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Whole Body Vibration in Middle Aged Men

Effects of Whole-Body Vibration on Bone Mineral Density, Hand Grip Strength, and Vitamin D Levels in Middle-Aged Men: a Preliminary Clinical Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06644469
Enrollment
34
Registered
2024-10-16
Start date
2024-10-15
Completion date
2024-12-15
Last updated
2024-10-18

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

Conditions

Bone Density, Muscle Weakness

Keywords

Pilot Study, Bone Density, Vibration Therapy, Vitamin D, Muscle Strength

Brief summary

This study aims of this clinical trial is to evaluate the effect of an 8-week Whole Body Vibration (WBV) intervention on Bone Mineral Density (BMD), hand grip strength, and vitamin D levels in middle-aged men. Findings from this study will contribute to understanding whether WBV is a viable alternative to conventional exercise, especially for those with limitations in physical activity. Study Objectives: • Primary Objective: To assess the effectiveness of an 8-week WBV intervention in improving BMD, hand grip strength, and vitamin D levels compared to a placebo intervention.

Interventions

DEVICEDynatronics VF5 Model vibration platform

The Dynatronics VF5 Model vibration platform is a specialized therapeutic device designed for rehabilitation and wellness applications. Utilizing advanced vibration technology, it provides whole-body vibration therapy that can enhance muscle strength, improve flexibility, and promote overall physical well-being. The platform features adjustable frequency and amplitude settings, allowing customization based on individual needs. Its user-friendly interface and robust, durable design make it suitable for both clinical and mobile therapy settings. Additionally, the compact and portable nature of the VF5 facilitates easy storage and transport, while safety features such as non-slip surfaces ensure user protection.

DEVICEPlacebo Dynatronics VF5 Model vibration platform

Placebo intensity with vertical vibration of 0.2 mm

Sponsors

Jouf University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Masking description

The participants will be unaware of whether they are receiving vibration therapy, and the individual performing the assessment will be different from the one administering the treatment

Eligibility

Sex/Gender
MALE
Age
50 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Male participants aged 50 years or older * Participants with physical activity or exercise program involvement * Participants with no history of serious medical conditions such as tumors, fractures, epilepsy, cardiac disease, or stroke within the past year. * Participants must be non-smokers and not receiving hormone or calcium supplement therapy

Exclusion criteria

* Participants unable to stand on the WBV platform * Participants with conditions contraindicating vibration therapy * Participants participating in other clinical trials

Design outcomes

Primary

MeasureTime frameDescription
Bone Density8 weeksChanges in BMD (measured by DXA scanner),
Grip Strength8 weekshand grip strength (measured by a hand-held dynamometer)
Vitamin D8 weeksVitamin D levels (measured by high-performance liquid chromatography).

Countries

Saudi Arabia

Contacts

Primary ContactFahad Alanazi, PhD
Fsalenezi@ju.edu.sa00966503409217

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026