Influence of the COvid-19 Epidemic on STRESS
COVISTRESS
The COVISTRESS Study: Influence of the COvid-19 Epidemic on STRESS
1 other identifier
observational
50,000
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2020
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 11, 2020
CompletedFirst Submitted
Initial submission to the registry
March 12, 2020
CompletedFirst Posted
Study publicly available on registry
March 13, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2022
CompletedMarch 13, 2020
March 1, 2020
2 years
March 12, 2020
March 12, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Stress
Stress level will be assessed by questionnaire
Day 1
Secondary Outcomes (5)
Perception and knowledge of the epidemic
Day 1
Feeling of information on the part of companies / establishments / governments
Day 1
Means of protection
Day 1
Feelings of fear generated and its impact on feelings of stigmatization towards ethnic groups or categories of patients
Day 1
Sociodemographic factors and lifestyle habits
Day 1
Eligibility Criteria
General population
You may qualify if:
- Anyone volunteer to participate
You may not qualify if:
- Anyone non-voluntary to participate
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University Hospital, Clermont-Ferrandlead
- UMR CNRS 6024 LaPSCo, Clermont-Ferrand, Francecollaborator
- Wittyfit, Paris, Francecollaborator
Study Sites (1)
University Hospital, Clermont-Ferrand
Clermont-Ferrand, 63000, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Fréderic DUTHEIL
University Hospital, Clermont-Ferrand
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 1 Day
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 12, 2020
First Posted
March 13, 2020
Study Start
March 11, 2020
Primary Completion
March 1, 2022
Study Completion
March 1, 2022
Last Updated
March 13, 2020
Record last verified: 2020-03