Descriptive Study of the PSYchological Impact of CONFinement Measures in

Status Recruiting

Clinical Trial Summary

Quarantine is an unpleasant experience : separation from loved ones, loss of freedom, uncertainty about infection status, boredom. It may lead to negative mental health consequences and thus the emergence of anxiety and depressive symptoms. From March 17th, 2020 to May 11th 2002, the French government has implemented national containment measures due to the Covid-19 epidemic. Although there are data on the psychological impact and experience of quarantine measures in people who have been infected or suspected of being carriers of certain pathogens (e.g. Ebola), there are no data on such impact in the French population and quarantines lasting longer than 21 days. Investigators therefore propose to conduct a human and social sciences study in order to better understand the current situation

Clinical Trial Description

The main objective is to describe the psychological state during confinement (and the impact of the confinement) in a sample of the French general population. Secondary objectives : - to assess the evolution of psychological health between the period of confinement and post-confinement. - to identify clinical factors modulating psychological state during confinement It is expected to highlight : - a link between the intensity of anxiety symptoms and the number/quality of social contacts - a reduction of anxiety and depression symptoms in the post-confinement period. - higher consumption of drugs during the confinement period Self-questionnaires (Google form format) are sent by mailing lists or social networks to participants in order to complete the assessment of psychological state. A unique identifier is sent in a separate email. These assessments are performed at least once during the confinement period. It is planned to repeat them when the confinement is lifted: 15 days, 3 and 6 months after the lifting of the confinement because of the risk of developing anxiodepressive symptoms, in particular post-traumatic stressors. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04374643
Study type	Observational
Source	University Hospital, Montpellier
Contact	Emilie Olie, MD PhD
Phone	+33 4 67 33 85 81
Email	e-olie@chu-montpellier.fr
Status	Recruiting
Phase
Start date	April 1, 2020
Completion date	December 30, 2021

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Descriptive Study of the PSYchological Impact of CONFinement Measures in the General Population — PsyConfPop

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms