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Completed

NCT Number: NCT00396994

"VIBES"--Low Magnitude Mechanical Stimulation to Improve Bone Mineral Density

The purpose of this study is to determine if daily low magnitude, high frequency whole body vibration can improve bone density in seniors.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hebrew SeniorLife, Institute for Aging Research

Boston, Massachusetts, 02131, United States

About this study

The treatment options for osteoporosis, a major health complication in the aged population, are limited to pharmacologic interventions, the majority of which are antiresorptive. Preliminary data demonstrate that high frequency, low magnitude mechanical stimulation (LMMS) can preserve bone mineral density (BMD) by preventing bone resorption due to disuse and aging, and can stimulate new bone formation.

To confirm and extend these observations, this study is a three-year, double-blind, randomized, placebo-controlled clinical trial of LMMS in 200 elderly women and men (60 years of age and older). A clinical center located in Boston, MA has recruited participants from multiple independent living facilities in close geographic proximity. Participants meeting the inclusion/exclusion criteria have been randomized to either brief daily exposure to LMMS on a vibrating platform or a placebo platform over a three year period. All participants receive 1000 mg of elemental calcium and 800 IU of vitamin D per day.

This study will provide new and important information about the role of low magnitude high frequency mechanical stimulation on the skeleton.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men and women 60 years and over of all ethnic groups
  • Weight less than 250 pounds
  • Absence of terminal cancer or other illness necessitating hospice level services
  • Capable of following the protocol and of understanding and providing informed consent
  • Scoring less than 12 on the Short Blessed Test

Exclusion criteria

  • Immobilization of the axial or lower appendicular skeleton within the last year
  • Nonambulatory (ambulation with an assistive device will be permitted)
  • Malignancy other than cured thyroid cancer or skin cancer
  • Hip replacement or internal fixation, total knee replacement, or lower limb fracture within the past year, or bilateral hip replacement
  • Medications: glucocorticoids, suppressive doses of thyroid hormone as determined by screening TSH, anticonvulsant drugs (phenytoin, phenobarbital, carbamazepine), estrogen/testosterone replacement, selective estrogen receptor modulators (SERMs), PTH, or bisphosphonates more than 1 month in past year, calcitonin therapy within the preceding month, fluoride therapy at any time
  • Paget's disease of bone, rheumatoid arthritis or other connective tissue disorders requiring systemic treatment with disease modifying drugs, or a history of Cushing's syndrome
  • Fragility fracture within the past five years unless pharmacologic therapy not to be prescribed

Treatment and study plan

Low magnitude mechanical stimulation

Device

10 minutes per day of low magnitude mechanical stimulation using a vibrating platform set at 0.3 g and 30 Hz

Sham low magnitude mechanical stimulation

Device

10 minutes per day of low magnitude mechanical stimulation using a sham vibrating platform

Primary outcomes

  1. Changes in volumetric trabecular BMD of the spine and hip by quantitative computed tomography (CT scan)

    Time frame: 2 - 3 years

Secondary outcomes

  1. Changes in biochemical markers of bone formation (Procollagen type 1 N-terminal peptide and Bone Specific Alkaline Phosphatase) and resorption (C-terminal Telopeptide of type I collagen)

    Time frame: 2 - 3 years

  2. Changes in postural stability

    Time frame: 2 - 3 years

    Postural stability measured as quiet stance with eyes open for 4 minutes on a Kistler force platform

  3. Changes in isometric leg extension strength

    Time frame: 2 - 3 years

    Isometric knee extension strength of the right leg measured with a handheld dynamometer

  4. Change in hip muscle area and density

    Time frame: 2 - 3 years

    Muscle area and density surrounding the hips measured by quantitative computed tomography

Sponsors and collaborators

Lead sponsor

Hebrew SeniorLife

Other

Collaborators

  • National Institute on Aging (NIA)

Registry information

Official study title

Low Magnitude Mechanical Stimulation (LMMS) to Improve Bone Mineral Density (BMD)

Important dates

Study start
2007
Primary completion
2012
Study completion
2012
First posted
Nov 8, 2006
Registry last updated
Mar 20, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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