COVID-19
Conditions
Keywords
COVID-19, Muscle Strength, pulmonary function, Physical activity, Dyspnea
Brief summary
The coronavirus disease 2019 (COVID-19) is a highly contagious disorder caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). COVID-19 is a multisystem disease and therefore presents a variety of symptoms in the acute phase, such as fever, dry cough, fatigue, sore throat, loss of taste or smell, shortness of breath, nasal congestion, chest pain, muscle or joint pain, headache, and nausea. COVID-19 primarily affects the respiratory functions of individuals. Although this situation is more difficult in hospitalized patients, it also causes severe effects in individuals who recover with home medication. It is thought that this damage caused by COVID-19 may cause permanent effects on individuals in the long term. During the COVID-19 period, individuals also had to maintain an inactive lifestyle due to quarantine. This decrease in physical activity capacity also causes permanent damage to the respiratory functions of individuals. In addition, studies have focused on this population, as COVID-19 usually affects older individuals. However, considering that young people are also exposed to the COVID-19 virus, the effect on respiratory functions in these individuals should also be examined. Combined with the available information on pulmonary functions, there is insufficient evidence about extrapulmonary features in post-COVID-19 patients who survive mild illness in the long term. It is also necessary to examine whether there is permanent damage to extrapulmonary features such as peripheral muscle strength in these individuals. Therefore, in our study, it is aimed to examine the long-term results of respiratory functions, respiratory muscle strength and peripheral muscle strength of young individuals who recovered from COVID-19 and recovered from mild disease.
Interventions
None listed
Sponsors
Karabuk University
Study design
Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to 25 Years
Healthy volunteers
Yes
Inclusion criteria
Patients: * diagnosed with COVID-19, with a positive polymerase chain reaction (PCR) test * at least six months ago (long term) * non-hospitalization due to COVID-19 * non-smoker / for ex-smokers with 10 pack x years or less of smoking * not continuing any regular physical activity program Controls: * non-smoker / for ex-smokers with 10 pack x years or less of smoking, * not continuing any regular physical activity program * willing to participate to the study
Exclusion criteria
* receiving inpatient or intensive care treatment due to COVID-19 * having acute infection * previous pulmonary resection or cardiac surgery * having lung or heart comorbidities such as asthma * chronic obstructive pulmonary disease (COPD) and heart failure * uncontrolled hypertension * history of malignancy * neurological disease (e.g., Alzheimer, Multiple Sclerosis, Parkinson) * rheumatologic diseases
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Respiratory Muscle Strength | First Day | Maximal inspiratory and expiratory muscle strength will be evaluated using portable mouth pressure device. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pulmonary function (Forced vital capacity (FEV1)) | First Day | Pulmonary function (Forced expiratory volume in the first second (FEV1)) \[ Time Frame: First Day \] Pulmonary function will be evaluated with the spirometry. Dynamic lung volume measurements will be made according to American Thoracic Society and European Respiratory Society criteria. With the device, forced expiratory volume in the first second (FEV1) will be evaluated. |
| Pulmonary function (FEV1 / FVC) | First Day | Pulmonary function will be evaluated with the spirometry. Dynamic lung volume measurements will be made according to American Thoracic Society and European Respiratory Society criteria. With the device, FEV1 / FVC will be evaluated. |
| Pulmonary function (Flow rate 25-75% of forced expiratory volume (FEF 25-75%)) | First Day | Pulmonary function will be evaluated with the spirometry. Dynamic lung volume measurements will be made according to American Thoracic Society and European Respiratory Society criteria. With the device, flow rate 25-75% of forced expiratory volume (FEF 25-75%) will be evaluated. |
| Pulmonary function (Peak flow rate (PEF)) | First Day | Pulmonary function will be evaluated with the spirometry. Dynamic lung volume measurements will be made according to American Thoracic Society and European Respiratory Society criteria. With the device, peak flow rate (PEF) will be evaluated. |
| Pulmonary function (Forced vital capacity (FVC)) | First Day | Pulmonary function will be evaluated with the spirometry. Dynamic lung volume measurements will be made according to American Thoracic Society and European Respiratory Society criteria. With the device, forced vital capacity (FVC) will be evaluated. |
| Post-COVID-19 Functional Status | First Day | The post-COVID functional status of individuals recovering from COVID-19 will be evaluated with the Post-COVID-19 Functional Status Scale (PCFS). A minimum of 0 (no functional limitations) and a maximum of 5 (death) points are taken from this scale, and as the score increases, the functional status worsens. |
| Shortness of breath | First Day | The Modified Borg Scale will be used to determine dyspnea perception during rest and activity. |
| Fatigue | First Day | The Modified Borg Scale will be used to assess fatigue. The lowest 0 points are not at all and the highest 10 points are very severe denoting fatigue |
| Physical Activity | Second Day | Physical activity levels will be used assessed using International Physical Activity Questionnaire. Physical activity levels are classified as physically inactive (\<600 MET min/week), low physical activity level (600-3000 MET min/week), and adequate physical activity level (\>3000 MET min/week). |
| Peripheral Muscle Strength | Second Day | Knee extensor muscle strength using portable hand held dynamometer will be evaluated. |
Countries
Turkey (Türkiye)
Outcome results
None listed