The goal of this clinical trial is to determine whether Qi-Gong can improve physiological function and quality of life (QoL) in individuals with post-acute sequelae of SARS-CoV-2 infection (PASC). Study Objectives: To assess whether Qi-Gong improves physiological function in individuals with PASC. To evaluate whether Qi-Gong enhances quality of life in individuals with PASC. Study Design: If a comparison group is included, researchers will compare Qi-Gong with standard care to assess its effectiveness. Participant Involvement: Practice Qi-Gong three times per week for three months. Record physiological data monthly.
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Pulmonary Function Test (Forced vital capacity)
Timeframe: From enrollment to the end of treatment at 12 weeks
Pulmonary Function Test (FEV1)
Timeframe: From enrollment to the end of treatment at 12 weeks
Pulmonary Function Test (FVCFEV1)
Timeframe: From enrollment to the end of treatment at 12 weeks
Heart rate variability
Timeframe: From enrollment to the end of treatment at 12 weeks
Heart rate variability
Timeframe: From enrollment to the end of treatment at 12 weeks
Heart rate variability
Timeframe: From enrollment to the end of treatment at 12 weeks
Heart rate variability
Timeframe: From enrollment to the end of treatment at 12 weeks
Quality of Life(The short version of the World Health Organization Quality of Life ，WHOQOL-BREF)
Timeframe: From enrollment to the end of treatment at 12 weeks