Recruiting

Cerebral Lactate Uptake in Obese and Non-Obese Individuals

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Behavior+11

+ Body Weight

+ Diabetes Mellitus

From 18 to 45 Years
+9 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Other

Utilizing specific methods not covered by standard models in order to address unique research questions.
Observational
Study Start: May 2025
See protocol details

Summary

Principal SponsorUniversity of Missouri-Columbia
Study ContactMatt McDonald, MSMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: May 1, 2025

Actual date on which the first participant was enrolled.

The study aims to understand how the brain uses lactate, a byproduct of metabolism, in both obese and non-obese individuals. While lactate is often thought of as just a waste product, it actually plays important roles in the body, including being a source of energy and acting as a signaling molecule. The study focuses on how well the brain can use lactate when it is stressed, which may be different for those with obesity or type 2 diabetes due to possible issues in their lactate metabolism. This research is important because it might reveal new insights into brain function under stress and how obesity affects this process. Participants in this study will undergo an exercise stress test and engage in submaximal exercise, which is less intense than maximal effort. During these activities, researchers will measure the brain's blood flow using a technique called transcranial doppler, which is a non-invasive way to observe how blood moves through the brain. The study will compare these measurements between obese and non-obese participants to see if there are any differences in how their brains respond to lactate during exercise. Understanding these differences could lead to better strategies for managing conditions like obesity and type 2 diabetes.

Official TitleCerebral Lactate Uptake and Transport in Obese and Non-Obese Individuals
Principal SponsorUniversity of Missouri-Columbia
Study ContactMatt McDonald, MSMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

24 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Other

Some studies use unique or mixed approaches that don't fit standard categories. These may include innovative observational methods or studies tailored to specific research questions.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 45 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

BehaviorBody WeightDiabetes MellitusEndocrine System DiseasesMetabolic DiseasesMotor ActivityNutrition DisordersNutritional and Metabolic DiseasesObesitySigns and SymptomsPathological Conditions, Signs and SymptomsOvernutritionGlucose Metabolism DisordersOverweight

Criteria

5 inclusion criteria required to participate
healthy adult men and women 18-45 years of age

BMI 18-40 kg/m2

not pregnant, premenopausal with regular menstrual cycles

not breastfeeding

Show More Criteria

4 exclusion criteria prevent from participating
medications known to affect sleep, autonomic control, blood lactate levels or metabolic, or cardiovascular function (PI discretion)

self-reported history of hepatic, renal, pulmonary, cardiovascular, or neurological disease, stroke or neurovascular disease, bleeding/clotting disorders, sleep apnea or other sleep disorders, diabetes, history of alcoholism or substance abuse

major cardiovascular event or surgical procedure within the past three months

hypertension (>140/90 mmHg or at PIs discretion).

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

University of Missouri

Columbia, United StatesOpen University of Missouri in Google Maps
Recruiting
One Study Center
Cerebral Lactate Uptake in Obese and Non-Obese Individuals | PatLynk