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Whole Body Vibration Exercise for Elderly With Cognitive Impairments

T

The Hong Kong Polytechnic University

Status

Unknown

Conditions

Dementia

Treatments

Device: Whole body vibration exercise
Behavioral: Conventional exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT01734083
HSEARS20120929006

Details and patient eligibility

About

The whole body vibration exercise group will have significantly more improvement in mobility, muscle strength, balance, balance confidence, and cognitive function with a lower fall rate than the control group.

Enrollment

66 estimated patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • a diagnosis of mild or moderate dementia, with a Clinical Dementia Rating (CDR) of 1 to 2, and a Cantonese Mini-mental State Examination (CMMSE) score at 10 or above but below the local cutoff for dementia (18-22, depending on education level)
  • able to stand for at least 1 minute with or without hand support
  • living in the community
  • having an informed consent (from the primary caregiver)

Exclusion criteria

  • significant musculoskeletal conditions (e.g. amputations)
  • metal implants in the lower extremity
  • recent fracture in the lower extremity
  • vestibular disorders
  • peripheral vascular disease
  • other serious illnesses or contraindications to exercise.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

66 participants in 2 patient groups

Whole body vibration exercise
Experimental group
Description:
The experimental group will receive 2 sessions of whole body vibration exercise training and conventional exercise per week for a period of 9 weeks. The total duration of vibration exposure per session will range from 4 to 6 minutes. The vibration frequency and amplitude used will be 30 Hz and 1 mm, respectively.
Treatment:
Device: Whole body vibration exercise
Behavioral: Conventional exercise
Conventional exercise
Active Comparator group
Description:
This group will receive 2 sessions of conventional exercise training per week for a period of 9 weeks.
Treatment:
Behavioral: Conventional exercise

Trial contacts and locations

1

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Central trial contact

Marco Pang, PhD

Data sourced from clinicaltrials.gov

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