Geriatric Population COVID-19 Observational Study (GEROCOVIDobs)

  • STATUS
    Recruiting
  • participants needed
    1500
  • sponsor
    Raffaele Antonelli Incalzi
Updated on 19 February 2024
dementia
covid-19
SARS
acute respiratory syndrome (sars)

Summary

The GeroCovid e-Registry is a European de-identified clinical data electronic registry of geriatric patients at risk or suffering from COVID-19 (suspected and confirmed cases) observed since 1st March 2020 in the participating investigational sites.

Description

Older adults ( 65 years) and pre-geriatric population (60 years and <65 years) are the ones most at risk from complications of COVID-19, including increased mortality, possibly in relationship with their comorbidity and frailty status.

The GeroCovid e-registry is intended to track Covid-19 pandemic impact on the general geriatric population and on age/care-setting related sub-populations.

The analysis of results is expected to facilitate the adoption of optimal standard of geriatric care during the pandemic.

Details
Condition Covid 19
Age 60-100 years
Clinical Study IdentifierNCT04379440
SponsorRaffaele Antonelli Incalzi
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Applying only to the " Acute Ward Patients " cohort
Hospitalised patients
Suspected or known SARS-CoV-2 infection
Applying only to the "Nursing Homes (RSA)" cohort
Nursing Home Resident Older Adults
Suspected or known SARS-CoV-2 infection
Applying only to the" Home and outpatients' care " cohort
Outpatients at risk of SARS-CoV-2 infection
Applying only to the" Dementia outpatients " cohort
Outpatients suffering from dementia according to NIA-AA criteria
At risk of SARS-CoV-2 infection
Ongoing treatment with anti-cholinesterase- dugs and/or anti-psychotics
Applying only to the" At home " cohort
Outpatients at risk of SARS-CoV-2 infection
Applying only to the " Outcomes " cohort
Age65 years
Hospitalised patients diagnosed with SARS-CoV-2 infection

Exclusion Criteria

Lack of a signed Informed Consent if the patient received and understood the information about the study
Lack of a signed declaration by the responsible physician stating that no explicit opt-out advanced directives by the subject were known to be in place at the moment of inclusion if it had been impossible to inform the patient due to her/his state of consciousness and/or awareness of disease condition
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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