Multi Cervical Unit Measures of Cervical Isometric Strength and Range of Motion: A Pilot Study

The recruitment status of this study is unknown because the information has not been verified recently.
Verified October 2008 by Logan College of Chiropractic.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Logan College of Chiropractic
ClinicalTrials.gov Identifier:
NCT00510757
First received: July 31, 2007
Last updated: October 16, 2008
Last verified: October 2008
  Purpose

This study is designed to collect normative data on cervical isometric strength and range of motion to supplement an existing normative data base.


Condition
Cervicogenic Headache
Neck Pain
Whiplash
Kyphotic and Reversed Cervical Curves

Study Type: Observational
Study Design: Observational Model: Cohort

Resource links provided by NLM:


Further study details as provided by Logan College of Chiropractic:

Estimated Enrollment: 200
Study Start Date: June 2007
Estimated Study Completion Date: June 2010
Estimated Primary Completion Date: June 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts
Males
Females

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Consenting males and females between the ages of 18 and 65.

Criteria

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00510757

Contacts
Contact: Rodger E Tepe, PhD 636-227-2100 ext 1925 rodger.tepe@logan.edu

Locations
United States, Missouri
Logan University, College of Chiropractic Recruiting
Chesterfield, Missouri, United States, 63017
Contact: Tepe         
Sponsors and Collaborators
Logan College of Chiropractic
Investigators
Principal Investigator: Rodger E Tepe, PhD Logan College
  More Information

No publications provided

Responsible Party: Rodger Tepe, PhD, Logan College of Chiropractic
ClinicalTrials.gov Identifier: NCT00510757     History of Changes
Other Study ID Numbers: RD0426070090
Study First Received: July 31, 2007
Last Updated: October 16, 2008
Health Authority: United States: Institutional Review Board

Additional relevant MeSH terms:
Post-Traumatic Headache
Brain Diseases
Central Nervous System Diseases
Headache Disorders
Headache Disorders, Secondary
Nervous System Diseases

ClinicalTrials.gov processed this record on October 20, 2014