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

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00510757

Enrollment

200

Registered

2007-08-02

Start date

2007-06-30

Completion date

2010-06-30

Last updated

2008-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervicogenic Headache, Kyphotic and Reversed Cervical Curves, Neck Pain, Whiplash

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.

Interventions

None listed

Study design

Observational model

COHORT

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Yes

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

Countries

United States

Contacts

Primary ContactRodger E Tepe, PhD

rodger.tepe@logan.edu636-227-2100

Outcome results