Skip to main content
Clinical Trials/NCT02999464
NCT02999464UnknownNot Applicable

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

The Hong Kong Polytechnic University1 site in 1 country58 target enrollmentStarted: July 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
58
Locations
1
Primary Endpoint
Mini-BESTest.

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Sex
All
Accepts 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

Arms & Interventions

Qigong

Experimental

Experimental group will receive a total of 50 minutes of qigong training 3 times per week and for 16 weeks.

Intervention: Qigong (Other)

Fitness Exercise

Active Comparator

Fitness exercise group will receive home fitness exercise 3 times per week and for 16 weeks.

Intervention: Fitness exercise (Other)

Outcomes

Primary Outcomes

Mini-BESTest.

Time Frame: Baseline, 8th week and 16th week after intervention

Change from baseline balance capacity at 8 weeks and 16 weeks

Secondary Outcomes

  • Fall Efficacy Scale - International(Baseline, 8th week and 16th week after intervention)
  • Sensory Organization Test by using Balance Master(Baseline, 8th week and 16th week after intervention)
  • Number of falls(Baseline, 8th week and 16th week after intervention)
  • Limit of Stability by using Balance Master(Baseline, 8th week and 16th week after intervention)
  • Geriatric Depression Scale(Baseline, 8th week and 16th week after intervention)
  • Five Times Sit to Stand Test(Baseline, 8th week and 16th week after intervention)
  • Timed Up and Go Test(Baseline, 8th week and 16th week after intervention)
  • Modified Barthel Index(Baseline, 8th week and 16th week after intervention)
  • Stroke-Specific Quality of Life Scale(Baseline, 8th week and 16th week after intervention)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Yuen Shuk Man

Principal investigator

The Hong Kong Polytechnic University

Study Sites (1)

Loading locations...

Similar Trials