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Not yet recruiting NCT06644469

Whole Body Vibration in Middle Aged Men

No phase Interventional Bone Density Muscle Weakness

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Dynatronics VF5 Model vibration platform, Placebo Dynatronics VF5 Model vibration platform.
Who it may be relevant to
Registry conditions: Bone Density, Muscle Weakness. Basic parameters: from 50 years · Male.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Saudi Arabia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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

  • Device Dynatronics 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 suitab
  • Device Placebo Dynatronics VF5 Model vibration platform
    Placebo intensity with vertical vibration of 0.2 mm

Primary outcome measures

  • Bone Density [Time frame: 8 weeks]
  • Grip Strength [Time frame: 8 weeks]
  • Vitamin D [Time frame: 8 weeks]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Saudi Arabia · 1 center
  • prince Mutaib bin Abdulaziz hospital — Sakakah

Identifiers

NCT: NCT06644469 · JoufU

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