COVID-19 Prevalence in UNIVI Geriatric Institutions: Epidemiological Study of Immunological Status With Rapid Serological Tests

NCT ID: NCT04790994

Last Updated: 2021-03-10

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 1145 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2020-07-24
• Study Completion Date: 2021-04-16

Brief Summary

To date, little information is available on the prevalence of Covid-19 and data are lacking on the proportion of patients, institutional residents and caregivers who have actually been exposed to SARS Cov-2.

With the NG Biotech rapid serological test, an individual's immunological status (presence of IgM and IgG antibodies) can be determined in 15 minutes on a finger-prick blood sample.

The proposed trial will be a noninterventional study of immunological status among the residents and caregivers of 26 nursing homes and 4 geriatric healthcare institutions belonging to the UNIVI Group who are representative of the institutional geriatric population in France. The NG Biotech rapid test will be carried out concomitantly with polymerase chain reaction (PCR) tests performed within the framework of a national screening campaign. Data on risk factors in staff members and on specific COVID 19 symptoms in residents will also be collected.

The study will terminate for residents and caregivers whose tests are both negative (absence of infection and no exposure to the virus). For residents and caregivers who have at least one positive test, follow-up visits will be scheduled in order to study the serology time course and the occurrence of reinfection (follow-up questionnaire).

Detailed Description

Type of study: multicentric prospective observational Study location: 26 nursing homes and 4 geriatric hospitals belonging to the UNIVI Group in France

Context:

At the end of the Covid-19 containment period in France, data published by Public Health France revealed that frail and dependent elderly people in nursing homes and geriatric healthcare institutions had paid a heavy tribute. As of May 4, 2020, the majority of reported Covid-19 cases (n=4,600; 63%) had occurred in nursing home residents and more than one-third (n=2,664; 37%) in patients in geriatric healthcare institutions. A total of 71,216 Covid-19 cases of which 33,948 (48%) were confirmed by reverse transferase polymerase chain reaction (RT-PCR) tests were reported to health authorities (Agence Régionale de Santé, ARS). Among reported cases, there were 12,726 deaths. Three-quarters of these deaths (9,501; 75%) occurred in geriatric institutions, the vast majority (99%) in nursing homes and 3,321 (25%) in hospitals. Reports of infection among staff members of these institutions reached 39,294 cases, of which 18,175 (46%) were confirmed by RT- PCR.

The confinement allowed a significant and continuous decrease in the number of Covid cases in French geriatric institutions since the beginning of April. The proportion of new cases observed among institutionalized geriatric residents has since fallen sharply, particularly in the most affected geographic regions. This is why deconfinement should be gradual and should be constantly reassessed on the basis of national and regional epidemiological data. Each nursing home should to take into account its own daily data showing the number of new diagnoses or suspected cases among residents and caregivers, keeping in mind the risk of transmission by visitors in the event of a recurrence of the epidemic.

In France, the deconfinement strategy began on April 20, 2020 in Île-de-France. Family visits under strict conditions were authorized in geriatric institutions. Currently, the modus operandi is accompanied by a PCR test campaign in order to have an inventory of the COVID status of all institutional residents and caregivers. Thus, any resident with a positive PCR test will be isolated until recovery and any caregiver with a positive PCR test will be quarantined.

For nursing home admissions, in accordance with ARS guidelines, a PCR test may be requested upon prescription from the institution's coordinating physician. Room confinement for newly admitted residents will be determined by the institution's geographical localization. Administrative districts are classified in two zones, red and green. For institutions in the red zone, room confinement with close medical supervision is compulsory for 14 days, corresponding to the viral incubation time. For institutions in the green zone, room confinement is not mandatory, but close medical surveillance is recommended.

What could NG Biotech rapid serological tests bring to the deconfinement strategy? These tests make it possible to determine an individual's immunological status (presence of IgM and IgG antibodies) in 15 minutes on a finger-prick blood sample. The test cannot be used in the acute phase of the disease, but makes it possible to confirm the serological status of an asymptomatic patient 15 days after the first clinical signs. Test sensitivity (ability to identify antibodies) is 100%. Serological testing does not answer the same question as PCR. PCR directly detects the presence of the virus, optimal in the first 7 days, it can remain positive for up to 3 weeks or even beyond. The serological test provides information on whether or not there is contact with the virus. If the serological test is positive in an asymptomatic patient, the patient is likely more than 15 days from symptom onset. It does not provide information on the risk of contagiousness. For nursing homes and geriatric healthcare institutions, use of serological testing, common law is applicable. The superior French health agency (Haute Autorité de Santé, HAS) specifies that these tests are indicated for epidemiological study or as a diagnostic catch-up tool (Place of rapid serotests in the strategy for the management of the COVID-19, HAS, May 14, 2020). The HAS recommendation specifies that rapid diagnostic tests must be performed by: - Professionals and staff who have previously received training in the use of COVID-19 rapid diagnostic tests - Doctors practicing in private practice - Doctors, medical biologists, midwives working in an institution or in a healthcare service (e.g. specialized screening structures) - Nurses or laboratory technicians working in an institution or in a healthcare service under the supervision of a doctor or a medical biologist - Midwives or nurses working in a prevention structure or an associative structure involved in health prevention - Community pharmacists - Employees or volunteers, non-healthcare professionals working in a prevention structure or an association structure, provided that they have previously received training in the use of rapid diagnostic tests.

To date, little information is available on the prevalence of Covid-19 and data are lacking on the proportion of patients, institutional residents and caregivers who have actually been exposed to SARS Cov-2. Likewise, in the scientific literature, there is uncertainty among people who have acquired immunity as to the persistence of neutralizing antibodies at 6 months and the risk of re-infection with COVID 19 after a primary infection. A major campaign of serological tests is in preparation in the geriatric institutions of the UNIVI Group. This study is based on this campaign using data collected in 26 nursing homes and 4 geriatric healthcare institutions. In total, around 2,000 residents, and 2,000 caregivers will be tested. The residents and caregivers of the tested institutions are representative of the institutionalized geriatric population in France. It is thus proposed to carry out a non-interventional study among residents and caregivers in nursing homes and in healthcare institutions belonging to the UNIVI Group. NG Biotech rapid tests will be performed concomitantly with PCR tests made within the framework of the national screening campaign.

Conditions

COVID-19

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Residents of participating nursing home - who benefited from a rapid diagnostic orientation serological test for COVID-19 - having given their agreement
• All staff members (doctors, nurses, health executives, caregivers, physiotherapists, ASH, stretcher bearers, psychologists, dieteticians, administrative staff, secretaries, ...) - who benefited from a rapid diagnostic orientation serologic test for COVID-19 - having given their agreement

Exclusion Criteria

• Refusal to participate

• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Centre Médical Porte Verte

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

CentreMédicalPorteVerte

Versailles, , France

Countries

France

Other Identifiers

2020-A01838-31

Identifier Type: -

Identifier Source: org_study_id