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Clinical Trials/NCT03591211
NCT03591211
Completed
Not Applicable

Bio-psycho-social Pathways Underlying the Effects of Qigong Among Comorbid Depressed Elderly With Chronic Conditions

The Hong Kong Polytechnic University1 site in 1 country35 target enrollmentAugust 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Disease
Sponsor
The Hong Kong Polytechnic University
Enrollment
35
Locations
1
Primary Endpoint
Patient Health Questionnaire (PHQ)
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Depression and chronic medical conditions are common in older adults. Qigong is increasingly documented to have anti-depressive effects for older adults. Nevertheless, the scientific concepts behind qigong remain a mystery. To fill the knowledge gap, the neurobiological mechanism of the effects of qigong was explored. In addition, the benefits of qigong on subjective well-being, functional independence, sleep quality, mobility, and muscle strength were also tested. After random assignment, intervention group (n = 14) went through individual qigong exercise twice a week and for 12 weeks,whereas control group (n = 16) was involved in cognitive training activities with mobilization elements. The psychosocial, physical, and neurobiological outcomes of the two groups were compared.

Registry
clinicaltrials.gov
Start Date
August 1, 2017
End Date
February 28, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

TSANG Hector Wing-Hong

Professor and Head of Department of Rehabilitation Sciences

The Hong Kong Polytechnic University

Eligibility Criteria

Inclusion Criteria

  • aged 60 or above
  • have been suffering from chronic medical conditions for more than one year
  • have depressive symptoms as indicated by Geriatric Depression Scale (GDS ≥ 6)

Exclusion Criteria

  • have practiced or received training of any form of mind-body exercises (including tai chi, yoga, and qigong) during the 6 months prior to intervention.
  • have changed medication or the dosage prior to or during intervention
  • have obvious cognitive and language impairment or score less than 20 in Mini-Mental State Examination (MMSE)
  • undergo electroconvulsive therapy, psychotherapy, or psychoeducation
  • cannot demonstrate satisfactory sitting balance

Outcomes

Primary Outcomes

Patient Health Questionnaire (PHQ)

Time Frame: the change from baseline to the completion of intervention (12 weeks later)

Patient Health Questionnaire (PHQ) is used to assess the experience of depressive symptoms. The frequency of each symptom was indicated based on a 4-point scale (0 = never; 3 = almost every day). A total score ranged from 0 to 27 can be derived, with higher score indicating severer depressive symptoms.

Secondary Outcomes

  • Brain Deprived Neurotrophic Factor (BDNF) Level(baseline and 12 weeks after baseline)
  • Depression Anxiety Stress Scale (DASS-21)(baseline, 12 weeks after baseline, and 16 weeks after baseline)
  • Personal Well-Being Index (PWI)(baseline, 12 weeks after baseline, and 16 weeks after baseline)
  • Functional Independence Measure (FIM)(baseline, 12 weeks after baseline, and 16 weeks after baseline)
  • Timed up and Go Test (TUG)(baseline, 12 weeks after baseline, and 16 weeks after baseline)
  • Handgrip Strength(baseline, 12 weeks after baseline, and 16 weeks after baseline)
  • Salivary Cortisol Level(baseline and 12 weeks after baseline)
  • Serotonin 5-HT Level(baseline and 12 weeks after baseline)
  • Pittsburgh Sleep Quality Index (PSQI)(baseline, 12 weeks after baseline, and 16 weeks after baseline)

Study Sites (1)

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