Low Back Pain Clinical Trial
Official title:
Immediate and Short-term Effects of Mulligan "Sustained Natural Apophyseal Glides" for a Subgroup of Low Back Pain Patients: A Randomized Placebo Controlled Trial
Objectives:
Determine the efficacy of the SNAG technique (Mulligan) applied to a subgroup of people with
non-specific low back pain (LBP) on two new kinematic-algorythms, on pain, functional
disability and kinesiophobia.
Design:
A randomized double blinded placebo controlled trial with double arms in accordance with the
CONSORT statement.
Subjects:
Patients with non-specific low back pain will be recruting from Saint-Luc hospital, only a
subgroup of them will be included according to specific inclusion criteria tailored for
indication of application of SNAG's therapy (Mulligan technique applied on the lumbar
spine).
Method:
Subjects will be randomized in 2 groups; real-SNAG and sham-SNAG groups. All patients will
be treated during a single session, and real/sham SNAG will be applied from a sitting
position with the belt, and in a flexion direction. Two kinematic-algorythms (ROM and Speed)
from a validated kinematic spine model will be used and recorded with an opto-electronic
device (BTS-Elite). Pain at rest and during flexion, as well as functional disability and
kinesiophobia will be recorded by self-reported measures. These outcomes will be blindly
evaluated before and after treatment to compare both groups with " Two-Way-ANOVA " statistic
with for factors; time and groups.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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