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Long Term Outcomes of Patients With COVID-19

Long Term Outcomes of Patients With COVID-19

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04360538
Acronym
COVID19 LTFU
Enrollment
500
Registered
2020-04-24
Start date
2020-04-08
Completion date
2026-11-01
Last updated
2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Corona Virus Infection, Covid-19, Critical Illness, Respiratory Failure

Keywords

long term outcomes, mechanical ventilation, noninvasive ventilation

Brief summary

The investigators hypothesize that those with respiratory failure due to COVID-19 will have different burdens of mental and physical disability than those with respiratory failure who do not have COVID-19. Detecting these potential differences will lay an important foundation for treating long term sequelae of respiratory failure in these two cohorts.

Detailed description

The aim of this proposal to is to understand the extent and degree of physical disability, psychological sequelae, and cognitive dysfunction survivors of COVID-19 related critical illness will have upon hospital discharge, 6 months, and up to one year post discharge. These outcomes of interest will be evaluated prospectively. The investigators will perform these measures in Covid-19 patients with respiratory failure and compare them to non-Covid-19 patients with respiratory failure. The investigators also seek to determine the risk factors of these long-term complications in order to guide providers as to which patients should be screened for these deficits. Finally, the investigators will examine the association of various critical care interventions such as invasive versus noninvasive mechanical ventilation or use of sedatives and their effects on disability and cognitive dysfunction.

Interventions

OTHERQuality of Life

Physical disability assessment tool

OTHERImpact Event Score

Psychological Sequelae assessment tool

OTHERHospital anxiety and depression scale

Psychological Sequelae assessment tool

Sponsors

University of Chicago
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* adult patients admitted to the ICU

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
Quality of Life scoreup to 12 months after dischargeSF-36 score

Secondary

MeasureTime frameDescription
cognitive dysfunctionup to 12 months after dischargeMontreal Cognitive Assessment (MoCA) score
Functional Status Scoreup to 12 months after discharge(FSS-ICU)
Physical Disabilityup to 12 months after dischargeMRC neuromuscular Assessment
Psychological Sequelaeup to 12 months after dischargeImpact Event Score

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 14, 2026