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Short-term Physical Function Outcomes in Severe COVID-19 Patients Admitted to ICU for Invasive Mechanical Ventilation

Short-term Physical Function Outcomes in Severe COVID-19 Patients Admitted to ICU for Invasive Mechanical Ventilation: an Observational Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04400461
Enrollment
71
Registered
2020-05-22
Start date
2020-05-15
Completion date
2021-03-01
Last updated
2021-04-13

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

Conditions

COVID-19

Keywords

physical function, functional outcomes, strength, intensive care unit, rehabilitation

Brief summary

Little is known about the physical function outcomes in patients with severe COVID-19 patients who are admitted to Intensive Care Unit (ICU) for invasive mechanical ventilation. The purpose of this study is to evaluate the short-term impact on physical function before hospital discharge in subjects with severe COVID-19 who have survived ICU admission for invasive mechanical ventilation.

Detailed description

DESIGN: An observation cohort study conducted in a tertiary hospital. METHODS: Data will be collected from patients along the ICU-hospital discharge continuum, will be analysed and non-parametric tests will be used to explore association between variables. Outcome measures: Muscle strength, as a component of physical function, will be evaluated with the Medical Research Council sum score (MRC- SS) at discharge from ICU and at hospital discharge; the Functional Status Score for the ICU (FSS-ICU) will also be assessed at hospital discharge. Data on participants' demographics, ICU admission and hospital admission will also be collected. SIGNIFICANCE OF THE RESEARCH: Understanding how physical function is affected in patients with severe COVID-19 may help develop future prevention, therapeutic and follow-up strategies that improve quality of care and outcomes in this specific group of patients. Findings from this study may be useful to design future larger cohort studies and experimental trials.

Interventions

Clinical Testing: muscle strength. Muscle strength, as a component of physical function, will be assessed with the Medical Research Council sum score (MRC- SS) at discharge from the ICU and at discharge from the hospital. Clinical testing: physical function. The Functional Status Score for the ICU (FSS-ICU) will be used to evaluate 5 functional tasks at discharge from hospital.

Sponsors

Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years

Inclusion criteria

* subjects diagnosed with COVID-19 who have required admission to ICU for invasive mechanical ventilation; * have received invasive ventilation \> 24 hours; * have been successfully weaned from mechanical ventilation \> 48 hours; * were independently able to mobilise prior to current hospital admission (this includes subjects who used a walking stick or another gait aid to mobilise.

Exclusion criteria

* subjects or proxies with inability to communicate in Spanish fluently; * cognitive impairment prior to ICU admission; * proven neurological impairment or neuromuscular disorder; * Cerebrovascular Accident during hospital stay; * previous organ transplant; * pregnancy; * unstable fractures or any other injuries that would require medical bed rest.

Design outcomes

Primary

MeasureTime frameDescription
Medical Research Council sum score (MRC- SS).< 48 hours before ICU dischargePhysical examination will be performed to carry out manual muscle testing of strength in 6 different muscle groups of the upper limb and lower limb on both sides of the body.
The Functional Status Score for the ICU (FSS-ICU)< 24 hours before hospital dischargeThe Functional Status Score for the ICU (FSS-ICU) will be used to evaluate 5 functional tasks. Each task is evaluated using an 8-point ordinal scale ranging from 0 (not able to perform) to 7 (complete independence).The total FSS-ICU score ranges from 0 to 35, with higher scores indicating better physical functioning.

Secondary

MeasureTime frameDescription
Body Mass IndexThroughout study completion, up to 6 monthskg/m2
Baseline mobilityFirst day the patient can cooperate with assessment according to the ' 5 Standard Questions' test.Baseline mobility
APACHE II score<24 hours after ICU admissionAcute Physiology and Chronic Health Evaluation II score.The APACHE II score ranges from 0 to 71 points. Higher scores correspond to more severe disease and a higher risk of death.
Length of stay in ICUThroughout the study completion, up to 6 monthsNumber of days of stay in ICU
Number of days on mechanical ventilationThroughout the study completion, up to 6 monthsNumber of days on mechanical ventilation
AgeThrough study completion, up to 6 monthsAge in years
Number of days on Neuromuscular BlockersThroughout the study completion, up to 6 monthsNumber of days on NMB during mechanical ventilation
Episodes of prone positioningThroughout the study completion, up to 6 monthsNumber of prone positioning episodes during ICU stay
Length of stay in hospitalThroughout the study completion, up to 6 monthsTotal number of days admitted to hospital
Continuation of careThroughout the study completion, up to 6 monthsHome with no follow-up physiotherapy, home with domiciliary or out-patient physiotherapy, rehabilitation facility, care home, transfer to another acute hospital.
Polyneuropathy diagnosisThroughout the study completion, up to 6 monthsClinical or EMG polyneuropathy diagnosis confirmation
SexThroughout study completion , up to 6 monthMale vs Female

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026