search
Back to results

The Effect of Plantar Vibration on the Progression of Peripheral Neuropathy

Primary Purpose

Peripheral Neuropathy

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
plantar vibration
Sponsored by
Binghamton University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Neuropathy focused on measuring peripheral neuropathy, diabetes, plantar vibration

Eligibility Criteria

30 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Clinical evidence of neuropathy
  • Normal to moderate evidence of neuropathy on nerve conduction studies

Exclusion Criteria:

  • Currently on medications with a known risk of neuropathy
  • Pregnant
  • Evidence of peripheral vascular disease

Sites / Locations

  • Neurology Associates

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

plantar vibration

Arm Description

Subject will use Juvent plantar vibration device daily in the home or office for six months.

Outcomes

Primary Outcome Measures

intraepidermal nerve fiber density in ankle and thigh

Secondary Outcome Measures

quality of life score
clinical assessment of peripheral neuropathy

Full Information

First Posted
January 13, 2009
Last Updated
January 13, 2009
Sponsor
Binghamton University
Collaborators
NY State Office of Science, Technology and Academic Research (NYSTAR)
search

1. Study Identification

Unique Protocol Identification Number
NCT00822198
Brief Title
The Effect of Plantar Vibration on the Progression of Peripheral Neuropathy
Official Title
The Effect of Plantar Vibration on the Progression of Peripheral Neuropathy
Study Type
Interventional

2. Study Status

Record Verification Date
January 2009
Overall Recruitment Status
Completed
Study Start Date
March 2006 (undefined)
Primary Completion Date
August 2007 (Actual)
Study Completion Date
August 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Binghamton University
Collaborators
NY State Office of Science, Technology and Academic Research (NYSTAR)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to assess the effect of vibration of the plantar surface of the foot on peripheral neuropathy.
Detailed Description
Background: Peripheral neuropathy has a prevalence approaching 10% in the general population. The pathophysiology of peripheral neuropathy is poorly understood or undetermined. While many causes of peripheral neuropathy are known, a significant number of cases are idiopathic. The most common cause of neuropathy relates to glucose intolerance or overt diabetes. Exogenous factors such as smoking constrict small cutaneous blood vessels, thereby inhibiting small nerve fiber nutrition. Symptoms of neuropathy include numbness, pain, difficulty with balance, lack of temperature perception, and weakness which can lead to significant disability. Classification of neuropathies can be made based on nerve fiber size: large fiber, small fiber and mixed large and small fiber types. Plantar vibration which affects large fibers has been demonstrated to enhance peripheral and systemic blood flow, peripheral lymphatic and venous drainage (Stewart, Karman, Montgomery, & McLeod, 2005). Since fluid retention in axons, nerve sheaths and surrounding connective tissues may contribute to neuropathy, it is hypothesized that plantar vibration may repair the small peripheral fibers, thereby improving the symptoms of neuropathy. Purposes: To assess the effect of plantar vibration on regeneration of small peripheral nerve fibers, peripheral neuropathy and quality of life in patients with diagnosed peripheral neuropathy. To assess the correlation of health history, demographic variables, diet, alcohol and smoking history with small fiber neuropathy analysis by skin biopsy and plantar vibration. Design: The study will employ a cross-over experimental design with subjects acting as their own controls. Independent variables are the plantar stimulation (intervention), and the characteristics of the subjects that include health history, demographic variables, self reported diet, alcohol, and smoking history, as well as urinary cotinine (a quantitative measure of smoking history). The dependent variables are the assay of intraepidermal nerve fibers in small-fiber neuropathy, clinical assessment of peripheral neuropathy, serum levels of Hgb A1C, and quality of life measurement.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Neuropathy
Keywords
peripheral neuropathy, diabetes, plantar vibration

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
plantar vibration
Arm Type
Experimental
Arm Description
Subject will use Juvent plantar vibration device daily in the home or office for six months.
Intervention Type
Device
Intervention Name(s)
plantar vibration
Intervention Description
Subjects in the experimental component of the trial will be provided with a Juvent 1000-CS device in their home or workplace. The device will be placed in a convenient location where the device does not represent a trip hazard, and yet is readily accessible for use. The subjects will be instructed to use the device whenever it is convenient to do so, either by standing on the device, or by sitting with their feet on the device. Downloads of usage data will be obtained intermittently. Period interviews with the subjects will be conducted to ensure that the device is operating and that no problems are encountered with device usage.
Primary Outcome Measure Information:
Title
intraepidermal nerve fiber density in ankle and thigh
Time Frame
0, 6 and 12 months
Secondary Outcome Measure Information:
Title
quality of life score
Time Frame
0, 6 and 12 months
Title
clinical assessment of peripheral neuropathy
Time Frame
0, 6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical evidence of neuropathy Normal to moderate evidence of neuropathy on nerve conduction studies Exclusion Criteria: Currently on medications with a known risk of neuropathy Pregnant Evidence of peripheral vascular disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leann M Lesperance, MD, PhD
Organizational Affiliation
Binghamton University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Neurology Associates
City
Corning
State/Province
New York
ZIP/Postal Code
14830
Country
United States

12. IPD Sharing Statement

Learn more about this trial

The Effect of Plantar Vibration on the Progression of Peripheral Neuropathy

We'll reach out to this number within 24 hrs