Actively Recruiting
Developing an Integrated Mindfulness-based Health Qigong Intervention for COVID-19 Survivors and Caregivers to Improve Physical and Psychological Wellness
Led by The Hong Kong Polytechnic University · Updated on 2024-01-08
600
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the effects of an integrated intervention combining Health Qigong, a traditional Chinese martial art focusing on body movement and mind status, with mindfulness-based interventions (MBIs) to improve mental and physical wellbeing. This program targets COVID-19 survivors, their caregivers including healthcare providers and family members, as well as the general public affected by COVID-19-related depression, anxiety, and stigma. The study aims to assess if this combined approach can reduce fear, anxiety, and stigma by enhancing stress, cognitive, and mood coping strategies. Participants are randomly assigned to either the treatment group or a control group. Those in the treatment group begin with an in-person session to learn essential mindfulness skills, basic Qigong movements, and how to use a resource package. They then attend eight bi-weekly online mindfulness sessions via a mobile app, each lasting about two hours. After these sessions, participants practice Qigong for 30 minutes a day, five days a week, for eight weeks, supported by follow-up coaching through the app. Booster sessions occur every three months after the initial 16-week intervention, with follow-up assessments every six months for two years. During the study, participants will be monitored through follow-up assessments that evaluate psychological wellbeing over two years, including the Multidimensional Assessment of Interoceptive Awareness (MAIA). The study involves regular online sessions, daily practice, and booster sessions to support adherence. Researchers will track mental and physical health improvements and gather data on the long-term effects of the integrated intervention to support rehabilitation and wellbeing in the community.
CONDITIONS
Brief Title
Integrated Mindfulness-based Health Qigong Intervention for COVID-19 Survivors and Caregivers
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or above who are COVID-19 survivors, both symptomatic and asymptomatic, and clinically recovered
- Caregivers of COVID-19 patients, including family members or medical professionals aged 18 years or above in contact with diagnosed patients
- General healthy public aged 18 years or above
You will not qualify if you...
- Individuals with severe and/or chronic conditions preventing Qigong or mindfulness practice (e.g., acute exacerbation of dyspnoea, severe cardiopulmonary disease)
- People with severe psychiatric disorders
- People who have regular psychiatric follow-ups
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 16 weeks
Participants in the intervention group receive an initial face-to-face session introducing mindfulness, basic Qigong movements, and resource use. This is followed by 8 bi-weekly online mindfulness sessions via the Mobile App, then 8 weeks of Qigong practice for 30 minutes per day, five days a week, with follow-up coaching sessions via the Mobile App.
1 initial in-person session and 8 bi-weekly online sessions, followed by ongoing daily practice and follow-up sessions
Duration - 2 years
After completing the 16-week intervention, participants receive booster sessions every 3 months to revise the interventions. Follow-up assessments are conducted every 6 months for 2 years to monitor physical and psychological wellness.
Booster sessions every 3 months and follow-up assessments every 6 months
Trial Site Locations
Total: 1 location
1
Princess Margaret Hospital
Hong Kong, Hong Kong, 852
Actively Recruiting
Research Team
T
Travis,Tsz-kwun Law, Mr
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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