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Functional Outcomes in COVID-19 Survivors and Use of a Digital Platform for Rehabilitation

Functional Outcomes in COVID-19 Survivors and Use of a Digital Platform for Rehabilitation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04695301
Enrollment
25
Registered
2021-01-05
Start date
2020-07-01
Completion date
2021-10-01
Last updated
2022-02-11

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

Conditions

Coronavirus Infections, COVID-19, Exercise Therapy

Keywords

Telemedicine, exercise therapy, coronavirus infections, stress disorders traumatic, fatigue, quality of life

Brief summary

COVID-19, an acute respiratory disease caused by coronavirus-2 (SARS-CoV-2), and in most cases, causes mild to moderate symptoms of fever, cough and dyspnea. However, a not insignificant portion, given the total number of people affected, will present symptoms of severe acute respiratory failure and multiple organ failure, requiring hospitalization under intensive care, use of mechanical ventilation, prolonged period of immobilization and, consequently, physical, cognitive and psychological damage, which may affect survivors for a long period after hospitalization. All of these factors are known to have an impact on various areas of life: personal, social and economic, which makes the need for continued specific care after hospital discharge relevant. In this context, the role of rehabilitation programs is fundamental, aiming not only at a safer dehospitalization, but also at the continuity of care with the objective of restoring the biopsychosocial skills of these individuals, allowing functional independence for activities of daily life and a shorter return physical and social activities performed before the disease. However, the big challenge for the health system is how to offer this on a large scale. Therefore, knowing the clinical and functional profile of these patients at discharge and verifying the viability of a digital platform for rehabilitation and monitoring of these patients is the first step to allow the creation of a new form of continuity of care and access to affected patients with serious diseases such as COVID-19 and other syndromes capable of generate functional impairment. Therefore,the investigators objective is to characterize and monitor the functional profile and exercise capacity of patients affected by COVID-19 at the hospital discharge, as well as to verify the viability and compliance of patients to the use of a digital platform for the application of a distance rehabilitation program.

Detailed description

The investigators proposal is to characterize and evaluate the impact of the disease on the clinical, functional and social aspects in these patients affected by COVID-19 and to propose the continuity of specific care after hospital discharge with a physical rehabilitation program through a digital platform, remotely for a period of 3 months. The proposed hypothesis is that patients convalescing from COVID-19 and undergoing the rehabilitation program will have a gain in functional skills and quality of life. The professional team involved in this study will be responsible for managing, monitoring and evaluating the participating patients and monitoring the performance of the proposed functional exercises.

Interventions

OTHERRehabilitation protocol through a digital platform

During 3 months the patients will participate in a rehabilitation program through a digital platform

Sponsors

Hospital Israelita Albert Einstein
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Subject)

Intervention model description

Men and women affected by COVID-19, over 18 years of age, admitted to HIAE partner hospitals who have been in hospital for more than 10 days or in need of treatment in semi-intensive or intensive care units will be selected. Follow-up will be carried out for 3 months, with remote reevaluations. During this period, the rehabilitation program will be offered for 3 months, through a digital platform.

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Men and women affected by COVID-19 * over 18 years of age, admitted to HIAE partner hospitals

Exclusion criteria

* presence of a physical or cognitive condition that makes it impossible or contraindicated to perform the 2-minute stride test and perform the proposed exercises. * Patients with a more severe clinical and functional profile, * Pregnant women

Design outcomes

Primary

MeasureTime frameDescription
Characterize the clinical function profile of patients affected by COVID-193 monthsCharacterize the clinical functional profile of patients affected by COVID-19 by data from medical records
Characterize the exercise capacity of patients affected by COVID-193 monthsCharacterize the exercise capacity of patients affected by COVID-19 by 2-minute step test

Secondary

MeasureTime frameDescription
Assess clinical and demographic data3 monthsAssess clinical and demographic data
Assess functional level at hospital discharge3 monthsAssess functional level at hospital discharge and 3 months after discharge by physical test
Assess patient compliance of the rehabilitation program using the digital platform3 monthsAssess patient compliance of the rehabilitation program using the digital platform checking your adherence to the program

Countries

Brazil

Outcome results

None listed

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