search
Back to results

The Effects of a Low Carbohydrate, Non-Ketogenic Diet Versus Standard Diabetes Diet on Glycemic Control in Type 1 Diabetes (T1DLoCHO)

Primary Purpose

Diabetes Mellitus, Type 1

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Low carbohydrate diet
Standard of care diet
Sponsored by
University of Oklahoma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 1 focused on measuring Low carbohydrate diet

Eligibility Criteria

18 Years - 30 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Confirmed Type 1 diabetes for > 1 year confirmed by physician diagnosis
  • HbA1c >5.9% and <10%;
  • Confirmation of minimum three blood glucose tests per day (meter download or chart record)
  • Use of continuous subcutaneous insulin infusion therapy (CSII) or multiple daily injection (MDI) intensive insulin therapy
  • No change in insulin therapy type (CSII or MDI) in last 2 months or longer
  • Willingness to count carbohydrate and use bolus calculator on insulin pump during the intervention periods
  • Willingness to wear a 7 day CGM at three different time points during the study

Exclusion Criteria:

  • Females of childbearing potential who are pregnant or intend to become pregnant, are exclusively breastfeeding, or who are not using adequate contraceptive methods
  • Use of corticosteroids during or within 30 days prior to the intervention periods
  • Macroalbuminuria
  • Active proliferative retinopathy combined with an HbA1c ≥ 9%
  • Known or suspected alcohol or drug abuse
  • Other concomitant medical or psychological condition that according to the investigator's assessment makes the patient unsuitable for study participation

Sites / Locations

  • University of Oklahoma Harold Hamm Diabetes Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Experimental: Low carbohydrate diet

Experimental: Standard of care diet

Arm Description

Outcomes

Primary Outcome Measures

Time in Range
Difference in time spent with glucose values between 70-180 mg/dL assessed by continuous glucose monitoring (CGM)

Secondary Outcome Measures

Mean Glucose
Difference in mean glucose values assessed by CGM
Standard deviation of glucose
Difference in standard deviation of glucose values assessed by CGM
Mean amplitude of glycemic excursions
Difference in mean amplitude of glycemic excursions assessed by CGM
Time in hypoglycemia
Difference in time spent with glucose values <70 mg/dL; between 55-70 mg/dL; and <55 mg/dL
Time in hyperglycemia
Difference in time spent with glucose values >180 mg/dL
Change in HbA1c
Difference in change in hemoglobin A1c
Coefficient of Variation
Estimate of glucose variability calculated by dividing the standard deviation by average glucose
Severe hypoglycemia
Difference in number of severe hypoglycemia episodes (glucagon or IV dextrose administration)
Total daily insulin dose
Difference in total daily insulin dose
Total daily basal insulin 24 hour
Difference in total daily basal insulin in 24 hours
Total daily bolus insulin 24 hour
Difference in total daily bolus insulin in 24 hours
Body weight
Change in body weight
Body Mass Index (BMI)
Change in BMI
Systolic Blood Pressure (mm Hg)
Change in systolic BP
Diastolic Blood Pressure (mm Hg)
Change in diastolic BP
Pulse, per minute
Change in pulse
Energy Intake (kcal/day)
Change in energy intake
Daily carbohydrate intake (total carbohydrate, g/day)
Change in carbohydrate intake
Percent energy intake as Carbohydrate
Change in % carbohydrate intake
Daily protein intake (total protein, g/day) and Daily fat intake (total fat, g/day)
Change in protein intake
Fat quality intake (% total fat as monounsaturated, polyunsaturated, saturated, omega-3)
Change in fat quality
Standard Lipid Panel
Change in (Total cholesterol, HDL cholesterol, LDL cholesterol-calculated, triglycerides; mg/dL)
LDL-P (nmol/L)
Change in LDL-P
HDL-P (umol/L)
Change in HDL-P
VLDL-P
Change in VLDL-P (nmol/L)
LDL size
Change in LDL size (nm)
HDL size
Change in HDL size (nm)
VLDL size
Change in VLDL size (nm)
High-sensitive C-reactive protein (hs-CRP)
Change in hs-CRP
Plasma lipopolysaccharide
Surrogate marker for inflammation
Serum Ketones (beta-hydroxybutyrate)
beta-hydroxybutyrate (mmol/L)
Type 1 Diabetes Nutrition Knowledge Survey
Validated nutrition knowledge survey (nutrition label reading, carbohydrate counting)
Diet Quality
Minerals, Vitamins, Dietary Fiber amounts compared to DRIs for age, ascertained by 3 day 24 hour food logs

Full Information

First Posted
May 7, 2018
Last Updated
January 9, 2020
Sponsor
University of Oklahoma
search

1. Study Identification

Unique Protocol Identification Number
NCT03544892
Brief Title
The Effects of a Low Carbohydrate, Non-Ketogenic Diet Versus Standard Diabetes Diet on Glycemic Control in Type 1 Diabetes
Acronym
T1DLoCHO
Official Title
The Effects of a Low Carbohydrate, Non-Ketogenic Diet Versus Standard Diabetes Diet on Glycemic Control in Type 1 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Terminated
Why Stopped
PI left the University; study will not continue.
Study Start Date
May 1, 2018 (Actual)
Primary Completion Date
June 28, 2019 (Actual)
Study Completion Date
June 28, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Oklahoma

