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Clinical Trials/NCT04412265
NCT04412265
Completed
Not Applicable

Relationship Between Frailty and Clinical Outcomes in Elderly Patients With COVID-19

University of Milano Bicocca6 sites in 1 country1,344 target enrollmentApril 16, 2020
ConditionsCovid19

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Covid19
Sponsor
University of Milano Bicocca
Enrollment
1344
Locations
6
Primary Endpoint
Development of a tool to measure frailty
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

This is a multicentric retro-prospective observational study that wants to evaluate the relation between frailty and clinical outcomes in elderly patients with COVID-19.

Detailed Description

BACKGROUND: Assessment of frailty is today the best way to evaluate the biological age of the elderly person. Fragility can be defined as a syndrome selected by the reduction of organized reserves and by the decreased resistance to "stressors", resulting from the cumulative decline of multiple physiological systems that cause vulnerabilities and adverse consequences. The impact of fragility on clinical outcomes has been investigated in numerous studies conducted on elderly patients in various care setting, proving in all of them a significant and more reliable predictor of variables such as age, comorbidity and individual pathologies, short and long-term mortality, length of stay and the onset of complications. Previous studies have already shown that frail older adults have a greater susceptibility to viral infections (including non-COVID-19 coronavirus) due to a malfunction of their immune system. The identification of fragility could therefore be particularly useful for identifying subjects at risk of negative outcomes (worsening of respiratory parameters, need for intubation, mortality) even in a ward with COVID + patients. In other words, the imperceptible clinical heterogeneity behind the age parameter could be better represented by a multidimensional parameter capable of measuring the accumulation of age-related deficits. SAMPLE SIZE (n. patients): The study plans to recruit 30 subjects per week on average; for an expected total of about 300 subjects for each participating site. STUDY DESIGN: The patient will be enrolled in the study when obtaining consent. In this phase the following data will be collected: * date of birth * gender * demographic data * comorbidity * Brescia_COVID respiratory scale * modified Early Warning Score * delirium * data relating to functional autonomy * blood chemistry data at the entrance. Using the variables that are part of the Comprehensive Geriatric Assessment, it will be possible to calculate the Frailty Index (FI), according to the Rockwood deficit accumulation model. A series of variables will then be collected relating to treatment procedures, therapies, the team's choice to maximize the care ceiling for the individual patient and the patient's clinical outcome. Patients will be treated as per Normal Clinical Practice; no blood chemistry tests will be required in addition to the panel of tests provided by the hospital's health management for all patients with COVID-19. Given the difficulty in systematically obtaining written informed consent and given the great public interest of the project, the research will be conducted in the context of the authorizations guaranteed by Article 89 of the GDPR EU Regulation 2016/679, which guarantees the treatment for purposes of public interest, scientific or historical research or statistical purposes of health data. STATISTICAL ANALYSIS: The FI will be built according to the Rockwood deficit accumulation model, taking into account a minimum number of variables that are part of the Comprehensive Geriatric Assessment. The FI will be obtained from the ratio between the number of pathological conditions present and the total number of indicators evaluated. Data from patients older than 60 years of age will be compared.

Registry
clinicaltrials.gov
Start Date
April 16, 2020
End Date
December 15, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Development of a tool to measure frailty

Time Frame: Until patient discharge from the hospital (approximately 1 year).

The aim of the project is to evaluate whether a tool built to measure frailty in elderly patients admitted to the COVID + hospital wards is more accurate in predicting clinical states than a clinical evaluation developed on age and comorbidity.

Secondary Outcomes

  • A "proxy" variable of the fragility index can be built on the basis of regional administrative databases only.(Until patient discharge from the hospital (approximately 1 year).)
  • Give elements to focus the screening policies for COVID19.(Until patient discharge from the hospital (approximately 1 year).)
  • Give the prevention of contagion at the elderly population level.(Until patient discharge from the hospital (approximately 1 year).)

Study Sites (6)

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