NCT03318289

Brief 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).

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Nov 2017

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 9, 2017

Completed
14 days until next milestone

First Posted

Study publicly available on registry

October 23, 2017

Completed
9 days until next milestone

Study Start

First participant enrolled

November 1, 2017

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 9, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 9, 2020

Completed
Last Updated

October 23, 2017

Status Verified

October 1, 2017

Enrollment Period

2.9 years

First QC Date

October 9, 2017

Last Update Submit

October 18, 2017

Conditions

Outcome Measures

Primary Outcomes (2)

  • 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 Outcomes (3)

  • Knee maximum muscle strength

    3 months

  • Balance confidence

    3 months

  • Fall history

    3 months

Study Arms (2)

Ving Tsun (VT) group

EXPERIMENTAL

Participants in the VT group will receive VT exercise intervention for 12 weeks.

Behavioral: Ving Tsun

Control group

NO INTERVENTION

No intervention but can continue daily activities.

Interventions

Ving TsunBEHAVIORAL

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.

Ving Tsun (VT) group

Eligibility Criteria

Age55 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • aged between 55 and 70 years,
  • able to ambulate independently,
  • an Abbreviated Mental Test (Hong Kong version) score \> 7 and
  • able to follow commands and communicate with others.

You may not qualify if:

  • unstable medical condition (e.g. uncontrolled hypertension),
  • recent injury that may affect test performance,
  • history of fragility fractures,
  • significant musculoskeletal disorder (e.g. frozen shoulder),
  • sensorimotor disorder that may affect balance performance,
  • significant neurological disorder (e.g. stroke),
  • cardiopulmonary disease (e.g. chronic obstructive pulmonary disease),
  • cognitive disorders,
  • regular engagement in sports or martial arts training (e.g. Tai Chi) and
  • too frail to participate in VT intervention.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Hong Kong

Hong Kong, Hong Kong

Location

Related Publications (1)

  • Fong SSM, Chung LMY, Yam TTT, Chung JWY, Bae YH, Gao Y, Chan JSM, Wang HK. Effects of Ving Tsun sticking-hand training on lower limb sensorimotor performance among community-dwelling middle-aged and older adults: a randomized controlled trial. Trials. 2023 Feb 25;24(1):143. doi: 10.1186/s13063-023-07133-2.

MeSH Terms

Conditions

Atrophy

Condition Hierarchy (Ancestors)

Pathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Study Officials

  • Shirley Fong, PhD

    The University of Hong Kong

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Shirley Fong, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

October 9, 2017

First Posted

October 23, 2017

Study Start

November 1, 2017

Primary Completion

October 9, 2020

Study Completion

October 9, 2020

Last Updated

October 23, 2017

Record last verified: 2017-10

Data Sharing

IPD Sharing
Will not share

Locations