NCT01186718

Brief Summary

The purpose of this project is to quantify 3-dimensional (3-D) cervical motion pattern changes that result from osteopathic manipulation treatment (OMT) in an experimental subject group diagnosed with somatic dysfunction. The kinematic data will include the entire 3-D motion trajectories of the head, resulting in range of motion (ROM) and angular data for the primary and secondary motions.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Sep 2009

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2009

Completed
12 months until next milestone

First Submitted

Initial submission to the registry

August 20, 2010

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 23, 2010

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2011

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2011

Completed
Last Updated

November 29, 2011

Status Verified

November 1, 2011

Enrollment Period

1.9 years

First QC Date

August 20, 2010

Last Update Submit

November 28, 2011

Conditions

Human Cervical Motions

Keywords

Cervical, motions, kinematics

Outcome Measures

Primary Outcomes (1)

  • 3-D kinematic measurements of cervical motion

    9/2009 to 8/2011

Study Arms (2)

Control Group

Control group = functional symmetric cervical motion.

Experimental subject group

Experimental subject group = asymmetric cervical motion

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Two study groups: Control = subjects with symmetric cervical motion; Experimental = subjects with asymmetric cervical motion.

You may qualify if:

  • Cervical motion symmetry and asymmetry

You may not qualify if:

  • Under 18 years of age

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Michigan State University

East Lansing, Michigan, 48824, United States

Location

Related Publications (1)

  • Vorro J, Bush TR, Rutledge B, Li M. Kinematic measures during a clinical diagnostic technique for human neck disorder: inter- and intraexaminer comparisons. Biomed Res Int. 2013;2013:950719. doi: 10.1155/2013/950719. Epub 2013 Feb 16.

    PMID: 23509819DERIVED

Study Officials

  • Joseph Vorro, Phd

    Michigan State University Dept. Family Medicine

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor and PI

Study Record Dates

First Submitted

August 20, 2010

First Posted

August 23, 2010

Study Start

September 1, 2009

Primary Completion

August 1, 2011

Study Completion

August 1, 2011

Last Updated

November 29, 2011

Record last verified: 2011-11

Locations

US(1)