Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
Healthy Volunteers
ID05822141

Omega-3 Fatty Acid Modulation of Brown Adipose Tissue for Arctic Resilience

Led by Indiana University · Updated on 2026-05-26

30

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how fish oil supplements might affect how the body regulates temperature, especially through brown fat activation, shivering, skin blood flow, and comfort during cold exposure. This study focuses on healthy adults aged 18 to 40 years and uses a controlled environment to see how these supplements influence responses to cold. The trial is randomized, double-blind, and placebo-controlled to ensure reliable results. Participants will be randomly assigned to one of two groups: one group will take six capsules of fish oil daily, providing 7.8 grams of omega-3 fatty acids (including EPA and DHA), while the other group will take six capsules of olive oil as a placebo. This treatment lasts for 12 weeks. Before supplementation and at 6 and 12 weeks after starting, participants will undergo cold exposure tests in an environmental chamber where the air temperature gradually decreases from 29°C to 4°C over 125 minutes. During the study visits, researchers will measure core body temperature, metabolic heat production, brown fat activation through infrared thermography, shivering using accelerometry and electromyography, skin blood flow, and thermal comfort. Tests like the Minnesota Manual Dexterity Test and the Nine Hole Peg Test will assess motor function. Additional measurements include blood pressure, heart and pulse rates, body composition, and dietary recalls over the 12-week period. The study aims to gain detailed insight into how fish oil affects cold tolerance and thermoregulation.

CONDITIONS

Brief Title

Omega-3 Fatty Acids as Regulators of Brown Adipose Tissue During Cold Exposure

Who Can Participate

Age: 18Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male and female, between the ages of 18 to 40 years
  • Body Mass Index (BMI) of 18.5 to 24.9 kg/m2
  • Considered moderately to highly active by the International Physical Activity Questionnaire (IPAQ) and the Physical Activity Readiness Questionnaire (PAR-Q+)
Not Eligible

You will not qualify if you...

  • History of smoking or recreational smoking
  • History of hyperlipidemia, hypertension, cardiovascular disease, diabetes, renal disease, neurological disease, metabolic disease, bleeding disorders, or delayed clotting time
  • Taking SSRIs, ADD/ADHD medication, or chronic pain medication
  • Chronic or acute rectal disorders such as cancer, surgery, hemorrhoids, diarrhea, or constipation
  • Diagnosis of immune suppression or autoimmune diseases
  • Pregnant or planning to become pregnant
  • Resting blood pressure over 130 mmHg systolic or 90 mmHg diastolic
  • Resting pulse rate over 100 beats per minute
  • Regularly consuming fish oil supplements or eating more than one fish meal per week
  • Consuming more than one fish meal per week during the study

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 12 weeks

Participants take either fish oil or placebo capsules daily for 12 weeks to study the effects on brown adipose tissue and body temperature regulation during cold exposure.

Baseline visit and 2 follow-up visits at 6 and 12 weeks

Trial Site Locations

Total: 1 location

1

Human Perfromance Lab, Indiana University

Bloomington, Indiana, United States, 47405

Actively Recruiting

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Research Team

T

Timothy D Mickleborough, PhD

A

Abigail S Sogard, B.S.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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