Covid19, Physical Disability
Conditions
Brief summary
Coronavirus disease (COVID-19) has resulted in millions of hospital admissions. The physical consequences caused by COVID-19 hospitalization could jeopardize the overall health status of patients through a decrease in functional capacity. A therapeutic exercise program may reduce the adverse effects of COVID-19 on functional capacity and thereby improve the overall health status of these patients. The objectives of this project are 1) to analyze the effect of a therapeutic exercise program in patients who have been hospitalized in Intensive Care Unit (ICU) for COVID-19. Single-blind randomized clinical trial. 118 patients post-ICU for COVID-19 will be randomized into an intervention group and a control group. The intervention group will perform a therapeutic exercise program for eight weeks in telematic modality. Functional capacity will be analyzed using the grip strength, Short Physical Performance Battery, gait speed, lower extremity strength and the FRAIL scale at baseline, eight and twelve weeks. The main statistical analysis will be a comparison of means for independent samples assessing the effect of the intervention. Given the high prevalence of patients hospitalized for COVID-19, establishing strategies to minimize the adverse effects of the virus on patients is a must for the healthcare setting. Assessing physical condition after COVID-19 will allow the magnitude of the problem to be established. Physiotherapy, through therapeutic exercise, could improve physical fitness in these patients and thus improve the overall health status after COVID-19.
Interventions
OTHERTherapeutic Exercise
Online and structured exercise therapeutic program based on flexibility, strength, balance and aerobic exercises. The program have been supervised by an expert on the field and it participants will perform it under the supervision of an expert physiotherapist.
Sponsors
Universitat Internacional de Catalunya
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age 18 years or older. * Have been diagnosed COVID-19 positive at the time of hospital admission. * Be able to use an online platform to conduct meetings with the healthcare professional or have the necessary personal assistance to do so. * Be able to read the informed consent form and understand the objectives and conduct of the study.
Exclusion criteria
* Diagnosed neurological or psychiatric disease. * Contraindications to physical exercise. * Failure to give informed consent for the study. * Unavailability to perform the ET program twice a week.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Upper limb strength change | Change from Baseline upper limb strength at 6 weeks | handgrip strength test |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Physical Performance change | Change from Baseline physical performance at 6 weeks | Short Physical Performance Battery test |
| Walking speed change | Change from Baseline walking speed at 6 weeks | 4 meters walking speed |
| lower limb strength change | Change from Baseline lower limb strength at 6 weeks | 5 times sit and reach test |
| Fraility change | Change from Baseline fraility at 6 weeks | FRAIL scale |
Countries
Spain
Outcome results
None listed