Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
NCT04219709

Effects of Ketosis on Brain Function in Patients With T1DM

Led by Boston Children's Hospital · Updated on 2024-12-18

24

Participants Needed

1

Research Sites

343 weeks

Total Duration

On this page

Sponsors

B

Boston Children's Hospital

Lead Sponsor

B

Beth Israel Deaconess Medical Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

The scientific goal of this study is to examine the effects of a ketogenic diet on hypoglycemia tolerance and brain function in people with type 1 diabetes mellitus (T1D) and to clarify the mechanistic role of ketones in this process. Glycemic management of T1D is typified by alternating periods of hyper- and hypo-glycemia. Because brain metabolism under usual conditions depends on glucose, acute hypoglycemia leads to immediate complications including impaired cognitive function and a counter-regulatory hormone response. Recurrent hypoglycemia is associated with functional and structural changes in the brain and contributes to the cognitive decline observed in individuals with diabetes. The state of nutritional ketosis (as it occurs during fasting or when following a ketogenic \[very low carbohydrate\] diet) may protect against these acute and chronic complications. As the body relies on fat metabolism, ketone bodies build up and provide an alternative fuel for the brain. Studies during hypoglycemia have shown better cognitive function and less hypoglycemia symptoms in the setting of nutritional ketosis or with ketone administration. This physiological benefit may have special relevance for people with T1D who experience hypoglycemia frequently. To date, no mechanistic studies have examined brain effects of nutritional ketosis in T1D; nor have any trials explored the potential relevance of this for diabetes care.

CONDITIONS

Official Title

Effects of Ketosis on Brain Function in Patients With T1DM

Who Can Participate

Age: 18Years - 40Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Males and females with type 1 diabetes for at least 1 year
  • Age 18 to 40 years
  • Tanner stage IV or higher
  • Body mass index (BMI) between 18.5 and 35 kg/m2
  • Stable blood sugar control with HbA1c between 6.5% and 9%
  • Use of a continuous glucose monitor (CGM)
  • Use of an insulin pump
  • At least one diabetes care visit in the past 12 months (including virtual visits)
Not Eligible

You will not qualify if you...

  • Ketoacidosis or severe hypoglycemia with seizure or coma in the past 6 months
  • Dietary restrictions or intolerances incompatible with study foods, such as celiac disease, gastroparesis, or certain food allergies
  • Following a weight-loss or restrictive diet
  • Vigorous exercise more than 2 hours on more than 3 days per week
  • History or risk of eating disorder as assessed by the Eating Disorders Diagnostic Scale (EDDS)
  • Major medical illness or use of medications other than insulin and metformin that affect metabolism or blood sugar
  • Significant psychiatric illness
  • Smoking, recreational drug use, or excessive alcohol consumption
  • Pregnancy or breastfeeding
  • Anemia
  • For MRI participants: standard MRI exclusion criteria, irregular menstrual cycles, or use of psychotropic medications other than SSRIs or mild antidepressants/anxiety medications unless safely discontinued for MRI

AI-Screening

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Trial Site Locations

Total: 1 location

1

Boston Childrens Hospital

Boston, Massachusetts, United States, 02115

Actively Recruiting

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Research Team

B

Belinda Lennerz, MD PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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