COVID-19
Conditions
Interventions
This project was divided into three studies as presented in the method described below. The sample will consist of 100 participants of both sexes, aged 18 to 75 years. Participants will be allocated f
BRUGLIERA et al., 2020). However, participants with more than three absences will be discontinued from the program. All sessions will be supervised by physiotherapists trained for their procedure. Th
E02.760.169.063.500.387.875
Sponsors
Universidade Presbiteriana Mackenzie
Universidade Presbiteriana Mackenzie
Eligibility
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Both sexes; aged 18 to 75 years; normal or corrected vision; with previous diagnosis of COVID-19; Only for study 3 - the participant needs to be clinically stable; oxygen saturation > 93%; respiratory rate of at least 12-20 breaths per minute (pmI); heart rate of 60 to 110 breaths per minute (bpm)
Exclusion criteria
Exclusion criteria: participants who have inability to fully or fully understand the instruments used in this project; participants with myopathies; diseases with peripheral demyemyellinization; malnutrition; neoplasms in treatment; anorexia; chronic kidney diseases; liver disease; or any other disease that promotes sarcopenia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Significant improvement in functional capacity is expected when compared before and after the intervention period, through the tests: Sit and Stand up and Timed Up and Go (TUG);Significant improvement in the strength of the muscles worked is expected when compared before and after the treatment period, by means of the maximum repetition 1 test (1RM);It is expected to find a reduction in fatigue and pain, when compared before and after the treatment period, through the fatigue assessment scale and the visual analog scale (VAS); | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to improve the subjective perception of quality of life after COVID, when compared before and after the treatment period, through the EQ-5D questionnaire, especially in the domains of physical and mental health;;A significant improvement in sleep quality is expected when compared before and after the intervention, using the Pittsburgh questionnaire. | — |
Countries
Brazil
Contacts
Public ContactMarília Coelho
Universidade Presbiteriana Mackenzie
Outcome results
None listed