Ving Tsun Martial Exercise for Older Adults

Exercise is Medicine and Community Wellness - A Ving Tsun Martial Exercise Programme for Community-dwelling Older Adults

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).

Study Overview

• Status: Unknown
• Conditions: Old Age; Atrophy
• Intervention / Treatment: Behavioral: Ving Tsun

Detailed 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).

• Study Type: Interventional
• Enrollment (Anticipated): 40
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Hong Kong
  • Hong Kong, Hong Kong
    • University of Hong Kong

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 51 years to 66 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

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 Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Ving Tsun (VT) group; Participants in the VT group will receive VT exercise intervention for 12 weeks.	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.
No Intervention: Control group; No intervention but can continue daily activities.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
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
Centre of pressure movement in standing	Centre of pressure movement in standing will be measured using a force platform.	3 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Knee maximum muscle strength	Knee maximum muscle strength will be measured by an isokinetic dynamometer.	3 months
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
Fall history	The number of falls and fall related injuries will be obtained through interviews.	3 months

Collaborators and Investigators

• Sponsor: The University of Hong Kong

Study record dates

Study Major Dates

• Study Start (Anticipated): November 1, 2017
• Primary Completion (Anticipated): October 9, 2020
• Study Completion (Anticipated): October 9, 2020

Study Registration Dates

• First Submitted: October 9, 2017
• First Submitted That Met QC Criteria: October 18, 2017
• First Posted (Actual): October 23, 2017

Study Record Updates

• Last Update Posted (Actual): October 23, 2017
• Last Update Submitted That Met QC Criteria: October 18, 2017
• Last Verified: October 1, 2017

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathological Conditions, Anatomical; Atrophy
• Other Study ID Numbers: 1602061

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No