Actively Recruiting
Appetite and Energy Intake in Young Female Adults During and After Simulated High-Altitude
Led by University of Ottawa · Updated on 2025-04-04
10
Participants Needed
1
Research Sites
N/A
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
This research aims to study the effects of acute passive continuous hypoxemia, or simulated high-altitude exposure, on appetite and energy intake in healthy young female adults aged 18 to 30. The study seeks to understand whether six hours at a simulated altitude of 5000 meters reduces subjective appetite scores and energy intake, and if these changes last after the exposure ends. Researchers will compare these effects with a control condition at normal sea-level oxygen levels to see if low oxygen alone impacts appetite and intake. Participants will take part in two randomized, single-blind experimental sessions. Each session involves six hours of passive exposure to either normal oxygen (normoxia) or simulated high-altitude conditions (hypoxia) in a climate-controlled chamber set at 22°C with 30% humidity. During exposure, participants remain fasted. After leaving the chamber, they will be offered foods from a selected list in unlimited amounts to assess energy intake following the exposure. Participants will visit the laboratory for a preliminary screening to confirm eligibility. During and after exposures, researchers will measure changes in appetite feelings such as desire to eat, hunger, fullness, and prospective food consumption at baseline, 6 hours, and 24 hours. Energy intake will be tracked immediately post-exposure and later. Additional assessments include heart rate, oxygen saturation, blood pressure, acute mountain sickness symptoms, fluid balance, sensory changes, metabolic rates, and blood markers. The total study duration includes both exposure sessions and follow-up assessments.
CONDITIONS
Brief Title
Hypoxia, Appetite, and Energy Intake in Young Female Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- English or French speaking
- Ability to provide informed consent
- Female aged 18 to 30 years
- Healthy with no chronic diseases
- Not pregnant, not in puerperium, and regular menstrual cycles
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
- Ongoing smoking status
- Experiencing pregnancy, puerperium, or irregular menstrual cycles
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Two 6-hour exposure periods with washout between sessions
Participants undergo two separate 6-hour passive exposures in a climate-controlled environmental chamber: one under normoxia and one under simulated high-altitude hypoxia at 5000 meters. Participants remain fasting during each exposure. Appetite, energy intake, and various physiological measures are assessed before, during, and after each exposure.
2 visits (one for each exposure condition)
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
Research Team
P
Pascal Imbeault, PhD
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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