Safety evaluations will be conducted at screening, throughout the trial, and at follow-up 12 weeks after the last TCMRE, although TCMRE programs are low risk. Any adverse events (AEs) will be collated from CRFs and follow-up questionnaires. Even though BT and KQG are at low risk. AEs will be collated from CRFs and follow-up questionnaires. Researchers will then analyze whether AEs are directly related to the rehabilitation program. When sports injuries occur or condition suddenly deteriorates during the trial with serious complications or severe adverse effects such as breathing difficulties, severe anxiety, severe depression, the trial will be terminated immediately and prompt medical treatment will be administered according to the condition of the subject. Researchers will then analyze whether they are directly related to the rehabilitation program.
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