Prognostic Factors of Disabling Low Back Pain in Patients With Chronic Low Back Pain
NCT ID: NCT02226692
Last Updated: 2015-05-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
53 participants
OBSERVATIONAL
2011-10-31
2014-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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nonspecific chronic low back pain
Physical examination and follow-up assessment by questionnaires at 2, 4, 6, and 12 months
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* nonspecific low back pain : pain located between the twelfth rib and the inferior gluteal fold for which no specific source of pain could be identified
* chronic low back pain : pain present for 12 weeks or more, and included both constant and recurrent patterns of pain
* able to read and understand French
Exclusion Criteria
* Current use of medication known to impair physical effort and pain perception
* Lumbar scoliosis of more than 20°
* Collagenosis, severe osteoporosis
* Neuromuscular disease
* Malignant tumor
* Non-controlled hypertension
* Infection
* Radiculopathy
* Progressive neurologic defect
* Myelopathy
* Lumbar disc hernia
* Pregnancy
* Active lower body injury and/or severe and disabling pain limiting the capacity to undergo the evaluation.
18 Years
60 Years
ALL
No
Sponsors
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Fonds de la Recherche en Santé du Québec
OTHER_GOV
Institut de Recherche Robert-Sauvé en Santé et en Sécurité du Travail
OTHER
Université du Québec à Trois-Rivières
OTHER
Responsible Party
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Martin Descarreaux
Dr Martin Descarreaux DC, PhD
Principal Investigators
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Martin Descarreaux, PhD
Role: PRINCIPAL_INVESTIGATOR
Université du Québec à Trois-Rivières
Locations
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Université du Québec à Trois-Rivières
Trois-Rivières, Quebec, Canada
Countries
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References
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Page I, Abboud J, O Shaughnessy J, Laurencelle L, Descarreaux M. Chronic low back pain clinical outcomes present higher associations with the STarT Back Screening Tool than with physiologic measures: a 12-month cohort study. BMC Musculoskelet Disord. 2015 Aug 19;16:201. doi: 10.1186/s12891-015-0669-0.
Other Identifiers
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UQTR-2011-PFAC
Identifier Type: -
Identifier Source: org_study_id
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