Actively Recruiting

Phase Not Applicable
Age: 18Years - 30Years
FEMALE
Healthy Volunteers
NCT06912230

Hypoxia, Appetite, and Energy Intake in Young Female Adults

Led by University of Ottawa · Updated on 2025-04-04

10

Participants Needed

1

Research Sites

54 weeks

Total Duration

On this page

Sponsors

U

University of Ottawa

Lead Sponsor

N

Natural Sciences and Engineering Research Council, Canada

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to investigate the effects of acute passive continuous hypoxemia (simulated high-altitude at rest) on appetite and energy intake in healthy young female adults. The main questions it aims to answer are: * Does six hours of simulated high-altitude (5000 meters) reduce scores of subjective appetite and energy intake? * Do changes in appetite and energy intake persist in the hours following the end of hypoxic exposure? Researchers will compare the effects of simulated high-altitude to a control normoxia (sea-level) condition to see if exposure to low oxygen levels independently affect appetite and energy intake. Participants will: * Visit the laboratory for a preliminary screening session to assess eligibility. * Undergo two randomized, single-blind, experimental sessions consisting of six hours of passive exposure to normoxia or hypoxia in a climate-controlled chamber. * Consume foods provided from a curated list, served in ad libitum quantities, after leaving the laboratory to assess post-exposure energy intake.

CONDITIONS

Official Title

Hypoxia, Appetite, and Energy Intake in Young Female Adults

Who Can Participate

Age: 18Years - 30Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Speak English or French
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • History or evidence of chronic disease
  • Current use of hypolipemic medication
  • Current use of hormonal contraceptives
  • Current use of antidepressants
  • Current use of anticoagulants
  • Currently smoking
  • Pregnant, recently gave birth, or have irregular menstrual cycles

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Behavioural and Metabolic Research Unit, School of Human Kinetics, Faculty of Health Sciences, University of Ottawa

Ottawa, Ontario, Canada, K1N 6N5

Actively Recruiting

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Research Team

P

Pascal Imbeault, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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