Effects of a Sleep Education Program on the Health Status of Healthcare Workers Working 12-hour Alternating Day-night Shifts
NCT ID: NCT07326579
Last Updated: 2026-01-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
160 participants
INTERVENTIONAL
2026-06-01
2030-06-01
Brief Summary
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Therefore, this study aims to investigate the effects of a 6-month sleep education program conducted by occupational health nursing staff, on the sleep duration of healthcare workers newly exposed to alternating 12-hour day and night shifts.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Sleep educational
Personalized educational program
Sleep educational
Participants will undergo :
* standardized monitoring initially (M0), then at 6 months (M6) and 12 months (M12)
* a personalized educational program, including an initial consultation with a sleep doctor and a nurse, followed by monthly follow-ups with an occupational health nurse.
Control
Standard workplace medicine advice
No interventions assigned to this group
Interventions
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Sleep educational
Participants will undergo :
* standardized monitoring initially (M0), then at 6 months (M6) and 12 months (M12)
* a personalized educational program, including an initial consultation with a sleep doctor and a nurse, followed by monthly follow-ups with an occupational health nurse.
Eligibility Criteria
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Inclusion Criteria
* Working 12-hour shifts (day/night)
* Working at least 80% of a full-time equivalent post
* Staff employed at a hospital listed among the investigating centers
* Being affiliated or entitled under a social security scheme
* Having received informed information about the study and have co- signed, with the investigator, a consent to participate in the study
Exclusion Criteria
* Nursing staff and nursing assistants with a history of mental illness or who are taking medication that affects alertness (psychotropic drugs)
* Pregnant or breastfeeding women
* Nursing staff or nursing assistants with sleep apnea syndrome, central hypersomnolence disorders, severe parasomnias, severe untreated restless legs syndrome
* Individuals with children under the age of 1 in the household
* Trans meridian travel (\>2 time zones) during the month prior to the study
18 Years
65 Years
ALL
Yes
Sponsors
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Centre Hospitalier Universitaire de Saint Etienne
OTHER
Responsible Party
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Locations
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Chu Grenoble
Grenoble, , France
Hospices Civils de Lyon
Lyon, , France
Chu Saint-Etienne
Saint-Etienne, , France
Countries
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Facility Contacts
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Other Identifiers
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2025-A02584-45
Identifier Type: OTHER
Identifier Source: secondary_id
25PH236
Identifier Type: -
Identifier Source: org_study_id
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