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NCT04308187 Clinical Trial

Influence of the COvid-19 Epidemic on STRESS

Stress, Psychological Clinical Trial

— COVISTRESS  

Official title:
The COVISTRESS Study: Influence of the COvid-19 Epidemic on STRESS

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04308187
Other study ID # 2020 COVISTRESS
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 11, 2020
Est. completion date March 2022

Study information
Verified date March 2020
Source University Hospital, Clermont-Ferrand
Contact Lise Laclautre
Phone 0473754963
Email promo_interne_drci@chu-clermontferrand.fr
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The Coronavirus has a major influence on stress for the general population. However, data are currently non-existent concerning the perception and knowledge of the epidemic, the feeling of information from companies / establishments / governments, the means of protection used, the feelings of fear generated and their impact on feelings of stigmatization towards certain ethnic groups or categories of patients (those who cough ...), or relationships with socio-demographic factors or lifestyle.

Description:

This is an observational study using a REDCap® questionnaire via an internet link, which will be distributed by any means (Facebook, Twitter, institution mailing lists via a referent, flash codes distributed to patients and the public, etc.).

The self-questionnaire will assess stress, perception and knowledge of the epidemic, the feeling of information on the part of businesses / establishments / governments, the means of protection used the feelings of fear generated and their impact on feelings of stigmatization towards certain ethnic groups or categories of patients (those who cough ...), or relationships with socio-demographic factors or lifestyle.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 50000
Est. completion date March 2022
Est. primary completion date March 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Anyone volunteer to participate

Exclusion Criteria:

- Anyone non-voluntary to participate

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France University Hospital, Clermont-Ferrand Clermont-Ferrand

Sponsors (4)
Lead Sponsor Collaborator
University Hospital, Clermont-Ferrand Faculty of Medicine, Clermont-Ferrand, France, UMR CNRS 6024 LaPSCo, Clermont-Ferrand, France, Wittyfit, Paris, France

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Stress Stress level will be assessed by questionnaire Day 1
Secondary Perception and knowledge of the epidemic Perception and knowledge of the epidemic will be assessed by questionnaire Day 1
Secondary Feeling of information on the part of companies / establishments / governments The feeling of information will be assessed by questionnaire Day 1
Secondary Means of protection the means of protection used will be assessed by questionnaire Day 1
Secondary Feelings of fear generated and its impact on feelings of stigmatization towards ethnic groups or categories of patients The feeling of fear and the impact on stigmatization 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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