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Clinical Trials/NCT05619666
NCT05619666
Recruiting
Not Applicable

Acute Rehabilitation in Patients With COVID-19 Pneumonia a Single Center Experience From a Developing Country

Institut za Rehabilitaciju Sokobanjska Beograd2 sites in 1 country200 target enrollmentSeptember 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COVID-19
Sponsor
Institut za Rehabilitaciju Sokobanjska Beograd
Enrollment
200
Locations
2
Primary Endpoint
functional outcome of cardiovascular and respiratory system
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

COVID-19 can have different clinical manifestations including myalgia, arthralgia, neurological, cardiac, psychological and other manifestations.These patients are at greater risk of developing consequences of prolonged bed rest. Therefore physical medicine and rehabilitation could have an important role in the multidisciplinary treatment of these issues. Early respiratory and neuromuscular rehabilitation is necessary to improve functional physical limitations, performance, muscle strength, endurance as well as cognitive and emotional domains. Some studies proposed that rehabilitation protocols in the inpatient setting include early mobilisation, strength and endurance training with the aim of reducing weakness and dependency. This Study aimed to detect the effects of rehabilitation in patients with Covid-19 who were admitted in temporary Covid hospital in Serbia. Furthermore, to emphasize the importance of functional assessment of the patients, in identifying their problems and selections of priorities in planning the best therapeutic protocol.

Registry
clinicaltrials.gov
Start Date
September 1, 2021
End Date
January 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Institut za Rehabilitaciju Sokobanjska Beograd
Responsible Party
Principal Investigator
Principal Investigator

Tamara Filipovic

Teaching assistant

Institut za Rehabilitaciju Sokobanjska Beograd

Eligibility Criteria

Inclusion Criteria

  • Positive pharyngeal or nasal swab for SARS CoV-2, 3) SP O2\> 94% on admission, 4) body temperature under 37.5 5) Clinical stability defined by ability to perform bedside active mobilization without a reduction of oxygen saturation (SpO2) below 92%;

Exclusion Criteria

  • SP o2 \< 94% on admission, 2) Moderate and severe heart failure (grade III and IV, NY heart Association), 3) Paresis or plegia as a result of CVI or neurodegenerative disease, 4) Impaired cognitive status.

Outcomes

Primary Outcomes

functional outcome of cardiovascular and respiratory system

Time Frame: up to three weeks

six minute walk test (6MWT)

functional outcome of activity of daily living

Time Frame: up to three weeks

Bartel index (BI)

functional outcome of mobility

Time Frame: up to three weeks

"Time Up and Go" test (TUG)

functional outcome of static balance

Time Frame: up to three weeks

"One Leg Stance Test" (OLST)

functional outcome for assesing dyspnea

Time Frame: up to three weeks

Borg scale for dyspnea,

functional outcome of lower limbs strength

Time Frame: up to three weeks

"Sit To Stand" test (STS)

Study Sites (2)

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