Multi Cervical Unit Measures of Cervical Isometric Strength and Range of Motion: A Pilot Study
NCT ID: NCT00510757
Last Updated: 2008-10-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
200 participants
OBSERVATIONAL
2007-06-30
2010-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
Study Groups
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Males
No interventions assigned to this group
Females
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* 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
18 Years
65 Years
ALL
Yes
Sponsors
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Logan College of Chiropractic
OTHER
Responsible Party
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Logan College of Chiropractic
Principal Investigators
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Rodger E Tepe, PhD
Role: PRINCIPAL_INVESTIGATOR
Logan College
Locations
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Logan University, College of Chiropractic
Chesterfield, Missouri, United States
Countries
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Central Contacts
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Facility Contacts
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Tepe
Role: primary
Other Identifiers
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RD0426070090
Identifier Type: -
Identifier Source: org_study_id