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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04436861
Other study ID # Decovid
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date June 28, 2020
Est. completion date July 1, 2020

Study information

Verified date April 2022
Source Clinique Medipole Garonne
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigator wish to study, at a distance from the lifting of confinement (1 month), whether the psychological impact on professionals in nursing and non-nursing care establishments is associated with their living context (professional and personal situation) during confinement.


Description:

The context of confinement and of the global pandemic is a major source of stress for the entire population: separation of loved ones, loss of freedom, uncertainty about the infectious status, boredom. All of these factors can cause negative mental health consequences. Having little social contact was one of the factors increasing the negative psychological impact of confinement. People suffering from psychological disorders are particularly vulnerable during quarantine periods. On March 17, 2020, the French government implemented national containment measures due to the Covid-19 epidemic. Although the effects of containment have been studied for fragile populations, no study to date has focused on the specific population of healthcare facility staff. These caregivers have for the most part continued their professional activity, but they have been confronted with the fear of contracting or causing patients to contract Covid-19. At a distance from the lifting of confinement (1 month), the investigator wish to study whether the highlighting of anxiety or depression in these healthcare professionals is associated with their context of life (professional and personal situation) during confinement


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 1, 2020
Est. primary completion date June 28, 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Nursing and non-nursing care professionals Exclusion Criteria: - Refusal to participate - Subject included in an interventional study

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Clinique Medipole Garonne

Outcome

Type Measure Description Time frame Safety issue
Primary Demonstration of the level of anxiety / depression of healthcare professionals and non-healthcare professionals one month after the confinement period Anxiety-depression will be assessed by the hospital anxiety and depression scalequestionnaire. The context of life during confinement will be assessed by a self-questionnaire collecting data relating to lifestyle and work. 1 month
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