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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
ClinicalTrials.gov ID: NCT07423988
What this study is testing
- What it's testing
- 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.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 65. Healthy volunteers may be eligible.
You may be able to join if
- Group "with on-call night at high altitude at the Pic du Midi":
- Employed at the Pic du Midi for at least one month
- Working nights at high altitude (at the Pic du Midi, altitude of 2877m) as part of their professional activity
- Person affiliated with or covered by a social security scheme
- Free, informed, and written consent signed by the participant and the investigator Night group "without on-call night at high altitude":
You likely can't join if
- For all participants:
- History of cardiovascular disease
- Use of cardiovascular/psychotropic medication
- Participant under legal guardianship or other protective regime (guardianship, curatorship)
- Pregnant or breastfeeding woman
- French language proficiency insufficient to complete the questionnaires
See the full eligibility criteria
- Group "with on-call night at high altitude at the Pic du Midi":
- Employed at the Pic du Midi for at least one month
- Working nights at high altitude (at the Pic du Midi, altitude of 2877m) as part of their professional activity
- Person affiliated with or covered by a social security scheme
- Free, informed, and written consent signed by the participant and the investigator Night group "without on-call night at high altitude":
- Employed at the Pic du Midi for at least one month
- Not working nights at high altitude (at the Pic du Midi, altitude of 2877m) as part of their professional activity
- Person affiliated with or covered by a social security scheme social
- Free, informed and written consent signed by the participant and the investigator
- For all participants:
- History of cardiovascular disease
- Use of cardiovascular/psychotropic medication
- Participant under legal guardianship or other protective regime (guardianship, curatorship)
- Pregnant or breastfeeding woman
- French language proficiency insufficient to complete the questionnaires
The study team makes the final eligibility decision.
Where it's taking place
- Toulouse, Oui, France
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 65 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Toulouse, Oui, France. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.