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Evaluation of Changes in Sleep Efficiency Among PIC DU MIDI Employees Between Nights Spent at Home and Nights Spent in a High Altitude Work Environment
Led by University Hospital, Toulouse · Updated on 2026-04-08
32
Participants Needed
1
Research Sites
3 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate changes in sleep efficiency and cardiorespiratory parameters among employees who work under high-altitude conditions at the Pic du Midi. The study focuses on understanding sleep disruptions caused by acute exposure to high altitude, especially in employees who experience cyclical hypoxic stress. It seeks to clarify sleep quality indicators which are rarely measured in such extreme environments. The study compares two groups of employees: those who spend the night at high altitude (2877 meters) while on call at the Pic du Midi summit, and those who work during the day but sleep at home at lower altitude. Sleep recordings using polysomnography and questionnaires are used to monitor and compare nights spent at home versus nights spent at high altitude. This includes a one-week observation period following participant inclusion. Participants will undergo sleep efficiency monitoring, measuring total sleep time compared to total sleep period, alongside evaluation of various sleep and cardiac parameters. Questionnaires help assess sleep disorders and their correlation with sleep quality. The study monitors participants for one week after inclusion and compares sleep data across groups to better understand the impact of high-altitude work on sleep patterns and related health parameters.
CONDITIONS
Brief Title
Evaluation of Changes in Sleep Efficiency Among PIC DU MIDI Staff Between Nights Spent at Home and Nights Spent in the Workplace Under High Altitude Conditions
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Employed at the Pic du Midi for at least one month
- Working nights at high altitude (2877 meters) as part of job, or not working nights at high altitude (separate groups)
- Affiliated with or covered by a social security scheme
- Able to provide free, informed, written consent
You will not qualify if you...
- History of cardiovascular disease
- Use of cardiovascular or psychotropic medication
- Under legal guardianship or other protective regime
- Pregnant or breastfeeding women
- Insufficient French language skills to complete questionnaires
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 - 1 week after inclusion
Participants undergo polysomnography and complete questionnaires to measure sleep efficiency and other sleep parameters under different altitude conditions.
Overnight sleep recordings at home and at high altitude depending on group assignment
Trial Site Locations
Total: 1 location
1
Unité du sommeil, Hôpital Pierre Paul Riquet, 1 place du Docteur Baylac
Toulouse, Oui, France, 31059
Actively Recruiting
Research Team
R
Rachel DEBS, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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