About this trial
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.
Eligibility criteria
Qualifiers
PASC
above 20 y/o
Disqualifiers
Those who cannot cooperate
Severe schizophrenia
Trial design
Treatments tested in this trial
- QI-GONG and control
Treatment groups
Sponsors and collaborators
POCHIWU
Lead sponsor
National Taipei University of Nursing and Health Sciences
Sponsor institution