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Completed

NCT Number: NCT01258543

Osteopathic Evaluation on Patients With Non-specific Back Pain: An Inter-examiner Reliability Study

The purpose of this study is to determine whether two osteopathic evaluators with less than 5 years experience will be able to determine the same location and nature of the primary lesion(s) or restriction(s)in patients with chronic non-specific back pain using a global osteopathic evaluation approach.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Concordia Physio Sport

Brossard, Quebec, J4Z 1A7, Canada

About this study

Back pain is one of the leading causes of consultation for rehabilitation. Establishing a diagnosis in the initial patient assessment is essential to choosing a specific treatment plan for that patient, regardless of the type of therapy the patient chooses to pursue. Evidence based medicine is the current gold standard for most manual-therapy professions, and there has been a great deal of research performed in an attempt to give credibility to the one tool that all manual therapy professions share in common: palpation. Few studies have been able to demonstrate an acceptable rate of inter-examiner reliability for palpation. This study will combine a global testing regime, consensus training for evaluators, and access to history of injury with symptomatic subjects to verify the inter-examiner reliability of an osteopathic evaluation on patients with chronic, non-specific low back pain.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men and women ages 18-60
  • Must have a history of non-specific back pain (not due to any known pathology eg. disc herniation or disc degenerative disease) that is currently not irritated and has not been, in the past 8 weeks
  • Must be available for 3 consecutive hour

Exclusion criteria

  • Patients with a known cause for their back pain
  • Patients who have had a flare up of symptoms within the last 8 weeks
  • Patients who are currently undergoing any rehabilitation or who have received manual treatment in the last 8 weeks.
  • Patients who are taking daily medications for pain
  • Pregnant women
  • Major medical conditions: fractures, degenerative arthritis, inflammatory disorders, ankylosing spondylitis, multiple sclerosis, cancer, paralysis stroke or recent concussion history
  • Any other conditions that would prevent the participant from completing the evaluation

Treatment and study plan

General Osteopathic Evaluation

Other

2 general osteopathic evaluations of approximately 1 hour in duration done consecutively on the same day with a 15 minute break between evaluations

Primary outcomes

  1. Inter-examiner reliability

    Time frame: Day 1

    Inter-examiner reliability between two evaluators for nature and location of primary restriction(s), lesion(s) found during a global osteopathic evaluation

Sponsors and collaborators

Lead sponsor

Kirnan, Jaime

Indiv

Registry information

Official study title

Osteopathic Evaluation on Patients With Non-specific Back Pain: An Observational Inter-examiner Reliability Study

Important dates

Study start
2010
Primary completion
2011
Study completion
2011
First posted
Dec 13, 2010
Registry last updated
Jun 13, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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