Integrated Mindfulness-based Health Qigong Intervention for COVID-19 Survivors and Caregivers

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorThe Hong Kong Polytechnic University

About this trial

COVID-19-related depression, anxiety, and stigma are expected to have short-term and long-term adverse impacts on mental health, help seeking and preventive behaviours in affected individuals, including care providers and the general population. Health qigong (HQ), a form of traditional Chinese martial arts with emphasis placed on the body movement and status of mind, has been demonstrated to enhance both physical and mental health. Mindfulness-based interventions (MBIs), another mind-body treatment, have become increasingly popular for treating a number of health problems. This study proposes an integrated intervention that combines the effects of HQ and MBIs (iMBHQ) to improve the mental wellbeing of COVID-19 survivors, caregivers including healthcare providers and family members as well as the general public in the community.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

COVID-19 survivors: people aged 18 years or above who were infected by COVID-19 (both symptomatic and asymptomatic) and clinically recovered

Caregivers of COVID-19 patients, including family members or medical professionals who have contacts with patients diagnosed COVID-19 aged 18 years or above

General healthy public aged 18 years or above

Disqualifiers

people diagnosed severe and/or chronic conditions that prevent the practice of Qigong (e.g., acute exacerbation of dyspnoea, severe cardiopulmonary disease) or mindfulness intervention,

people with severe psychiatric disorder

people who have regular psychiatric follow-ups

Trial design

Design model

Parallel

Treatments tested in this trial

  • Mindfulness-based Health Qigong Intervention

    Other intervention

    Participants are introduced the practice of the most essential skills, particularly mindfulness, the basic movements of Qigong and the use of the resources package. Following the initial session, participants will kick off 8 bi-weekly online sessions of Mindfulness-based interventions approximately two hours each via the Mobile App. Afterwards, participants will be asked to practice Qigong for 30 minutes per day with five days weekly for another 8 weeks. Follow-up sessions will be conducted by an experienced coach via the Mobile App. After the first 16-week intervention, booster sessions will be provided every 3 months to revise the interventions and follow-up assessments will be completed every 6 months for 2 years.

Treatment groups

600 Participants
are divided into 2 treatment groups
Group A: Intervention groupExperimental treatment 1 intervention
Group B: Control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Psychological wellbeing

Depression, Anxiety and Stress Scale (DASS-12)

Time frame
2 years

Secondary outcomes

1

Multidimensional Assessment of Interoceptive Awareness (MAIA)

12-item Short Form healthy survey (SF-12); Rumination Reflection Questionnaire (RRQ); Hyperarousal Scale COVID-19 Fear Scale; Stigma: Perceived stigma and Self-stigma Scale; Attitudes toward rapid testing and vaccine scale

Time frame
2 years

Other outcomes

Sponsors and contacts

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