Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
ID07423988

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

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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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)

Sleep Recording

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

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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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