The present prospective cohort study aims to assess factors associated with of one-year health-related quality of life and physical, cognitive and mental health outcomes among adult survivors of hospitalization for COVID-19. Adult patients requiring hospitalization due to COVID-19 disease will be followed through structured and centralized telephone interviews performed at 3, 6, 9 and 12 months after enrollment.
Study Type
OBSERVATIONAL
Enrollment
650
Hospitalization due to COVID-19
Hospital do Coração de Mato Grosso do Sul
Campo Grande, Mato Grosso do Sul, Brazil
Hospital das clínicas da UFMG
Belo Horizonte, Minas Gerais, Brazil
Hospital Emydio Germano
Belo Horizonte, Minas Gerais, Brazil
Hospital Metropolitano Célio de Castro
Belo Horizonte, Minas Gerais, Brazil
Instituto Horizonti
Belo Horizonte, Minas Gerais, Brazil
Santa Casa de Curitiba
Curitiba, Paraná, Brazil
Hospital Universitário de Londrina
Londrina, Paraná, Brazil
Hospital universitário de Ponta Grossa
Ponta Grossa, Paraná, Brazil
Hospital Universitário de Canoas
Canoas, Rio Grande do Sul, Brazil
Hospital Nelson Cornetet
Guaíba, Rio Grande do Sul, Brazil
...and 14 more locations
One-year utility score of health related quality of life
The outcome will be assessed using the Brazilian version of the Euroqol-5D-3L (EQ-5D3L) questionnaire.
Time frame: The outcome will be assessed 12 months after enrollment.
Utility score of health related quality of life at 3, 6, and 9 months
The outcome will be assessed using the Brazilian version of the Euroqol-5D-3L (EQ-5D3L) questionnaire. The utility score derived from the EQ5D-3L ranges from 0 (death) to 1 (perfect health).
Time frame: The outcome will be assessed at 3, 6, and 9 months after enrollment.
Incidence of all-cause mortality
Incidence of all-cause mortality
Time frame: The outcome will be assessed at 3, 6, 9, and 12 months after enrollment.
Incidence of major cardiovascular events
Incidence of major cardiovascular events (composite endpoint of non-fatal stroke, non-fatal acute myocardial infarction, or cardiovascular death)
Time frame: The outcome will be assessed at 3, 6, 9, and 12 months after enrollment.
Incidence of rehospitalizations
Incidence of all-cause rehospitalizations
Time frame: The outcome will be assessed at 3, 6, 9, and 12 months after enrollment.
Prevalence of prolonged COVID-19 symptoms
Prevalence of prolonged COVID-19 symptoms defined as presence of dyspnea, cough, fatigue, muscular weakness, chest discomfort, joint pain, anosmia, hair loss, brain fog, insomnia, among others)
Time frame: The outcome will be assessed at 3, 6, 9, and 12 months after enrollment.
Prevalence of cognitive dysfunction
Prevalence of cognitive dysfunction as assessed by the Telephone Interview for Cognitive Status (TICS-m; scores ranging from 0 to 50 with lower scores indicating worse cognition).
Time frame: The outcome will be assessed at 3, 6, 9, and 12 months after enrollment.
Prevalence of anxiety and depression symptoms
Prevalence of anxiety and depression symptoms as assessed by the Hospital Anxiety and Depression Scale (anxiety and depression scores range from 0 to 21, with higher scores indicating worse symptoms).
Time frame: The outcome will be assessed at 3, 6, 9, and 12 months after enrollment.
Prevalence of posttraumatic stress disorder symptoms
Prevalence of posttraumatic stress disorder symptoms as assessed by the Impact Event Scale-6 (scores range from 0 to 24 with higher scores indicating worse symptoms).
Time frame: The outcome will be assessed at 3, 6, 9, and 12 months after enrollment.
Physical functional status
Physical functional status as assessed by the modified Barthel index (score ranges from 0 to 100; higher scores indicate less functional dependence).
Time frame: The outcome will be assessed at 3, 6, 9, and 12 months after enrollment.
Instrumental Activities of Daily Living
The outcome will be assessed using the Lawton \& Brody Instrumental Activities of Daily Living Scale (the score ranges from 0 to 8, with higher scores indicating less dependence).
Time frame: The outcome will be assessed at 3, 6, 9, and 12 months after enrollment.
Incidence of return to work or study
Incidence of return to work or study among patients that were working or studying at the moment of hospitalization.
Time frame: The outcome will be assessed at 3, 6, 9, and 12 months after enrollment.
Incidence of new symptomatic COVID-19 infection
Incidence of new symptomatic COVID-19 infection defined as recurrence of COVID-19-related symptoms with a positive PCR test for SARS-CoV-2 90 days after the index infection.
Time frame: The outcome will be assessed at 3, 6, 9, and 12 months after enrollment.
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