Lower Back Pain Clinical Trial
Official title:
Traditional Rehabilitation Versus Rehabilitation With the Imoove® Device for Spinal Musculoskeletal Disorders: a Randomised Controlled Trial
The main objective of this study is to evaluate in patients with chronic low back pain (lasting for more than 3 months and not postoperative) the effect of an instrumental rehabilitation using the I-Moove ® device compared to a conventional physiotherapy rehabilitation for ambulatory postural stability (mean and standard deviation of excursions from the center of gravity) without visual control, 6 weeks after the start of the rehabilitation protocol. We focus on the relative variation between the values obtained on day 0 versus 6 weeks, via measures performed on a force platform. The results will be stratified into 3 age groups (18-39 years, 40-60 years and over 60 years).
The secondary objectives of this study are to evaluate and compare the two physical therapy
techniques at 6 weeks and 6 months after the start of the rehabilitation protocol in terms
of:
A - improving postural stability and visual control on an unstable surface (with and without
visual control)
B - improving levels of abdominal strength (Ito test) and erector spinae (Sørensen test)
C - the impact of back pain on daily life using questionnaires (Dallas, Québec, FABQ and
Tampa questionnaires/scores)
D - Improvement of pain (Visual Analog Scale),
;
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