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Cost-utility and cost-effectiveness of a 8-wk whole-body vibration (WBV)-based intervention to improve balance and mobility among older adults with reduced mobility: a randomized controlled trial

Cost-utility and cost-effectiveness of a 8-wk WBV-based intervention to improve balance and mobility among older adults with reduced mobility: a randomized controlled trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12613000189729
Enrollment
50
Registered
2013-02-18
Start date
2013-03-04
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Objective: To test the feasibility, safety and effectiveness of a 8-wk whole body vibration (WBV) intervention on balance and mobility among older adults with reduced mobility in a nursing home context. Methods: Fifty older adults will be randomized 1:1 to an intervention group that, in addition to standard care, received a 8-wk WBV intervention, and a control group receiving only standard care . Outcomes, including balance, mobility and strenght or quality of life will be assessed after intervention

Interventions

Participants in the intervention group will have access to the usual care and will be asked not to change their nutritional or exercise habits during the 8-wk period. Participants in the intervention group will participate in a 8-week whole body vibration (WBV)-based program on an vertical platform consisting of three sessions per week with at least one day between sessions. Each exercise session will have a duration of 10 to 15 minutes with a frequency (load) of the vibrating platform of 20Hz

Participants in the intervention group will have access to the usual care and will be asked not to change their nutritional or exercise habits during the 8-wk period. Participants in the intervention group will participate in a 8-week whole body vibration (WBV)-based program on an vertical platform consisting of three sessions per week with at least one day between sessions. Each exercise session will have a duration of 10 to 15 minutes with a frequency (load) of the vibrating platform of 20Hz initially and progressing throughout the program up to 35 Hz and the amplitude will be of 4 mm in all sessions. Participants will stand on the platform in a semi-squat position in all exercises.

Sponsors

University of Seville
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
65 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

The inclusion criteria will be: Living in a nurse home and a level of exercise less than a150 min/week of moderate-intensity aerobic physical activity

Exclusion criteria

Potential participants were excluded if they had a baseline value for fasting blood glucose > 250 mg/dl or HbA1c > 10%, diagnosed cardiovascular or mental disease, a diabetes-related complication including nephropathy, or retinopathy unrepaired hernia, or any other functional impairment that would preclude safe participation in a WBV-based training program

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026