- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04567017
Physical Activity of Staff on Medical Duty in a Department of Anesthesia and Critical Care During Guards (AMAC)
On-call work is an integral part of senior and junior patricians in a critical care department.
Several studies have examined the effect of sleep deprivation on physicians on call and the impact of sleep deprivation on the quality of patient care.
Some of these studies have shown that practitioners' concentration capacities have deteriorated as the guard progresses.
However, few studies have looked at the physical activity of practitioners over a period of on-call time (distance covered, number of steps,...), as well as other parameters than the time spent in communication over the telephone.
The age and seniority of practitioners seem to be factors that can influence these different parameters, and there are few figures in the literature.
Study Overview
Status
Conditions
Detailed Description
Practitioners and juniors will be informed of the study. If they agree to participate in the study, each volunteer will receive an assessment of their cognitive functions before taking up their duties via the Montréal Cognitive Assessment (MOCA) version 7.1.
The place of exercise (emergencies, anaesthesia and ICU Each participant will be equipped with a connected watch with pedometer and cardiofrequencemeter function (Fitness Tracker F07Max).
During his on-call period a questionnaire will be given to him, with socio-demographic data, sleep duration and quality and the number of acts during the on-call period.
The telephone data will be analysed by querying the internal telephone system of the Reims University Hospital.
At the end of the on-call period, the analysis of the data from the connected watch will be analyzed and each volunteer will benefit from an evaluation of his cognitive functions via the Montreal Cognitive Assessment (MOCA) version 7.3 after taking up his duties.
Data will be collected during 2 shifts for each practitioner and junior
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Vincent LEGROS
- Phone Number: 03 26 78 30 21
- Email: vlegros@chu-reims.fr
Study Locations
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-
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Reims, France
- Damien JOLLY
-
Contact:
- Vincent LEGROS
- Phone Number: 03 26 78 30 21
- Email: vlegros@chu-reims.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
inclusion criteria :
- voluntary practitioners and residents of the critical care department (intensive care, emergencies and anaesthesia)
exclusion criteria :
- refusal to participate
- musculoskeletal disorders
- a significant medical history that prevents normal physical activity for age
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
measurement of physical activity in physician according to seniority
Time Frame: Day 1
|
mean distance in meter according to seniority
|
Day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
measurement of physical activity in physician
Time Frame: Day 1
|
mean distance in meter
|
Day 1
|
measurement of attention function
Time Frame: Day 1
|
score in Birckenkamp D2-R test
|
Day 1
|
sleep duration
Time Frame: Day 1
|
average sleep time
|
Day 1
|
quality of sleep
Time Frame: Day 1
|
mean score on Spiegel scale
|
Day 1
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- PO19103
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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