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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01735682
Other study ID # HSEARS20120730001
Secondary ID
Status Recruiting
Phase N/A
First received November 20, 2012
Last updated May 29, 2014
Start date November 2012
Est. completion date October 2015

Study information

Verified date May 2014
Source The Hong Kong Polytechnic University
Contact Philip Chan, MSc
Phone 852-9851-1382
Email cfl083@gmail.com
Is FDA regulated No
Health authority Hong Kong: Research Office, The Hong Kong Polytechnic University
Study type Interventional

Clinical Trial Summary

It is hypothesized that whole body vibration exercise group will have significantly more improvement in physical functioning and reduction in fall incidence among institutionalized elderly, compared with conventional exercise group and control group.


Recruitment information / eligibility

Status Recruiting
Enrollment 68
Est. completion date October 2015
Est. primary completion date April 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 65 Years and older
Eligibility Inclusion Criteria:

- Functional Ambulation Category 1 to 4

- able to understand simple verbal commands

- able to tolerate intermittent physical activity for at least 45 minutes

- able to perform knee flexion >45 degree

- able to stand with or without support for 1 minute or more

Exclusion Criteria:

- peripheral vascular disease

- any symptoms associated with vestibular disorder

- any contraindications to exercise (e.g. unstable angina)

- any serious illnesses that preclude participation (e.g. cancer)

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Whole body vibration
The vibration frequency and amplitude used will be 30-40 Hz and 1mm, respectively. The total exposure to the vibration stimulation is 4 minutes.
Behavioral:
Conventional exercise
The conventional exercise training involves upper limb and lower limb strengthening exercises using sandbags.
Control
The control treatment involves exercises of the upper limbs.

Locations

Country Name City State
Hong Kong Shatin Hospital Shatin New Territories

Sponsors (2)

Lead Sponsor Collaborator
The Hong Kong Polytechnic University Shatin Hospital, Hong Kong

Country where clinical trial is conducted

Hong Kong, 

References & Publications (2)

Bautmans I, Van Hees E, Lemper JC, Mets T. The feasibility of Whole Body Vibration in institutionalised elderly persons and its influence on muscle performance, balance and mobility: a randomised controlled trial [ISRCTN62535013]. BMC Geriatr. 2005 Dec 22;5:17. — View Citation

Bruyere O, Wuidart MA, Di Palma E, Gourlay M, Ethgen O, Richy F, Reginster JY. Controlled whole body vibration to decrease fall risk and improve health-related quality of life of nursing home residents. Arch Phys Med Rehabil. 2005 Feb;86(2):303-7. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Timed-Up-and-Go test It is a measure of functional mobility week 0 No
Primary Timed-up-and-go test week 8 No
Secondary Berg balance scale week 0 No
Secondary Berg balance scale week 8 No
Secondary leg extension strength week 0 No
Secondary leg extension strength week 8 No
Secondary shoulder abduction strength week 0 No
Secondary shoulder abduction strength week 8 No
Secondary elbow flexion strength week 0 No
Secondary elbow flexion strength week 8 No
Secondary six minute walk test week 0 No
Secondary six minute walk test week 8 No
Secondary Activities-specific balance confidence scale week 0 No
Secondary Activities-specific balance confidence scale week 8 No
Secondary Quick DASH A measure of upper limb function week 0 No
Secondary Quick DASH week 8 No
Secondary Physiological Profile Assessment: short form week 0 No
Secondary Physiological Profile Assessment: short form week 8 No
Secondary falls incidence Daily from week 0 to 12 months after termination of treatment/control period No
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