- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00733837
Cervical Multifidus Muscle Function
December 17, 2008 updated by: Logan College of Chiropractic
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
30
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Missouri
-
Chesterfield, Missouri, United States, 63017
- Logan College
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 30 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: A
This is a repeated measures study.
All participants experience the same conditions.
|
A custom device will be used to provide light manual cervical traction
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
sonographic measurement of multifitus thickness
Time Frame: pre - post
|
pre - post
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
cervical spine repositioning error
Time Frame: pre - post
|
pre - post
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2008
Primary Completion (Actual)
October 1, 2008
Study Completion (Actual)
October 1, 2008
Study Registration Dates
First Submitted
August 11, 2008
First Submitted That Met QC Criteria
August 12, 2008
First Posted (Estimate)
August 13, 2008
Study Record Updates
Last Update Posted (Estimate)
December 18, 2008
Last Update Submitted That Met QC Criteria
December 17, 2008
Last Verified
December 1, 2008
More Information
Terms related to this study
Other Study ID Numbers
- RD0627080141
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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