Actively Recruiting
Physiological and QoL Benefits of Qi-Gong in Post-acute Sequelae of Covid-19
Led by POCHIWU · Updated on 2025-03-17
80
Participants Needed
2
Research Sites
18 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Physiological and QoL Benefits of Qi-Gong in Post-acute Sequelae of Covid-19
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with post-acute sequelae of COVID-19 (PASC)
- Age above 20 years
You will not qualify if you...
- Unable to cooperate with study procedures
- Diagnosis of severe schizophrenia
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Renhe nursing home
New Taipei City, Taiwan
Actively Recruiting
2
Fuxi nursing home
Taipei, Taiwan
Actively Recruiting
Research Team
P
Po-Chi Wu
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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