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Completed

NCT Number: NCT04677283

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.

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Autonomy Department; ARS Île-de-France

Paris, ARS Île-de-France, 75019, France

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • / Residents of nursing homes in Île-de-France in which systematic Covid-19 screening tests were carried out and agreeing to participate in the study.
  • / Professionals in nursing homes in Île-de-France in which systematic screening tests for Covid-19 were carried out and agreeing to participate in the study: nursing assistants, nurses, coordinating doctors, hotel and service agents hygiene, etc.

Exclusion criteria

  • / Expression of opposition to the collection of symptoms by professionals, residents or their legal representatives.
  • / Subjects who have not had a diagnostic test by RT-PCR.

Treatment and study plan

Primary outcomes

  1. To define positive cases of coronavirus by "Polymerase Chain Reaction" results and symptomatologies

    Time frame: 3 Months

Secondary outcomes

  1. Assessment of commorbidity risk according Charlson score

    Time frame: 3 Months

  2. Assessment of patient's level of dependence through an appreciation of instrumental activities of daily living according Lawton scale

    Time frame: 3 Months

  3. Assessment of teh degree of autonomy according AGGIR score

    Time frame: 3 Months

  4. Measuring cognitive impairment according Mini-Mental State Examination (MMSE) scores

    Time frame: 3 Months

  5. Screening for a nutritional disorder according Body Mass Index (BMI) score

    Time frame: 3 Months

Sponsors and collaborators

Lead sponsor

Gérond'if

Other

Registry information

Acronym: COVID - EHPAD

Important dates

Study start
2020
Primary completion
2020
Study completion
2021
First posted
Dec 21, 2020
Registry last updated
Feb 14, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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