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

Unknown statusNot applicableNCT00134225
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

Brief summary (from the registry)

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 imaging (MRI), X-ray and blood parameters that do not demonstrate a statistical difference between "normal" (able-bodied) volunteers. Muscle pattern recognition (MPR) testing will show statistically different results between these groups. This statistically significant finding in MPR results will enhance a clinician's determination of clinical normality or abnormality. If this hypothesis is demonstrated, the MPR modality will be the first quantitative tool developed for assisting in the diagnosis of the presence or absence of a musculoskeletal dysfunction in a patient population. The availability of such an evaluation tool to a healthcare provider for patients with soft tissue, non-surgical neck or back complaints will substantially improve the accuracy of diagnosis and case management decisions.

Study details

Official title
Multi-Center, Multi-National Study to Demonstrate That Muscle Pattern Recognition is a Reliable and Valid Evaluation Tool for Patients Who Present With Acute, Sub-Acute, or Chronic Symptoms of Neck or Back Pain of a Musculoskeletal Origin
Interventions
  • Device: Muscle Pattern Recognition (MPR)
Sponsor
iTech Medical, Inc.
Start date
2005-04
Sex
All
Age range
from 18 Years to 62 Years
Healthy volunteers
true
Results posted
No results posted in this snapshot
Countries
Canada, United States
Total sites listed
4

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 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 Criteria: 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.

Canadian sites (1)

FacilityCityProvince
Institute de Rescherche in Physiatrie du QuebecMontrealQuebec

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT00134225