Cervical Stairstep and Effects on Range of Motion (ROM) (CSEROM)

August 22, 2008 updated by: Logan College of Chiropractic

The Effects of Cervical Stairstep on Cervical Range of Motion

Observe the effects of Cervical Stairstep on Cervical Spine Range of Motion

Study Overview

Status

Unknown

Intervention / Treatment

Detailed Description

The cervical spine can be affected in a number of ways due to its vulnerability to injury. These injuries can result from poor posture, sports or occupation and can lead to degenerative changes. Cervical range of motion (ROM) is also affected by these injuries. When active ROM is restricted, the injury is of muscular origin. Pain with passive ROM indicates ligamentous injury whereas restricted passive ROM indicates blockage within bone or soft tissue. The normal range of motion in the cervical spine is 80-90 degrees flexion, 70 degrees extension, 20-45 degrees lateral flexion and 90 degrees of rotation. A common mechanism of cervical spine injury is axial loading. Axial loading can create a buckling effect within the cervical spine and decrease its ability to move normally, creating a limited ROM.

Study Type

Interventional

Enrollment (Anticipated)

50

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Missouri
      • Chesterfield, Missouri, United States, 63017
        • Recruiting
        • Logan University, College of Chiropractic

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 48 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • students and faculty between ages 18 and 50

Exclusion Criteria:

  • current neck pain (as measured by the Neck Disability Index (NDI) and utilizing Jackson's and maximal foraminal compression tests to assess for radiating symptoms)
  • severe recent head trauma
  • acute exacerbations within the past 3 months
  • known cervical disc problems
  • surgical fusions within the cervical spine
  • highly acute symptoms
  • a positive valsalva test
  • seizure disorder
  • analgesics
  • muscle relaxants
  • medications with effects on the musculoskeletal system
  • chiropractic manipulation within 48 hours of the study
  • Other exclusions can be made based on investigator judgment

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental
Cervical low force mobilization procedure.
Cervical low force mobilization procedure.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Cervical Range of Motion
Time Frame: Pre and post treatment
Pre and post treatment

Secondary Outcome Measures

Outcome Measure
Time Frame
Neck Disability Index
Time Frame: pre and post treatment
pre and post treatment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2008

Primary Completion (Anticipated)

October 1, 2008

Study Completion (Anticipated)

October 1, 2008

Study Registration Dates

First Submitted

August 21, 2008

First Submitted That Met QC Criteria

August 22, 2008

First Posted (Estimate)

August 25, 2008

Study Record Updates

Last Update Posted (Estimate)

August 25, 2008

Last Update Submitted That Met QC Criteria

August 22, 2008

Last Verified

August 1, 2008

More Information

Terms related to this study

Other Study ID Numbers

  • SR0331080127

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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