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This randomized, crossover nutrition intervention seeks to examine the effects of a non-ketogenic low carbohydrate (CHO) diet (60-80g per day) on glycemic control, lipids, and markers on inflammation in individuals with Type 1 Diabetes (T1D). This study will be used to inform clinical practice, especially in teaching medical nutrition therapy to new-onset diabetes patients and those struggling with glycemic control and hyperlipidemia. At this time, no evidenced-based universal recommendations from randomized controlled trials exist to support low carbohydrate dietary patterns as a front-line approach in individuals with T1D. The investigators hypothesize a diet consisting of 60-80 g carbohydrate diet will result in greater improvement in glycemic control compared to a 50% carbohydrate diet in patients with Type 1 diabetes over 12 weeks in the outpatient setting.
Detailed Description
Type 1 diabetes mellitus (T1D) is marked by total insulin dependence with challenges regarding glycemic control and concomitant sequela. While standard of care medical nutrition therapy for this disease centers on matching carbohydrate to insulin at meals, recent literature and clinical reports have shown superior glycemic control and cardiovascular measures with lower carbohydrate dietary patterns (<130g/day) as compared to the standard American MyPlate (50% total calories as carbohydrate) approach. Diabetes management has evolved tremendously in the last twenty years with the development of sophisticated insulin pumps and continuous glucose monitors; but, glycemic control is still dependent on quantification of carbohydrate, imperfect in the real-world setting. Due to inherent error in carbohydrate counting, the investigators propose that less carbohydrate will produce better glycemic control by minimizing error and subsequent variation in individuals with type 1 diabetes. There has long been a movement in the medical community to prescribe low carbohydrate diets under the premise of "less carbohydrate, less insulin, less glycemic variation". This strategy centers on "the law of small numbers", a calculus principle describing magnitude of variation in the output (glycemic variation) as the function of input size (CHO + insulin). Carbohydrate counting tends to result in ~50% error while there is ~30% variation in insulin action, making exactitude impossible. However, low CHO diets tend to provide >40% energy from fat due to the macronutrient distribution. With innate risk of cardiovascular disease in T1D, standard of care has supported restriction of total fat consumption, especially saturated fat, in effort to control cholesterol. While the American Diabetes Association recognizes that dietary fat is a controversial and complex issue, eliminating trans-fats is the only consensus point across the field. To date, most low CHO diet studies in both T1D and Type 2 Diabetes (T2D) have not shown adverse effects on lipids and tend to show decreases in triglycerides and either no change or increases in HDL, LDL, and total cholesterol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 1
Keywords
Low carbohydrate diet

