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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04567017
Other study ID # PO19103
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date October 1, 2020
Est. completion date October 1, 2021

Study information

Verified date September 2019
Source CHU de Reims
Contact Vincent LEGROS
Phone 03 26 78 30 21
Email vlegros@chu-reims.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


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


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date October 1, 2021
Est. primary completion date October 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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 Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Damien JOLLY Reims

Sponsors (1)

Lead Sponsor Collaborator
CHU de Reims

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary measurement of physical activity in physician according to seniority mean distance in meter according to seniority Day 1
Secondary measurement of physical activity in physician mean distance in meter Day 1
Secondary measurement of attention function score in Birckenkamp D2-R test Day 1
Secondary sleep duration average sleep time Day 1
Secondary quality of sleep mean score on Spiegel scale Day 1