety | 1 month post-intervention | 35.9 score on a scale |
| Insulin to Carbohydrate Ratio (ICR) Group | Caregiver Anxiety | 4 months post-intervention | 34.4 score on a scale |
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
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Fixed Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG 80-180 mg/dL at 4 month post-intervention | 63.3 percentage of participants |
| Fixed Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG < 50 mg/dL at 1 month post-intervention | 0.5 percentage of participants |
| Fixed Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG 80-180 mg/dL at 1 month post-intervention | 67.5 percentage of participants |
| Fixed Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG 50-79 mg/dL at 1 month post-intervention | 8.9 percentage of participants |
| Fixed Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG 181-350 mg/dL at 1 month post-intervention | 25.8 percentage of participants |
| Fixed Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG >350 mg/dL at 1 month post-intervention | 0.8 percentage of participants |
| Fixed Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG < 50 mg/dL at 4 month post-intervention | 0.0 percentage of participants |
| Fixed Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG 50-79 mg/dL at 4 month post-intervention | 8.6 percentage of participants |
| Fixed Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG 181-350 mg/dL at 4 month post-intervention | 28.7 percentage of participants |
| Fixed Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG >350 mg/dL at 4 month post-intervention | 0.1 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG 50-79 mg/dL at 4 month post-intervention | 7.3 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG 80-180 mg/dL at 4 month post-intervention | 69.0 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG >350 mg/dL at 1 month post-intervention | 0.3 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG < 50 mg/dL at 1 month post-intervention | 0.5 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG >350 mg/dL at 4 month post-intervention | 0.4 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG < 50 mg/dL at 4 month post-intervention | 0.4 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG 50-79 mg/dL at 1 month post-intervention | 8.3 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG 80-180 mg/dL at 1 month post-intervention | 63.2 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG 181-350 mg/dL at 4 month post-intervention | 21.8 percentage of participants |
| Insulin to Carbohydrate Ratio (ICR) Group | Glycemic Variability (GV) at 1 Month and 4 Months Post-intervention | BG 181-350 mg/dL at 1 month post-intervention | 26.8 percentage of participants |