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Effect of Qigong on Balance, Fall Efficacy, Wellbeing of People With Stroke in Hong Kong

Effect of Qigong on Balance, Fall Efficacy, Physical Functions and Psychological Wellbeing of People With Stroke in Hong Kong: A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02999464
Enrollment
58
Registered
2016-12-21
Start date
2016-07-31
Completion date
2017-07-31
Last updated
2017-01-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

stroke, qigong, randomized controlled trial, body-mind exercise, balance, quality of life, wellbeing

Brief summary

The purpose of this study is to compare the effects of qigong practice with fitness exercise on balance, fall-efficacy, physical functions, psychological wellbeing and quality of life of stroke survivors.

Detailed description

Participants: A total of 58 stroke survivors 3 months after the current stroke will be recruited. Methodology: An assessor-blinded, randomized controlled trial will be conducted. Stroke survivors will be included in the study if they meet the inclusion criteria. Selected patients will be randomly allocated into either the experimental group or the control group. Participants allocated in the experimental group will receive qigong training while this qigong training will be replaced by a home fitness exercise in the control group. The experimental and control groups will be required to practice a total of 50 minutes of qigong and fitness training 3 times per week and for 16 weeks respectively. The main outcome measure is balance capacity with Mini-BESTest. The secondary outcomes are fall efficacy, number of falls, postural stability and control, depression, physical functions and quality of life. Assessments will be done at baseline, 8 weeks and 16 weeks follow-ups by blinded assessors. Data analysis: The results will be analyzed using two-way repeated measures analysis of variance with Statistical Package for Social Science version 21.0. Alpha will be set at 0.05.

Interventions

OTHERQigong

The experimental group will be required to practice a total of 50 minutes of qigong training 3 times per week and for 16 weeks

OTHERFitness exercise

Active control group will be required to practice a total of 50 minutes of fitness training 3 times per week and for 16 weeks

Sponsors

The Hong Kong Polytechnic University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Diagnosis of stroke and 3 months after the onset * First episode of stroke or recurrent of stroke * Able to stand for more than 15 minutes * Able to take anterioposterior and lateral step without assistance or aid * Medically stable * Sufficient cognition to follow commands Abbreviated Mental Test (AMT) score ≥7

Exclusion criteria

* Vital signs unstable * History or evidence of other neurological deficits other than stroke such as multiple sclerosis * Severe primary diseases of the cardiovascular system, liver, kidney or hematopoietic system * Experience in qigong practice

Design outcomes

Primary

MeasureTime frameDescription
Mini-BESTest.Baseline, 8th week and 16th week after interventionChange from baseline balance capacity at 8 weeks and 16 weeks

Secondary

MeasureTime frameDescription
Number of fallsBaseline, 8th week and 16th week after intervention
Limit of Stability by using Balance MasterBaseline, 8th week and 16th week after interventionChange from baseline postural stability at 8 weeks and 16 weeks
Geriatric Depression ScaleBaseline, 8th week and 16th week after intervention
Five Times Sit to Stand TestBaseline, 8th week and 16th week after interventionLower extremity strength
Fall Efficacy Scale - InternationalBaseline, 8th week and 16th week after interventionChange from baseline fall efficacy of the subject at 8 weeks and 16 weeks
Modified Barthel IndexBaseline, 8th week and 16th week after interventionActivities of daily living function
Stroke-Specific Quality of Life ScaleBaseline, 8th week and 16th week after intervention
Sensory Organization Test by using Balance MasterBaseline, 8th week and 16th week after interventionChange from baseline postural control at 8 weeks and 16 weeks
Timed Up and Go TestBaseline, 8th week and 16th week after interventionChange from baseline gait speed at 8 weeks and 16 weeks

Countries

Hong Kong

Contacts

Primary ContactShuk-man YUEN, MPhil
mandyyuensm@yahoo.com.hk852-9736-3529
Backup ContactYiu-chung PANG, PhD
Marco.Pang@polyu.edu.hk852-2766-7156

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026