Clinical Trials Directory

Trials / Completed

CompletedNCT04677283

Study of Symptoms Linked to Covid-19 in Residents and Professionals in EHPAD, Associated With a Dual Diagnostic Approach by PCR and Serology: a Cohort in Île-de-France.

Status
Completed
Phase
Study type
Observational
Enrollment
1,059 (actual)
Sponsor
Gérond'if · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The main purpose is to study the prevalence of Covid-19 in EHPAD. The primary endpoint will be the combination of PCR results and symptomatology, making it possible to define positive cases in EHPAD, in residents and professionals in contact with them. The prevalence obtained can be compared with the results of serology if these are performed.

Detailed description

This study is taking place in several nursing homes in Ile-de-France, which will be recruited at the end of the diagnostic campaign. At the initiative of the ARS Ile-de-France, residents and professionals of selected EHPADs will be subjected to systematic screening by RT-PCR for Covid-19, then by serology after the first screening, regardless of whether either the result Samples, by nasopharyngeal swab for RT-PCR, by capillary blood sampling or venipuncture according to the technique for serology, will be carried out according to the doctrines issued by the ARS Ile de France and the variations proposed by the appropriate departmental directorates in depending on local resources. The results will be brought to the attention of EHPADs to adapt the care of residents and positive professionals. Data will be collected daily from collection for the first test (RT-PCR), or retrospectively if the collection took place before the study. Regarding the approach for collecting serologies: * All subjects included with a negative PCR will be offered the serological test, in accordance with the recommendations in force or the medical decisions of the establishments. * The qualitative results of the serologies of the subjects included in the study (residents and professionals) will be collected according to the same circuit as those of the RT-PCRs. * Only the symptoms of residents with a positive serology will be collected, from the date of the sample and for a period of 14 days. * The symptoms of professionals with a positive serology can be collected, from the date of the sample and for a period of 14 days without mandatory character. * Both techniques (ELISA or TROD) are accepted and the serology values will not be collected.

Conditions

Timeline

Start date
2020-05-07
Primary completion
2020-12-09
Completion
2021-07-08
First posted
2020-12-21
Last updated
2023-02-14

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04677283. Inclusion in this directory is not an endorsement.