- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00741000
Cervical Stairstep and Effects on Range of Motion (ROM) (CSEROM)
August 22, 2008 updated by: Logan College of Chiropractic
The Effects of Cervical Stairstep on Cervical Range of Motion
Observe the effects of Cervical Stairstep on Cervical Spine Range of Motion
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
The cervical spine can be affected in a number of ways due to its vulnerability to injury.
These injuries can result from poor posture, sports or occupation and can lead to degenerative changes.
Cervical range of motion (ROM) is also affected by these injuries.
When active ROM is restricted, the injury is of muscular origin.
Pain with passive ROM indicates ligamentous injury whereas restricted passive ROM indicates blockage within bone or soft tissue.
The normal range of motion in the cervical spine is 80-90 degrees flexion, 70 degrees extension, 20-45 degrees lateral flexion and 90 degrees of rotation.
A common mechanism of cervical spine injury is axial loading.
Axial loading can create a buckling effect within the cervical spine and decrease its ability to move normally, creating a limited ROM.
Study Type
Interventional
Enrollment (Anticipated)
50
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 Contact
- Name: Mary Unger-Boyd, DC
- Phone Number: 1780 636-230-2100
- Email: mary.unger-boyd@logan.edu
Study Locations
-
-
Missouri
-
Chesterfield, Missouri, United States, 63017
- Recruiting
- Logan University, College of Chiropractic
-
-
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
16 years to 48 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- students and faculty between ages 18 and 50
Exclusion Criteria:
- current neck pain (as measured by the Neck Disability Index (NDI) and utilizing Jackson's and maximal foraminal compression tests to assess for radiating symptoms)
- severe recent head trauma
- acute exacerbations within the past 3 months
- known cervical disc problems
- surgical fusions within the cervical spine
- highly acute symptoms
- a positive valsalva test
- seizure disorder
- analgesics
- muscle relaxants
- medications with effects on the musculoskeletal system
- chiropractic manipulation within 48 hours of the study
- Other exclusions can be made based on investigator judgment
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: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Experimental
Cervical low force mobilization procedure.
|
Cervical low force mobilization procedure.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Cervical Range of Motion
Time Frame: Pre and post treatment
|
Pre and post treatment
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Neck Disability Index
Time Frame: pre and post treatment
|
pre and post treatment
|
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 (Anticipated)
October 1, 2008
Study Completion (Anticipated)
October 1, 2008
Study Registration Dates
First Submitted
August 21, 2008
First Submitted That Met QC Criteria
August 22, 2008
First Posted (Estimate)
August 25, 2008
Study Record Updates
Last Update Posted (Estimate)
August 25, 2008
Last Update Submitted That Met QC Criteria
August 22, 2008
Last Verified
August 1, 2008
More Information
Terms related to this study
Other Study ID Numbers
- SR0331080127
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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