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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00733837
Other study ID # RD0627080141
Secondary ID
Status Completed
Phase Phase 1
First received August 11, 2008
Last updated December 17, 2008
Start date July 2008
Est. completion date October 2008

Study information

Verified date December 2008
Source Logan College of Chiropractic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the relationship between cervical multifidi thickness, cervical spine proprioception and possible reflex activation of cervical multifidi through stimulation of joint mechanoreceptors. Cervical mechanoreceptors will be activated with an innocuous, nonspecific stimulation. Participants will have cervical spine proprioception assessed through joint position sense testing. The multifidus muscle thickness and activation state is to be assessed by sonography. These measures are done pre & post to the innocuous stimulation. There is no specific hypothesis.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date October 2008
Est. primary completion date October 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- Logan student, staff, or faculty, ages 18 - 30 years

Exclusion Criteria:

- Fractures

- Tumors

- Dislocations

- Myopathies

- Signs and/or symptoms of neuromotor disorders

- Consumption of prescription drugs that affect the nervous system

- Recent cervical spine injuries or surgeries

- Pain

- Manipulative therapy within the preceding 7 days

- Neck pain

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Nonspecific, Innocuous, Mechanoreceptor Stimulation
A custom device will be used to provide light manual cervical traction

Locations

Country Name City State
United States Logan College Chesterfield Missouri

Sponsors (1)

Lead Sponsor Collaborator
Logan College of Chiropractic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary sonographic measurement of multifitus thickness pre - post No
Secondary cervical spine repositioning error pre - post No
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