Identifying Functional and Psycho-social Complaints After Hospitalization for SARS-CoV-2 Infection( COVID 19)- REPERCOV

Centre Hospitalier le Mans

Status: Unknown

Conditions: SARS-COV2; COVID19

Treatments: Other: questionnaire

Study type: Interventional

Funder types: Other

Identifiers

NCT04561154

CHM-2020/S10/04

Details and patient eligibility

About

Since December 2019, China and then the rest of the world have been affected by the rapid spread of a new coronavirus infection called SARS-CoV-2 (severe acute respiratory syndrome coronavirus), the clinical expression of which is called Covid-19 (Coronavirus Disease 2019).

It is estimated that around 20% of symptomatic patients will be severe enough to warrant hospitalization, of which around 5% will be in intensive care.

Organ damage is multiple in Covid infection: respiratory, digestive, renal, neurological, cardiovascular due to the infection or its care. There is also a psychological and social impact of the infection or of the care that should be measured.

In this context, investigator will assess the physical and psychological complaints of patients who have presented a severe form of SARS-CoV-2 infection.

The final objective being to identify the needs to offer follow-up adapted to this emerging pathology.

Enrollment: 134 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient hospitalized for severe Covid-19 infection between March 1 and June 30, 2020 in a conventional unit, intensive care unit, at the Centre hospitalier du Mans and alive at the time of the investigation at 2 to 3 months
• Patient having given their express consent, after having received the research information letter upon discharge from hospital or having given their express consent after sending the information letter
• Age ≥ 18 years
• Patient having contracted a SARS-CoV-2 infection proved by RT-PCR and / or retrospective serology and / or a Covid-19 syndrome with suggestive chest scanner (during the period from March 1, 2020 to June 30, 2020)

Exclusion criteria

• Patient opposition to participate in the cohort
• Non-French speaking patient
• Patients who cannot read or write
• Patient subject to a protective measure
• Patient not affiliated to a social security or equivalent health insurance

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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134 participants in 1 patient group

patient hospitalized between march 1 and june 30, 2020

Experimental group

Description:

patient hospitalized between march 1 and june 30, 2020

Treatment:

Other: questionnaire