Neck Pain Clinical Trial
This study is designed to collect normative data on cervical isometric strength and range of motion to supplement an existing normative data base.
Status | Recruiting |
Enrollment | 200 |
Est. completion date | June 2010 |
Est. primary completion date | June 2010 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Logan students, faculty and staff Exclusion Criteria: - recent surgery,or unstable or fused joints of the cervical spine - using medications, prescription or herbal muscle stimulants, relaxants, etc - previous cervical spine injury, surgery or condition that would affect your range of motion in the cervical spine - currently have any local infection, injury or other malignancy affecting the cervical spine - congenital conditions affecting the cervical spine, i.e. block vertebrae - systemic illness with an adverse effect on the cervical spine - a history of dizziness, light headedness or passing out, or any seizure disorder - had a neck, shoulder or back injury - ever been in an automobile accident - exercise regularly - pregnant - spinal manipulation mobilization or other therapy in the last 48 hours |
Observational Model: Cohort
Country | Name | City | State |
---|---|---|---|
United States | Logan University, College of Chiropractic | Chesterfield | Missouri |
Lead Sponsor | Collaborator |
---|---|
Logan College of Chiropractic |
United States,
Status | Clinical Trial | Phase | |
---|---|---|---|
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