Actively Recruiting
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
Led by University Hospital, Toulouse · Updated on 2026-04-08
32
Participants Needed
1
Research Sites
48 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Sleep organization and cardiorespiratory parameters are disrupted in extreme conditions such as high altitude. The pathophysiology of medical problems related to acute high-altitude exposure is partially understood, but sleep quality indicators are very rarely measured under these conditions. This lack of information is even more pronounced among employees subjected to cyclical exposure to high-altitude hypoxic stress, as is the case for the employees at the Pic du Midi. These 32 employees regularly report to their occupational physician difficulties in managing their sleep disorders, struggling to distinguish symptoms from objective changes in their sleep cycles. Among them, 13 are on call at the summit of the Pic du Midi (2,877 m), while 19 work there during the day and return home to a lower altitude at night to sleep. The investigators also wish to measure structural changes in sleep and its cardiorespiratory parameters using polysomnography in these 13 employees, comparing nights spent at home at normal altitude with those spent at the summit of the Pic du Midi. These changes will also be compared to those of a group of 19 employees who do not sleep at high altitude..
CONDITIONS
Official 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 (2877m) as part of professional activity (for the night group)
- Not working nights at high altitude (2877m) as part of professional activity (for the day group)
- Affiliated with or covered by a social security scheme
- Free, informed, and written consent signed by participant and investigator
You will not qualify if you...
- History of cardiovascular disease
- Use of cardiovascular or psychotropic medication
- Participant under legal guardianship or protective regime
- Pregnant or breastfeeding woman
- Insufficient proficiency in French to complete questionnaires
AI-Screening
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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
CONTACT
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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