COVID 19-Caregivers IGg Seroconversion

NCT ID: NCT04353323

Last Updated: 2020-05-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

130 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-05-25

Study Completion Date

2020-12-25

Brief Summary

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According to recent publications, the percentage of caregivers infected with COVID 19 is evaluated between 10 and 30% . This great variability is due, on the one hand to the intensity of the influx of covid plus patients and, on the other hand, to the disparity in the preparation of caregivers in the face of this emergency. Indeed, we can understand that the strict application of hygiene rules can be faulted in the face of the volume of patients, the lack of protective equipment and the lack of specific training for caregivers in this area. As a result, within healthcare teams, there are many questions that generate anxiety: will I be able to provide care properly while protecting myself from the risk of contamination? This anxiety is also present and sometimes manifests itself aggressively in the entourage or in the vicinity of caregivers, due to lack of scientific data adapted to the local ecology of the crisis.

Thus, the aim of this study is to show that the risk for caregivers of being contaminated by COVID in an area dedicated to COVID positive patients is no higher than being a caregiver in a non-COVID area that he either in the adult or pediatric sector.

Detailed Description

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Conditions

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Infection, COVID-19

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Covid area

Blood sampling

Intervention Type OTHER

3 blood samples (D0, D15 and D30) will be taken from each participant

Non-Covid area

Blood sampling

Intervention Type OTHER

3 blood samples (D0, D15 and D30) will be taken from each participant

Interventions

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Blood sampling

3 blood samples (D0, D15 and D30) will be taken from each participant

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* caregivers staff assigned to a non-intensive care COVID service
* or caregivers staff assigned to a non-COVID adult service
* or caregivers staff assigned to a non-COVID pediatric service
* Age \> = 18 years old
* With health insurance
* Express consent

Exclusion Criteria

* Protected persons
* Refusal to participate
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Limoges

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHU de Limoges

Limoges, , France

Site Status

Countries

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France

Central Contacts

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Laurent FOURCADE, MD

Role: CONTACT

0555058070

Facility Contacts

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Laurent Fourcade, MD

Role: primary

0555058070

[email protected]

Role: backup

Other Identifiers

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87RI20_0016/CoSigS

Identifier Type: -

Identifier Source: org_study_id

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