- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04538586
Influence of the COVId-19 Pandemic on STRESS, and Screening Procedures (COVISTRESS Screening)
September 3, 2020 updated by: University Hospital, Clermont-Ferrand
Influence of the COVId-19 Pandemic on STRESS, and Screening Procedures
Coronavirus has caused containment of more than a third of the world's population.
Some countries have used a major screening strategy.
Screening procedures, such as waiting (or resulting) for the test, can be stressful and can attract the most stressed people.
However, there is currently no data on the relationship between stress and screening for SARS-CoV2
Study Overview
Status
Recruiting
Conditions
Detailed Description
This is an observational study by REDCap questionnaire® via a flyer deposited in the waiting room of the COVID screening centres.
No incentive to complete the questionnaire will be made.
The self-survey will assess stress and its relationship to SARS-CoV2 screening procedures, socio-demographic factors or lifestyle habits.
This Screening questionnaire includes 31 questions.
Study Type
Observational
Enrollment (Anticipated)
1000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Clermont-Ferrand, France, 63000
- Recruiting
- Univeristy Hospital, Clermont-Ferrand
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years and older (ADULT, OLDER_ADULT, CHILD)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
People screened for COVID-19
Description
Inclusion Criteria:
- All volunteers who are screened
Exclusion Criteria:
- None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stress measures
Time Frame: Day 1
|
Attitudes and stress related to screening procedure will be measured via questionnaire
|
Day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Screening
Time Frame: Day 1
|
Attitudes towards screening will be measured via questionnaire
|
Day 1
|
|
Sociodemographic characteristics
Time Frame: Day 1
|
Age, gender, qualification, personal work status, ethnicity, life characteristics and stress will be assessed by questionnaires
|
Day 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
May 1, 2020
Primary Completion (ANTICIPATED)
December 1, 2020
Study Completion (ANTICIPATED)
December 1, 2025
Study Registration Dates
First Submitted
September 3, 2020
First Submitted That Met QC Criteria
September 3, 2020
First Posted (ACTUAL)
September 4, 2020
Study Record Updates
Last Update Posted (ACTUAL)
September 4, 2020
Last Update Submitted That Met QC Criteria
September 3, 2020
Last Verified
September 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020 COVISTRESS Screening
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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