Multi Cervical Unit Measures of Cervical Isometric Strength and Range of Motion: A Pilot Study
1 other identifier
observational
200
1 country
1
Brief Summary
This study is designed to collect normative data on cervical isometric strength and range of motion to supplement an existing normative data base.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2007
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2007
CompletedFirst Submitted
Initial submission to the registry
July 31, 2007
CompletedFirst Posted
Study publicly available on registry
August 2, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2010
CompletedOctober 17, 2008
October 1, 2008
3 years
July 31, 2007
October 16, 2008
Conditions
Study Arms (2)
Males
Females
Eligibility Criteria
Consenting males and females between the ages of 18 and 65.
You may qualify if:
- Logan students, faculty and staff
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Logan University, College of Chiropractic
Chesterfield, Missouri, 63017, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Rodger E Tepe, PhD
Logan College
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
July 31, 2007
First Posted
August 2, 2007
Study Start
June 1, 2007
Primary Completion
June 1, 2010
Study Completion
June 1, 2010
Last Updated
October 17, 2008
Record last verified: 2008-10