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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00316251
Other study ID # SR0403060006
Secondary ID
Status Completed
Phase N/A
First received April 18, 2006
Last updated November 20, 2006
Start date April 2006
Est. completion date September 2006

Study information

Verified date April 2006
Source Logan College of Chiropractic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the effects of Power Plate vibration therapy on balance as measured by the NeuroCom Balance Master.


Description:

Acute and chronic equilibrium disorders result in over five million patient visits per year in the United States with unknown additional individuals not seeking care. Symptoms of dizziness, vertigo, and lack of balance are among the most common symptoms reported to physicians. Equilibrium disorders not exclusively due to visual or vestibular conditions are typically due to problems in proprioception. Proprioception is the specialized sensory modality that informs the body as to movement, position, and spatial orientation through mechanisms that track sensations accompanying joint movement and position. Mechanoreceptors in joints, along with vestibular, visual, muscle spindle, Golgi tendon organ, ligament and tendon sensory receptors, comprise the propriosensory system, which conveys information to the motor system to maintain equilibrium on a reflexive, automatic basis. Alterations in somatosensory input from mechanoreceptors have been identified as causing aberrant muscle firing patterns.

The NeuroCom Balance Master is an FDA approved device designed to both measure and treat balance problems and evaluate the neuromuscular control by quantifying the ability to maintain dynamic postural stability. The NeuroCom Unit is a microprocessor controlled balance unit that provides quantitative data regarding the patient’s ability to control the platform. This unit is widely used throughout the country in both university and clinical settings to help patients restore their balance.


Recruitment information / eligibility

Status Completed
Enrollment 2
Est. completion date September 2006
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Logan student, staff, or faculty with no history of ankle injury

- Ages 18 – 60 years old

- Logan student, staff, or faculty with no history of ankle surgery

- No visual or vestibular condition that would affect balance

Exclusion Criteria:

- Systemic illnesses that have an adverse effect on balance

- Local infection, injury, or other malignancy affecting the lower extremity

- Any unstable joints of the lower extremity

- Any spinal manipulation within 48 hours

- Prescription or herbal muscle stimulants, relaxants, etc. that could affect balance

- Pregnancy

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Vibration Plate Therapy


Locations

Country Name City State
United States Logan College of Chiropractic Chesterfield Missouri

Sponsors (1)

Lead Sponsor Collaborator
Logan College of Chiropractic

Country where clinical trial is conducted

United States, 

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