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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04751630
Other study ID # CBAS-21-22
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2021
Est. completion date March 1, 2022

Study information

Verified date March 2022
Source Universitat Internacional de Catalunya
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date March 1, 2022
Est. primary completion date February 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Therapeutic 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.

Locations

Country Name City State
Spain Hospital Arnau de Vilanova Lleida

Sponsors (1)

Lead Sponsor Collaborator
Universitat Internacional de Catalunya

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Upper limb strength change handgrip strength test Change from Baseline upper limb strength at 6 weeks
Secondary Physical Performance change Short Physical Performance Battery test Change from Baseline physical performance at 6 weeks
Secondary Walking speed change 4 meters walking speed Change from Baseline walking speed at 6 weeks
Secondary lower limb strength change 5 times sit and reach test Change from Baseline lower limb strength at 6 weeks
Secondary Fraility change FRAIL scale Change from Baseline fraility at 6 weeks
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