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Unpacking the "Mind" and "Body" Pathways of the Antidepressant Effect of Qigong in Older Adults: A Pilot Study

T

The Hong Kong Polytechnic University

Status

Completed

Conditions

Qigong

Treatments

Behavioral: Qigong
Behavioral: Mindfulness-based training
Behavioral: Low-to-moderate intensity physical exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT06804408
15104721-1

Details and patient eligibility

About

The goals of the study are to explore the neurobiological mechanisms and cognitive benefits of qigong in older adults. The main research questions are:

  • Does 12-week qigong training lead to significant enhancement in serum adiponectin, serum BDNF and significant reduction in salivary cortisol?
  • Does 12-week qigong training bring significant improvement in global 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.

Enrollment

106 patients

Sex

All

Ages

60+ years old

Volunteers

Accepts Healthy Volunteers

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.

Exclusion criteria

  • With 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 study enrollment
  • Having changed medications or the dose of medications prescribed for their health condition in the month prior to study enrollment
  • With severe cognitive or language impairment as defined as a score of less than 21 on Montreal Cognitive Assessment (MoCA-5min)
  • Undergoing electroconvulsive therapy, psychotherapy, or psychoeducation for a psychological or psychiatric condition
  • Unable to demonstrate satisfactory standing balance.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

106 participants in 4 patient groups

Qigong
Experimental group
Description:
12-week training of Baduanjin (or named Eight-Section Brocades), with two sessions per week. Each session lasts for 60 min.
Treatment:
Behavioral: Qigong
Mindfulness-based Training
Active Comparator group
Description:
12-week training of mindfulness-based breathing, walking, and stretching practices, with two sessions per week. Each session lasts for 60 min.
Treatment:
Behavioral: Mindfulness-based training
Low-to-moderate Intensity Physical Exercise
Active Comparator group
Description:
12-week training of stretching, flexibility exercise, and balance exercise, with two sessions per week. Each session lasts for 60 min.
Treatment:
Behavioral: Low-to-moderate intensity physical exercise
Waitlist
No Intervention group
Description:
No training while the other three group are receiving training. Participants of this group are allowed to have Qigong, Mindfulness-based Training, or Low-to-moderate Intensity Physical Exercise after they complete all the assessments.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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