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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04954105
Other study ID # 2020 COVISTRESS HRV
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 15, 2020
Est. completion date January 2022

Study information

Verified date July 2021
Source University Hospital, Clermont-Ferrand
Contact Lise Laclautre
Phone 334.73.754.963
Email promo_interne_drci@chu-clermontferrand.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The COVID-19 pandemic is an exceptional and particularly anxiety-provoking health situation. In particular, for healthcare professionals who come into contact with patients who are contaminated or suspected of contamination, such as emergency rooms. The management of these patients requires reinforced protective equipment. However, in the context of this pandemic, data is currently non-existent on the objective measurement of the stress of these professionals. Sinus variability of heart rate is a biomarker of stress measured with a simple heart rate monitor or a watch, completely painless, non-intrusive, and used by the general public routinely in many areas (monitoring sports sessions, etc.).


Description:

This is an observational study. In the emergency room, each participant will wear a heart rate monitor and a consumer watch throughout the working day (there will be no measurement on duty at night, nor measurement at home). The days will be notified as being in the "COVID sector", "non-COVID sector" or "Trauma Room". Each participant will complete a questionnaire comprising visual analog scales on the feeling (health concern, stress, fatigue, quality of sleep, anxiety, morale, burnout, decisional latitude, psychological demand, support, self-esteem), time of start and end of work, and socio-demographic data (sex, age, weight, height, smoking)


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date January 2022
Est. primary completion date January 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Emergency health care worker Exclusion Criteria: - refusal to participate

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France CHU clermont-ferrand Clermont-Ferrand

Sponsors (4)

Lead Sponsor Collaborator
University Hospital, Clermont-Ferrand UMR CNRS 6024 LaPSCo, Clermont-Ferrand, France, University Hospital of Clermont-Ferrand (CHU), Clermont-Ferrand, France, Wittyfit, Paris, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Heart-Rate Variability (HRV) HRV is a measure of the variation in time between each heartbeat. This variation is controlled by the autonomic nervous system. It works regardless of our desire and regulates, among other things, our heart rate, blood pressure, breathing, and digestion. It will be assess by heart rate monitor up to day 1
Secondary Stress Stress level will be assessed by questionnaire hours 0 at day 1
Secondary Stress Stress level will be assessed by questionnaire hours 24 at day 1
Secondary Perception of the epidemic Perception of the epidemic will be assessed by questionnaire day 1
Secondary Sociodemographic factors and lifestyle habits Sociodemographic factors and lifestyle habits will be assessed by questionnaire day 1
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