Actively Recruiting
Intermittent Cold Exposure and Brown Adipose Tissue Hyperplasia
Led by University of Edinburgh · Updated on 2025-07-09
12
Participants Needed
1
Research Sites
60 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This clinical trial explores how repeated short-term cold exposure impacts the molecular and physiological function of brown adipose tissue (BAT), a thermogenic organ associated with improved cardiometabolic health. While intermittent cold exposure has been shown to increase BAT activity and mass, as measured by fluorodeoxyglucose (18F-FDG) uptake on positron emission tomography/computed tomography (PET/CT) scans, the molecular adaptations within BAT and other thermogenic tissues including skeletal muscle and white adipose tissue (WAT) remain poorly understood. Healthy adults aged 18 to 40 years (6 males and 6 females) will participate in a 10-day cold acclimation protocol (2 hours per day using water-perfused cooling blankets). The primary objective is to determine how cold exposure alters cellular heterogeneity and gene expression in BAT, WAT, and skeletal muscle. Participants will undergo baseline assessments, including measurements of energy expenditure, core and skin temperature, muscle activity, and blood sampling, each performed in both warm and cold conditions. These assessments will be followed by dynamic total-body PET/CT imaging during cold exposure and tissue biopsies from BAT, subcutaneous WAT, and skeletal muscle. These procedures will be repeated after the cold acclimation protocol to evaluate physiological and molecular changes. Additional outcomes include changes in energy expenditure, cold tolerance, and immune cell responses induced by cold exposure.
CONDITIONS
Official Title
Intermittent Cold Exposure and Brown Adipose Tissue Hyperplasia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18-40 years
- Body mass index 18.5-25 kg/m2
- Weight change of less than 5% in the past 6 months
- No acute or chronic medical conditions
- Not taking regular medications except contraceptives for females
- No claustrophobia
- Alcohol intake of 14 units or less per week
- Screening blood tests within acceptable limits
- Not currently pregnant, lactating, or breastfeeding (for females)
- Ability to give informed consent
You will not qualify if you...
- Not meeting the inclusion criteria
- Contraindication to PET/CT scan
- Allergy to local anesthetic
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Royal Infirmary of Edinburgh
Edinburgh, United Kingdom
Actively Recruiting
Research Team
M
María Paula Huertas Caycedo
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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