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NCT00779610 Clinical Trial

The Effects of Passive and Active Vibration Therapy on Grip Strength and Myoelectric Activity

Strength Clinical Trial

Official title:
The Effects of Passive and Active Vibration Therapy on Grip Strength and Myoelectric Activity

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00779610
Other study ID # SR0810080147
Secondary ID
Status Recruiting
Phase Phase 1
First received October 23, 2008
Last updated October 23, 2008
Start date October 2008
Est. completion date November 2008

Study information
Verified date October 2008
Source Logan College of Chiropractic
Contact John Zhang, MD, PhD
Phone 636-230-1920
Email john.zhang@logan.edu
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This pilot study is designed to analyze the effects of Vibration Therapy (VT) on grip strength and level of forearm contraction by measuring hand grip dynamometry and surface Electromyography (sEMG) using the BioPac sEMG and digital dynamometry devices after the application of both passive and active Vibrational Therapy (VT) using the PowerPlate.

Recruitment information / eligibility
Status Recruiting
Enrollment 40
Est. completion date November 2008
Est. primary completion date November 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- participants will be Logan students, faculty and staff 18-65 yoa

- asymptomatic subject will be included in the study

- participants must complete a survey and consent form

- only participants that meet the criteria of the survey will be accepted in the study

Exclusion Criteria:

- participant with any recent or past disease/injuries/trauma/fracture (i.e., arthritis, carpal tunnel, etc.)

- who have had joint replacements

- who are currently engaging in physical rehabilitation

- who are pregnant will be excluded from the study

- history of cardiovascular disease

- history of cancer

- history of epilepsy

- history of diabetes mellitus, or past retinal surgeries

- participants cannot have Chiropractic manipulation or engage in weight lifting or other extreme exercise throughout the duration of the study

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Procedure:
• Vibration with flexion
Vibration with forearm flexion (active contraction)
• Vibration without flexion
Vibration without forearm flexion (passive)

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, 

Outcome
Type Measure Description Time frame Safety issue
Primary Surface EMG and Grip Strength Dynamometry Pre and Post treatment No
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