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NCT00706043 Clinical Trial

French Validation Orebro Musculoskeletal Pain Screening Questionnaire (OMPSQ) Questionnaire

Chronic Low Back Pain Clinical Trial

Official title:
Validation of a French Translation of the Orebro Musculoskeletal Pain Screening Questionnaire (OMPSQ): A Prospective One-year Follow-up Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00706043
Other study ID # BA001
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2008
Est. completion date December 2012

Study information
Verified date March 2019
Source Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Low back pain is a very common disease. Among the persons suffering of acute low back pain, about 10% are at risk of developping chronic pain. A screening questionnaire assessing this risk has been developed and validated in Swedish and English (Orebro Musculoskeletal Pain Screening Questionnaire, Linton, 2003). The aim of our study is to validate a french translation of this questionnaire. Patients suffering from acute low back pain will be asked to fill in several questionnaires at day 0, and 6 and 12 month later.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date December 2012
Est. primary completion date December 2010
Accepts healthy volunteers No
Gender All
Age group 20 Years to 55 Years
Eligibility Inclusion Criteria:

- all consecutive patients presenting at the clinical care setting with acute low back pain

- pain lasting for less than three months

- cumulated sick leave less thant six months

Exclusion Criteria:

- unability to sufficiently read and understand French

- presence of red flags as according to the New Zealand Acute Low Back Pain Guide

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Outcome
Type Measure Description Time frame Safety issue
Primary Pain 6 and 12 month
Secondary Professional status 6 and 12 months
Secondary functional status 6 and 12 months
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