Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
Healthy Volunteers
NCT07048405

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

Age: 18Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • Not meeting the inclusion criteria
  • Contraindication to PET/CT scan
  • Allergy to local anesthetic

AI-Screening

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Trial Site Locations

Total: 1 location

1

Royal Infirmary of Edinburgh

Edinburgh, United Kingdom

Actively Recruiting

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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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