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
This study uses 33 week randomized, powered study design to measure glycemic control with a low carbohydrate dietary pattern versus standard of care diabetes medical nutrition therapy. Each arm is 12 weeks with an 8 week washout between arms.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
11 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Experimental: Low carbohydrate diet
Arm Type
Experimental
Arm Title
Experimental: Standard of care diet
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
Low carbohydrate diet
Intervention Description
60-80 g total carbohydrate per day
Intervention Type
Other
Intervention Name(s)
Standard of care diet
Intervention Description
> 150 g total carbohydrate per day
Primary Outcome Measure Information:
Title
Time in Range
Description
Difference in time spent with glucose values between 70-180 mg/dL assessed by continuous glucose monitoring (CGM)
Time Frame
5 days of worn CGM during each intervention
Secondary Outcome Measure Information:
Title
Mean Glucose
Description
Difference in mean glucose values assessed by CGM
Time Frame
Baseline to 12 weeks (1 week worn CGM data)
Title
Standard deviation of glucose
Description
Difference in standard deviation of glucose values assessed by CGM
Time Frame
Baseline to 12 weeks (1 week worn CGM data)
Title
Mean amplitude of glycemic excursions
Description
Difference in mean amplitude of glycemic excursions assessed by CGM
Time Frame
Baseline to 12 weeks (1 week worn CGM data)
Title
Time in hypoglycemia
Description
Difference in time spent with glucose values <70 mg/dL; between 55-70 mg/dL; and <55 mg/dL
Time Frame
Baseline to 12 weeks (1 week worn CGM data)
Title
Time in hyperglycemia
Description
Difference in time spent with glucose values >180 mg/dL
Time Frame
Baseline to 12 weeks (1 week worn CGM data)
Title
Change in HbA1c
Description
Difference in change in hemoglobin A1c
Time Frame
Baseline to 12 weeks
Title
Coefficient of Variation
Description
Estimate of glucose variability calculated by dividing the standard deviation by average glucose
Time Frame
Baseline to 12 weeks (1 week worn CGM data)
Title
Severe hypoglycemia
Description
Difference in number of severe hypoglycemia episodes (glucagon or IV dextrose administration)
Time Frame
Baseline to 12 weeks
Title
Total daily insulin dose
Description
Difference in total daily insulin dose
Time Frame
Baseline to 12 weeks
Title
Total daily basal insulin 24 hour
Description
Difference in total daily basal insulin in 24 hours
Time Frame
Baseline to 12 weeks
Title
Total daily bolus insulin 24 hour
Description
Difference in total daily bolus insulin in 24 hours
Time Frame
Baseline to 12 weeks
Title
Body weight
Description
Change in body weight
Time Frame
Baseline to 12 weeks
Title
Body Mass Index (BMI)
Description
Change in BMI
Time Frame
Baseline to 12 weeks
Title
Systolic Blood Pressure (mm Hg)
Description
Change in systolic BP
Time Frame
Baseline to 12 weeks
Title
Diastolic Blood Pressure (mm Hg)
Description
Change in diastolic BP
Time Frame
Baseline to 12 weeks
Title
Pulse, per minute
Description
Change in pulse
Time Frame
Baseline to 12 weeks
Title
Energy Intake (kcal/day)
Description
Change in energy intake
Time Frame
Baseline to 12 weeks
Title
Daily carbohydrate intake (total carbohydrate, g/day)
Description
Change in carbohydrate intake
Time Frame
Baseline to 12 weeks
Title
Percent energy intake as Carbohydrate
Description
Change in % carbohydrate intake
Time Frame
Baseline to 12 weeks
Title
Daily protein intake (total protein, g/day) and Daily fat intake (total fat, g/day)
Description
Change in protein intake
Time Frame
Baseline to 12 weeks
Title
Fat quality intake (% total fat as monounsaturated, polyunsaturated, saturated, omega-3)
Description
Change in fat quality
Time Frame
Baseline to 12 weeks
Title
Standard Lipid Panel
Description
Change in (Total cholesterol, HDL cholesterol, LDL cholesterol-calculated, triglycerides; mg/dL)
Time Frame
Baseline to 12 weeks
Title
LDL-P (nmol/L)
Description
Change in LDL-P
Time Frame
Baseline to 12 weeks
Title
HDL-P (umol/L)
Description
Change in HDL-P
Time Frame
Baseline to 12 weeks
Title
VLDL-P
Description
Change in VLDL-P (nmol/L)
Time Frame
Baseline to 12 weeks
Title
LDL size
Description
Change in LDL size (nm)
Time Frame
Baseline to 12 weeks
Title
HDL size
Description
Change in HDL size (nm)
Time Frame
Baseline to 12 weeks
Title
VLDL size
Description
Change in VLDL size (nm)
Time Frame
Baseline to 12 weeks
Title
High-sensitive C-reactive protein (hs-CRP)
Description
Change in hs-CRP
Time Frame
Baseline to 12 weeks
Title
Plasma lipopolysaccharide
Description
Surrogate marker for inflammation
Time Frame
Baseline to 12 weeks
Title
Serum Ketones (beta-hydroxybutyrate)
Description
beta-hydroxybutyrate (mmol/L)
Time Frame
Baseline to 12 weeks
Title
Type 1 Diabetes Nutrition Knowledge Survey
Description
Validated nutrition knowledge survey (nutrition label reading, carbohydrate counting)
Time Frame
Baseline to Week 33 (end of study)
Title
Diet Quality
Description
Minerals, Vitamins, Dietary Fiber amounts compared to DRIs for age, ascertained by 3 day 24 hour food logs
Time Frame
Baseline to 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Confirmed Type 1 diabetes for > 1 year confirmed by physician diagnosis HbA1c >5.9% and <10%; Confirmation of minimum three blood glucose tests per day (meter download or chart record) Use of continuous subcutaneous insulin infusion therapy (CSII) or multiple daily injection (MDI) intensive insulin therapy No change in insulin therapy type (CSII or MDI) in last 2 months or longer Willingness to count carbohydrate and use bolus calculator on insulin pump during the intervention periods Willingness to wear a 7 day CGM at three different time points during the study Exclusion Criteria: Females of childbearing potential who are pregnant or intend to become pregnant, are exclusively breastfeeding, or who are not using adequate contraceptive methods Use of corticosteroids during or within 30 days prior to the intervention periods Macroalbuminuria Active proliferative retinopathy combined with an HbA1c ≥ 9% Known or suspected alcohol or drug abuse Other concomitant medical or psychological condition that according to the investigator's assessment makes the patient unsuitable for study participation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christina M Crowder, RDN, CNSC, LD
Organizational Affiliation
University of Oklahoma
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Oklahoma Harold Hamm Diabetes Center
City
Tulsa
State/Province
Oklahoma
ZIP/Postal Code
74135
Country
United States

12. IPD Sharing Statement

Learn more about this trial

The Effects of a Low Carbohydrate, Non-Ketogenic Diet Versus Standard Diabetes Diet on Glycemic Control in Type 1 Diabetes

We'll reach out to this number within 24 hrs