Understanding the Psychological Benefits and Neurophysiological Mechanisms of Qigong in Older Adults
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Qigong (Baduanjin), Mindfulness-based intervention, Physical exercise.
- Who it may be relevant to
- Registry conditions: Qigong. Basic parameters: from 60 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Hong Kong
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
One goal of the study is to evaluate the efficacy of qigong to alleviate depressive symptoms and enhance cognitive function in comparison to mindfulness-based intervention, physical exercise, and waitlist control. The other goal is to explore the changes in neurobiological markers that may explain the qigong-related effects on depressive symptoms and cognitive function. The main research questions are: * Is the 12-week qigong training more effective than mindfulness-based intervention, physical exercise, and waitlist control to alleviate depressive symptoms? * Is the 12-week qigong training more effective than mindfulness-based intervention, physical exercise, and waitlist control to enhance cognitive function? Participants are older adults aged 60 or above. They were randomly assigned to qigong training, mindfulness training, physical exercise training, or wait-list which all last for 12 weeks. Their changes before and after the 12-week period in depressive symptoms, neurobiological markers, and cognitive functions are assessed.
Interventions
- Behavioral Qigong (Baduanjin)
Participants will receive 24 sessions of Baduanjin training over 12 weeks (2 sessions per week). Each session will last for 60 minutes. Baduanjin consists of eight forms of gentle movements, and it takes about 10 to 15 minutes to complete a full cycle. Participants will learn to practice each form gradually over the first 12 sessions. In the remaining 12 sessions, the participants will go through all the movements 2-3 times, with guided practice on rhythmic breathing and mind regulation (attenti - Behavioral Mindfulness-based intervention
Participants will receive mindfulness-based intervention with the same duration and frequency as qigong group. The intervention incorporates psychoeducation on mindfulness and stress management and group-based mindfulness practice about breathing, awareness of body sensations, thoughts, stretching, and walking. All the mindfulness practices are based on publicly accessible audio recordings. The training will be delivered by an instructor after training by the project team. - Behavioral Physical exercise
Participants of the physical exercise group will receive training of a series of low-to-moderate intensity physical activities for the same duration and frequency as qigong group. The physical activities include stretching, flexibility exercise, balance exercise, and aerobic exercise. The training will be delivered by an instructor after training by the project team.
Primary outcome measures
- Depressive symptoms [Time frame: Baseline and post-intervention (12 weeks after baseline)]
- Global cognitive function [Time frame: Baseline and post-intervention (12 weeks after baseline)]
Secondary outcome measures (10)
- Serum adiponectin [Time frame: Baseline and post-intervention (12 weeks after baseline)]
- Serum BDNF [Time frame: Baseline and post-intervention (12 weeks after baseline)]
- Salivary cortisol [Time frame: Baseline and post-intervention (12 weeks after baseline)]
- Attention [Time frame: Baseline and post-intervention (12 weeks after baseline)]
- Inhibitory control [Time frame: Baseline and post-intervention (12 weeks after baseline)]
- Working memory [Time frame: Baseline and post-intervention (12 weeks after baseline)]
- ERP N2 amplitude [Time frame: Baseline and post-intervention (12 weeks after baseline)]
- ERP P3 amplitude [Time frame: Baseline and post-intervention (12 weeks after baseline)]
- Hand grip strength [Time frame: Baseline and post-intervention (12 weeks after baseline)]
- Affect [Time frame: Baseline and post-intervention (12 weeks after baseline)]
Eligibility criteria
Inclusion criteria
- 60 years or older;
- With mild or severer levels of depressive symptoms as indicated by the Geriatric Depression Scale (GDS-8) scores of 5 or above, or Depression Anxiety and Stress Scale-21 (DASS-21) depression subscale scores of 4 or above
- Self-identified as physically stable and without life-threatening diseases.
- Be able to communicate in Cantonese or Mandarin.
Exclusion criteria
- Have a history of practicing or receiving training of any form of mind-body or regular exercises (including tai chi, yoga, and qigong, or regular physical activity > 3 times/week) during the month prior to intervention
- Have changed medications or the dose of medications prescribed for their health condition in the one month prior to study enrollment
- Have severe cognitive or language impairment based on the assessment with Montreal Cognitive Assessment (MoCA)
- Taking medication or undergoing electroconvulsive therapy, psychotherapy, or psychoeducation for a psychological or psychiatric condition
- Unable to demonstrate satisfactory standing balance
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Supportive care
Study locations
Hong Kong · 1 center
- Hong Kong Polytechnic University, Department of Rehabilitation Sciences — Kowloon
Identifiers
NCT: NCT06952166 · 15104721-2