[{"arm_notes": "", "treatment_id": null, "treatment_name": "The activities will start after signing the informed consent form approved by the Research Ethics Committee. All care for the safety of the participants and the work team will be taken. First; an evaluation of the health status will be carried out. The participants who do not have limitations or discomfort that may prevent the evaluations or the intervention's performance will participate in the proposed intervention.The study design is based on a randomized controlled clinical trial composed of four groups; the control group being formed by the participants who are not available to participate in the intervention and accept to carry out a follow-up through the evaluations; and the physical training groups randomly divided according to the association of training (T) and recovery (R) with hypoxia (H) or normoxia (N): a) TH + RH; b) TN + RH; c) TN + RN. Each group will have 20 participants. The invitation will be made to Health Institutions in the region; offering the possibility of participation in this research to patients who have had moderate to severe symptoms approximately 30 days after the recovery of clinical signs or medical discharge (for those who were hospitalized). The disclosure will happen through the local television channels; USP Radio and News; social media; among other communication vehicles.The experimental protocol will consist of: i) familiarization and carrying out the initial assessments (evaluation 1) in the three sessions of week 0; ii) 8-week intervention with a partial assessment to adjust the training load between weeks 4 and 5 (half of the intervention - evaluation 2); iii) reassessments at week 9; following the end of the intervention (evaluation 3); iv) reassessments at week 13; four after the end of the intervention (eval;Other;23631", "treatment_type": "TODO", "pharmacological_treatment": "TODO"}]

[{"arm_notes": "", "treatment_id": 987, "treatment_name": "Physical exercises", "treatment_type": "Rehabilitation", "pharmacological_treatment": "Non pharmacological treatment"}, {"arm_notes": "", "treatment_id": 987, "treatment_name": "Physical exercises", "treatment_type": "Rehabilitation", "pharmacological_treatment": "Non pharmacological treatment"}, {"arm_notes": "", "treatment_id": 987, "treatment_name": "Physical exercises", "treatment_type": "Rehabilitation", "pharmacological_treatment": "Non pharmacological treatment"}, {"arm_notes": "", "treatment_id": 2188, "treatment_name": "Standard of care", "treatment_type": "Standard of care", "pharmacological_treatment": "Standard of care"}]

[{"arm_notes": "", "treatment_id": null, "treatment_name": "The activities will start after signing the informed consent form approved by the Research Ethics Committee. All care for the safety of the participants and the work team will be taken. First; an evaluation of the health status will be carried out. The participants who do not have limitations or discomfort that may prevent the evaluations or the intervention's performance will participate in the proposed intervention.The study design is based on a randomized controlled clinical trial composed of four groups; the control group being formed by the participants who are not available to participate in the intervention and accept to carry out a follow-up through the evaluations; and the physical training groups randomly divided according to the association of training (T) and recovery (R) with hypoxia (H) or normoxia (N): a) TH + RH; b) TN + RH; c) TN + RN. Each group will have 20 participants. The invitation will be made to Health Institutions in the region; offering the possibility of participation in this research to patients who have had moderate to severe symptoms approximately 30 days after the recovery of clinical signs or medical discharge (for those who were hospitalized). The disclosure will happen through the local television channels; USP Radio and News; social media; among other communication vehicles.The experimental protocol will consist of: i) familiarization and carrying out the initial assessments (evaluation 1) in the three sessions of week 0; ii) 8-week intervention with a partial assessment to adjust the training load between weeks 4 and 5 (half of the intervention - evaluation 2); iii) reassessments at week 9; following the end of the intervention (evaluation 3); iv) reassessments at week 13; four after the end of the intervention (eval;Other;Exercise;Hypoxia;Altitude", "treatment_type": "TODO", "pharmacological_treatment": "TODO"}]