The Effect of Whole-body Vibration Training
1 other identifier
interventional
42
0 countries
N/A
Brief Summary
The whole-body vibration programme employed in this study partly improved the biomarkers and health beliefs of the prefrail community-dwelling older adults.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2016
Shorter than P25 for not_applicable
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
Study Start
First participant enrolled
March 18, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 25, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
June 25, 2016
CompletedFirst Submitted
Initial submission to the registry
November 6, 2019
CompletedFirst Posted
Study publicly available on registry
February 18, 2020
CompletedFebruary 18, 2020
February 1, 2020
3 months
November 6, 2019
February 17, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (6)
Pretest and posttest results of the experimental and control groups for Grip strength
Comparison of grip strength before and after 12 weeks of training
Change from baseline at 12 weeks (The experimental group participated training that was conducted 3 times per week, with 5-min continuous vibration)
Pretest and posttest results of the experimental and control groups for 15-foot walk test speed
Comparison of 15-foot walk test speed before and after 12 weeks of training
Change from baseline at 12 weeks (The experimental group participated training that was conducted 3 times per week, with 5-min continuous vibration)
Pretest and posttest results of the experimental and control groups for One-leg standing test using the dominant leg with the eyes open
Comparison of One-leg standing test with the eyes open before and after 12 weeks of training
Change from baseline at 12 weeks (The experimental group participated training that was conducted 3 times per week, with 5-min continuous vibration)
Pretest and posttest results of the experimental and control groups for Thirty-second chair stand test
Comparison of Thirty-second chair stand test before and after 12 weeks of training
Change from baseline at 12 weeks (The experimental group participated training that was conducted 3 times per week, with 5-min continuous vibration)
Pretest and posttest results of the experimental and control groups for Two-minute step test
Comparison of Two-minute step test before and after 12 weeks of training
Change from baseline at 12 weeks (The experimental group participated training that was conducted 3 times per week, with 5-min continuous vibration)
Pretest and posttest results of the experimental and control groups for Health beliefs
Comparison of health beliefs before and after 12 weeks
The twelfth week
Secondary Outcomes (2)
Summary of posttest ANCOVA of the experimental and control groups for biomarkers
The twelfth week
Summary of posttest ANCOVA of the experimental and control groups for health beliefs
The twelfth week
Study Arms (1)
whole-body vibration training
EXPERIMENTALa 12-week whole-body vibration training that conducted 3 times per week, with 5-min continuous vibration at 12-Hz frequency and 3-mm amplitude each time.
Interventions
The experimental group participated in a 12-week whole-body vibration training that was conducted 3 times per week, with 5-min continuous vibration at 12-Hz frequency and 3-mm amplitude each time. The control group were provided home DVDs on resistance exercise and manuals for preventing frailty
Eligibility Criteria
You may qualify if:
- Age of 65 years or older and living in a community
- Full consciousness and able to communicate verbally
- No severe cognitive disorder
You may not qualify if:
- Impaired mobility after recent surgery
- Major illness such as cancer
- Severe hearing impairment and inability to fully understand and follow instructions
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
November 6, 2019
First Posted
February 18, 2020
Study Start
March 18, 2016
Primary Completion
June 25, 2016
Study Completion
June 25, 2016
Last Updated
February 18, 2020
Record last verified: 2020-02