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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03318289
Other study ID # 1602061
Secondary ID
Status Not yet recruiting
Phase N/A
First received October 9, 2017
Last updated October 18, 2017
Start date November 1, 2017
Est. completion date October 9, 2020

Study information

Verified date October 2017
Source The University of Hong Kong
Contact Shirley Fong, PhD
Phone 85228315260
Email smfong@hku.hk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Objectives: To evaluate the effects of a Ving Tsun (VT) reactive balance training programme on reactive balance control, muscle strength, balance confidence and falls in community-dwelling older adults.

Hypothesis: The VT group subjects will have improved post-training reactive balance control, muscle strength, balance confidence and fall incidence outcomes than the active controls.

Design and subjects: In this prospective, randomised, single-blinded controlled trial, approximately 114 healthy seniors (55-70 years old) will be randomly assigned to either the VT group (n~57) or control group (n~57). Interventions: Subjects in the VT group will receive VT reactive balance training (3 hours/week) for 3 months, whereas subjects in the control group will receive no VT training but will jog 3 hours/week during the intervention period.

Study instruments and outcomes: Primary outcome measures: reactive balance control, as indicated by lower extremity muscle activation onset latency; hip and ankle strategies and centre of pressure movements will be measured by electromyography, electrogoniometry and a force platform, respectively. Secondary outcome measures: knee muscle strength, balance confidence and fall history will be assessed by an isokinetic dynamometer, Activities-specific Balance Confidence Scale (Chinese) and interviews, respectively (pre-, post- and follow-up measurements).

Data analysis: Data will be analysed using repeated-measures analysis of (co)variance followed by post-hoc tests, as appropriate (alpha = 0.05).


Description:

Objectives:

To evaluate the effects of a Ving Tsun (VT) martial exercise programme on reactive balance control, lower limb muscle strength, balance confidence and falls in community-dwelling older adults.

Study design:

This will be a prospective, non-randomised and controlled intervention trial.

Subjects:

Approximately 40 healthy older adults will be recruited from elderly community centres by convenience sampling through poster advertising. Eligible subjects will be allocated to either the VT group (n ≈ 20) or control group (n ≈ 20).

Outcome measurements:

All subjects will be assessed before the intervention (baseline tests) and shortly after the 3-month intervention (post-tests). All subjects, regardless of group assignment, will undergo the following baseline tests and post-tests in random order.

Primary outcome measures Reactive balance control including lower extremity muscle activation onset latency and centre of pressure movement in standing.

Secondary outcome measures Lower extremity (knee) muscle strength, balance confidence and fall history.

Data analysis:

Data will be analysed using repeated-measures analysis of (co)variance followed by post-hoc tests, as appropriate (alpha = 0.05).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date October 9, 2020
Est. primary completion date October 9, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 55 Years to 70 Years
Eligibility Inclusion Criteria:

1. aged between 55 and 70 years,

2. able to ambulate independently,

3. an Abbreviated Mental Test (Hong Kong version) score > 7 and

4. able to follow commands and communicate with others.

Exclusion Criteria:

1. unstable medical condition (e.g. uncontrolled hypertension),

2. recent injury that may affect test performance,

3. history of fragility fractures,

4. significant musculoskeletal disorder (e.g. frozen shoulder),

5. sensorimotor disorder that may affect balance performance,

6. significant neurological disorder (e.g. stroke),

7. cardiopulmonary disease (e.g. chronic obstructive pulmonary disease),

8. cognitive disorders,

9. regular engagement in sports or martial arts training (e.g. Tai Chi) and

10. too frail to participate in VT intervention.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Ving Tsun
The VT training regimen is designed to improve reactive balance control, lower extremity muscle strength and balance confidence in the elderly. It comprises 9 VT sticking-hand drills that must be practised with a partner. Participants will be trained to respond rapidly to upper body perturbations and to maintain body balance. Those joined the VT training group will attend a one-hour supervised VT training session at an elderly community centre 2 times per week for 12 weeks.

Locations

Country Name City State
Hong Kong University of Hong Kong Hong Kong

Sponsors (1)

Lead Sponsor Collaborator
The University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary Lower extremity muscle activation onset latency Lower extremity muscle activation onset latency in response to postural preturbation will be measured using surface electromyography. 3 months
Primary Centre of pressure movement in standing Centre of pressure movement in standing will be measured using a force platform. 3 months
Secondary Knee maximum muscle strength Knee maximum muscle strength will be measured by an isokinetic dynamometer. 3 months
Secondary Balance confidence Balance confidence will be evaluated using the Activities-specific Balance Confidence Scale. Participants will be asked to rate on an 11-point scale ranging from 0 (no balance confident) to 100 (completely confident) for completing 16 daily activities while maintaining body balance. The mean of the total item score (0-100) will be used for analysis. Higher scores indicate better balance confidence. 3 months
Secondary Fall history The number of falls and fall related injuries will be obtained through interviews. 3 months
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