Back Pain Clinical Trial
Official title:
Efficacy of Peak Scoliosis Brace in Pain Management For Adult Scoliosis Patients
Aim of the study is to evaluate a new brace that has become available, the Peak Scoliosis
Brace (Aspen Medical Products) designed to alleviate pain for adult patients with chronic
pain secondary to scoliosis.
20 adults with back pain secondary to Idiopathic Scoliosis will be recruited. The sample
size was calculated considering the data collected during the development of the brace in
the US. Patients will be evaluated at baseline immediately before starting with the brace
and after 4 weeks and 6 months. The brace must be worn for at least 2-4 hours per day.
At each evaluation they will be asked to fill the questionnaires, to be used as outcome
measure of the results.
Background: Some adult scoliosis patients suffer significant back pain and risk increased
curvature leading to postural collapse. The main approach for these patients according to
the current literature is the surgical one, however, surgery is not without complications,
is not appropriate for all patients and certain patients do not choose to undergo surgery.
Despite the fact that scoliosis has been estimated to affect up to 68% of the population
over 60, there is scant literature about conservative treatments for adult scoliosis; a case
report and a case series demonstrated the effectiveness of scoliosis specific exercise to
stop progression, while another study reported the effectiveness of a soft brace in reducing
pain at short time. Custom fabricated rigid torso braces, similar to those commonly used for
children are sometimes used in adult patients, however, the goal of these braces is to
correct and/or sustain the sagittal plane of patients, no data have been published on the
efficacy of these braces in relief of pain, and such braces are typically not well tolerated
by adults. Recently a new brace has become available, the Peak Scoliosis Brace (Aspen
Medical Products) designed to alleviate pain for adult patients with chronic pain secondary
to scoliosis.
Aim: to test the efficacy of the Peak Scoliosis Brace in reducing pain in adult scoliosis
patients.
Study design: prospective cohort study. Population: 20 adults with back pain secondary to
Idiopathic Scoliosis. The sample size was calculated considering the data collected during
the development of the brace in the US, and the first 2 patients fitted in Italy. Setting
alpha at 0.05 and the power at 0.8, with a mean expected improvement of 2 point in the pain
NRS, 16 patients would be necessary.
Considering the possibility of 25% drop out the investigators decided to recruit 20
subjects.
Statistical analysis: If data will be normally distributed, the investigators will use a
paired t-test. Otherwise, non-parametric statistical tests will be applied.
Protocol: patients will be evaluated at baseline immediately before starting with the brace
and after 4 weeks and 6 months. The brace must be worn for at least 2-4 hours per day. At
each evaluation they will be asked to fill the NRS, Rolland Morris Questionnaire and COMI.
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