We updated the design of this site on December 18, 2017. Learn more.
ClinicalTrials.gov
ClinicalTrials.gov Menu

Cervical Multifidus Muscle Function

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00733837
Recruitment Status : Completed
First Posted : August 13, 2008
Last Update Posted : December 18, 2008
Sponsor:
Information provided by:
Logan College of Chiropractic

Brief Summary:
The purpose of this study is to determine the relationship between cervical multifidi thickness, cervical spine proprioception and possible reflex activation of cervical multifidi through stimulation of joint mechanoreceptors. Cervical mechanoreceptors will be activated with an innocuous, nonspecific stimulation. Participants will have cervical spine proprioception assessed through joint position sense testing. The multifidus muscle thickness and activation state is to be assessed by sonography. These measures are done pre & post to the innocuous stimulation. There is no specific hypothesis.

Condition or disease Intervention/treatment Phase
Proprioception Muscle Activation Other: Nonspecific, Innocuous, Mechanoreceptor Stimulation Phase 1

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 30 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Study Start Date : July 2008
Primary Completion Date : October 2008
Study Completion Date : October 2008

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Balance Problems
U.S. FDA Resources

Arm Intervention/treatment
Experimental: A
This is a repeated measures study. All participants experience the same conditions.
Other: Nonspecific, Innocuous, Mechanoreceptor Stimulation
A custom device will be used to provide light manual cervical traction



Primary Outcome Measures :
  1. sonographic measurement of multifitus thickness [ Time Frame: pre - post ]

Secondary Outcome Measures :
  1. cervical spine repositioning error [ Time Frame: pre - post ]


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years to 30 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Logan student, staff, or faculty, ages 18 - 30 years

Exclusion Criteria:

  • Fractures
  • Tumors
  • Dislocations
  • Myopathies
  • Signs and/or symptoms of neuromotor disorders
  • Consumption of prescription drugs that affect the nervous system
  • Recent cervical spine injuries or surgeries
  • Pain
  • Manipulative therapy within the preceding 7 days
  • Neck pain

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00733837


Locations
United States, Missouri
Logan College
Chesterfield, Missouri, United States, 63017
Sponsors and Collaborators
Logan College of Chiropractic

Responsible Party: Kristan Giggey, DC, Logan University
ClinicalTrials.gov Identifier: NCT00733837     History of Changes
Other Study ID Numbers: RD0627080141
First Posted: August 13, 2008    Key Record Dates
Last Update Posted: December 18, 2008
Last Verified: December 2008