Status:

UNKNOWN

Study to Demonstrate That Muscle Pattern Recognition (MPR) is an Effective Evaluation Tool for Musculoskeletal Neck or Back Pain

Lead Sponsor:

iTech Medical, Inc.

Conditions:

Neck Pain

Low Back Pain

Eligibility:

All Genders

18-62 years

Phase:

NA

Brief Summary

The investigators hypothesize that non able-bodied participants with reported acute, sub-acute, or chronic symptoms of neck or back pain of a musculoskeletal origin will have magnetic resonance imagin...

Detailed Description

Investigators aim to use data from both the able-bodied and non able-bodied samples to create a normative database for this technology. The primary objective of populating a normative database will be...

Eligibility Criteria

Inclusion

  • Individuals may participate in this study if they meet the following criteria:
  • 18-62 years of age; male or female.
  • 4 foot 10 inches to 6 foot 5 inches in height
  • No prior back or neck surgery, or structural deformity of the spine
  • No orthopedic injury/illness/surgery limiting range of motion of the shoulders
  • No ongoing treatments for back or neck pain/injury from a health professional in the last two years.
  • No prior loss of work time due to a neck or back injury/illness
  • Laboratory studies: complete blood count (CBC); sedimentation rate; creatinine phosphokinase (CPK); calcium; phosphorus; pregnancy test if female; and drug screen. Laboratory studies will be examined by a physician investigator to determine if the findings will exclude the participant from participating successfully in study activities. A positive pregnancy test or drug screen will automatically exclude the participant from the study.
  • Clinical examination of the neck and back by two physicians in agreement that the participant may participate in the study.
  • Absence of congenital or acquired neuromuscular disease or dysfunction

Exclusion

  • Individuals may not participate in this study if they meet the following criteria:
  • Claustrophobia or anxiety associated with being enclosed in narrow spaces
  • Muscle weakness or sensory feedback abnormalities that affect(s) gait
  • Pregnancy
  • Concurrent serious medical illness such as cancer; recent heart attack or stroke; heart rhythm disturbance requiring a pacemaker; diabetes that causes pain; numbness; or decreased circulation in the legs.
  • Alcohol or illicit drug abuse.
  • History of (or concurrent) psychiatric illness necessitating ongoing "talk" therapy and/or psychotropic medications
  • History of back or neck pain lasting more than 3 days or requiring time off of work AND healthcare provider treatments within the last 2 years
  • Involved in a lawsuit or receiving worker's compensation or disability payments
  • Individuals with pacemakers or pacemaker wires; aneurysm clips; or metallic foreign bodies or metal shavings in the body.

Key Trial Info

Start Date :

April 1 2005

Trial Type :

INTERVENTIONAL

End Date :

December 1 2006

Estimated Enrollment :

480 Patients enrolled

Trial Details

Trial ID

NCT00134225

Start Date

April 1 2005

End Date

December 1 2006

Last Update

October 26 2005

Active Locations (4)

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Page 1 of 1 (4 locations)

1

Department of Neurology - UC Irvine

Irvine, California, United States, 92697-4275

2

Midwest Consultants for Clinical Trials LLC

Portage, Michigan, United States, 49002

3

Advance Clinical Research

Salt Lake City, Utah, United States, 84102

4

Institute de Rescherche in Physiatrie du Quebec

Montreal, Quebec, Canada, H2K 1C1