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Clinical Trial Summary

To assess the impact of standardized written information on outcome in acute LBP.


Clinical Trial Description

A 3-month prospective, controlled study with a quasi-experimental design (i.e., a nonrandomized controlled sample with geographic stratification [30 areas]). Control and intervention areas ARE selected for their similarities in rural-to-urban distribution of the population and patients' access to GPs and to minimize risk of overlap between areas. ;


Study Design

N/A


Related Conditions & MeSH terms


NCT number NCT00343057
Study type Observational
Source Sanofi
Contact
Status Completed
Phase N/A
Start date September 2003
Completion date June 2004

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