Actively Recruiting
Monitoring of Job Stress Related to Night Shifts in Ophthalmology Physicians and Residents
Led by University Hospital, Clermont-Ferrand · Updated on 2025-03-14
30
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University Hospital, Clermont-Ferrand
Lead Sponsor
U
University Clermont Auvergne (UCA), Clermont-Ferrand, France
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to study how prolonged working hours, up to 60 consecutive hours, affect stress and heart rate variability (HRV) in ophthalmology physicians and residents. These healthcare professionals often face stressful night emergency shifts combined with regular daytime work, leading to fatigue, mental exhaustion, and potential impacts on work quality and health. The study focuses on how these demanding conditions influence physiological stress markers and cognitive performance. Participants wear a heart rate belt and a watch that measure physical activity and skin conductance continuously for 34 hours. They also wear an EEG monitor during sleep to assess sleep quality. The study includes five different conditions: a control day with no work, a typical working day, a working day plus one night shift, an emergency working day with two consecutive night shifts, and a night shift alone. After the monitoring period, participants perform a cataract surgery simulator test and provide saliva samples for biomarker analysis. Questionnaires on quality of life and stress-related factors are completed at the start and end of each session. During the study, researchers collect data on heart rate variability, stress levels, fatigue, burnout, depression, anxiety, and sleep quality at the beginning and end of the 34-hour monitoring period. They also measure saliva biomarkers related to stress and evaluate physical activity and sedentary behavior. Surgical performance on the simulator is assessed at the end. The study lasts for up to five participation sessions per individual, allowing detailed evaluation of the effects of prolonged work on stress and performance.
CONDITIONS
Brief Title
JOB STRESS in OPHthalmology Physicians and Residents
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Ophthalmologists who have completed the ophthalmology specialized studies diploma, and ophthalmology residents working in the ophthalmology department of the university hospital center of Clermont-Ferrand
- Ability to provide written informed consent to participate
- Affiliation with a social security system
- Age between 18 and 65 years old
You will not qualify if you...
- Refusal to participate in the study
- Children under 18 years old
- Pregnant or breastfeeding women
- Adults under legal guardianship
- Adults deprived of their liberty
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit
Duration - 34 hours per session, up to 5 sessions
Participants are monitored for 34 hours wearing a heart rate belt and a watch measuring physical activity and skin conductance. An EEG monitor is worn during sleep to assess sleep quality. Saliva tests and quality of life questionnaires are completed at the start and end of the monitoring period. A surgical simulator test is performed at the end of each monitoring session.
Up to 5 monitoring sessions lasting 34 hours each
Trial Site Locations
Total: 1 location
1
CHU clermont-ferrand
Clermont-Ferrand, France
Actively Recruiting
Research Team
L
Lise Laclautre
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SCREENING
Number of Arms
1
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