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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

Evaluation of Changes in Sleep Efficiency Among PIC DU MIDI Employees Between Nights Spent at Home (Without Increased Altitude) and Nights Spent in a Professional Environment Under High Altitude Conditions

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07423988
Acronym
ALTISOM
Enrollment
32
Registered
2026-02-20
Start date
2026-02-01
Completion date
2027-02-28
Last updated
2026-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep Disorder (Disorder)

Keywords

sleep, high altitude, sleep disorder, cardiorespiratory parameters

Brief summary

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..

Interventions

Polysomnography and questionnaires.

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion 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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Comparison of sleep efficiency (total sleep time / total sleep period) under high altitude conditions (at 2877 m) versus without increased altitude (at home)1 week after the inclusionSleep efficiency will be compared, according to the ratio = total sleep time (TST)/ total sleep period (PTS) calculated from a polysomnographic recording, between the night spent at high altitude (2877m, at PIC du MIDI) and the second night spent at home (not increased altitude) among PIC du MIDI employees performing on-call nights at high altitude.

Secondary

MeasureTime frameDescription
Comparison of sleep parameters in high altitude conditions versus without increased altitude for the group "with on-call night at high altitude at Pic du Midi"1 week after the inclusionSleep parameters (determined according to the criteria of the American Academy of Sleep Medicine (AASM)) measured from a polysomnographic recording will be compared in high altitude conditions versus without increased altitude.
Measurement of sleep parameters in low altitude conditions for the group "without on-call nights at high altitude"1 week after the inclusionSleep parameters (determined according to the criteria of the American Academy of Sleep Medicine (AASM)) will be measured from a polysomnographic recording under conditions without altitude gain.
Evaluation of the relationship between sleep quantification criteria and sleep disorder criteria1 week after the inclusionComparison of questionnaire responses and polysomnographic recording
Correlation between cardiac parameters and sleep efficiency.1 week after the inclusionCorrelation between heart rate variability and sleep efficiency using polysomnography recording
Comparison of sleep parameters, in conditions without increased altitude, between the 2 groups of participants1 week after the inclusionComparison of sleep parameters (determined according to the criteria of the American Academy of Sleep Medicine (AASM)) from the polysomnography recording between the two groups in conditions without increased altitude

Countries

France

Contacts

CONTACTRachel DEBS, MD
debs.r@chu-toulouse.fr05 61 77 94 88

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026