Jouf University
Fahad Alanazi
This is a double-blind, randomized controlled trial comparing WBV therapy with a placebo intervention and standard care. A total of 150 participants will be recruited and investigated from Prince Mutib Hospital. Participants will be randomly allocated to one of three groups: WBV therapy, placebo (non-vibrating platform), or control (standard care). The study duration will be 12 weeks, with assessments conducted at baseline, post-intervention (12 weeks), and at a 6-month follow-up. Protocol Parameters Summary * Session Frequency: 3 times per week. * Session Duration: 25 minutes per session. * Vibration Frequency: 30 Hz. * Amplitude: 1-2 mm. * Program Duration: 12 weeks.
Cognitive Impairment
Balance
Quality of Life
WBV Therapy Group
Placebo Group:
Control
NA
Study Type : | INTERVENTIONAL |
Estimated Enrollment : | 180 participants |
Masking : | DOUBLE |
Primary Purpose : | TREATMENT |
Official Title : | Effects of Whole Body Vibration Therapy on Cognitive Function, Balance, and Quality of Life in Older Adults With Mild Cognitive Impairment: A Randomized, Double-Blind, Placebo-Controlled Trial |
Actual Study Start Date : | 2025-06-01 |
Estimated Primary Completion Date : | 2025-12-30 |
Estimated Study Completion Date : | 2025-12-30 |
Information not available for Arms and Intervention/treatment
Ages Eligible for Study: | 60 Years |
Sexes Eligible for Study: | ALL |
Accepts Healthy Volunteers: |
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