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Can Exogenous Ketone Supplementation Compensate for Glucose Hypometabolism and Improve Cognitive Processing Speed in Veterans With Prediabetes?

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Brief Summary The goal of this clinical trial is to learn whether older adults with prediabetes, but no diagnosed cognitive impairment, show early changes in brain energy use and thinking speed compared to older adults with normal blood sugar levels. The study will also test whether a single dose of an exogenous ketone supplement can improve brain energy use and cognitive processing speed. The main questions it aims to answer are: Do older adults with prediabetes have lower brain glucose uptake and slower cognitive processing speed compared to those with normal glucose levels? Does a single dose of an exogenous ketone monoester supplement improve cognitive processing speed and brain glucose uptake? Researchers will compare older adults with prediabetes to older adults with normal glucose levels to determine whether differences exist in brain glucose metabolism and cognitive performance. In a subset of participants, researchers will also compare brain and cognitive outcomes before and after consuming a ketone monoester supplement (DeltaG, Oxford, England). Participants will: Complete metabolic testing to determine glucose status Undergo brain imaging using fluorodeoxyglucose positron emission tomography combined with magnetic resonance imaging (18FDG-PET/MRI) while performing a cognitive processing speed task Consume a single dose of a commercially available ketone monoester supplement during one study visit Complete cognitive testing during imaging to measure processing speed and brain activity The results of this study will help determine whether early metabolic dysfunction is linked to reduced brain energy use and whether ketones can temporarily support brain function in individuals at risk for dementia.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 60
Maximum Age: 75
Healthy Volunteers: t
View:

• Age 60 to 75 years

• Able to provide written informed consent

• Fluent in English

• No diagnosed cognitive impairment or dementia

⁃ Classified as either:

• Prediabetes (based on American Diabetes Association criteria), or Normal glucose regulation (control group)

• Medically stable and cleared to undergo positron emission tomography and magnetic resonance imaging

• Willing to comply with study procedures, including metabolic testing, supplement ingestion, and neuroimaging

Locations
United States
Alabama
UAB Comprehensive Cancer Center
RECRUITING
Birmingham
Webb Nutrition Sciences Building
RECRUITING
Birmingham
Contact Information
Primary
Katherine Sweatt, PhD
sksweatt@uab.edu
205-975-5398
Time Frame
Start Date: 2025-05-20
Estimated Completion Date: 2027-05-31
Participants
Target number of participants: 20
Treatments
Experimental: Ketone
Placebo_comparator: Placebo
Related Therapeutic Areas
Sponsors
Leads: University of Alabama at Birmingham

This content was sourced from clinicaltrials.gov