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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05600543
Other study ID # 2022-A01060-43
Secondary ID ANSM
Status Recruiting
Phase N/A
First received
Last updated
Start date September 30, 2022
Est. completion date August 31, 2023

Study information

Verified date October 2022
Source Thuasne
Contact Paul CALMELS, MD PhD
Phone (0)477120383
Email paul.calmels@chu-st-etienne.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Low back pain (LBP) is a common condition worldwide as the lifetime prevalence is up to 80%. It is defined as pain in the lumbosacral region in which the etiological causes are most often mechanical, and it is therefore defined as "non-specific LBP". Lumbar belts are used in the treatment and secondary prevention of LBP. They are supposed to reduce the intensity of pain by improving the functional capacities of daily activities and thus preventing the risk of chronicity related to immobility (HAS). Despite some proof of their efficiency in the literature, it is still not clear how the pressure applied by the belt and the immobilization constraints on the trunk improve the patient mobility. Considering that LBP causes movement limitation, and that the lumbar belt contributes to initially decrease the pain intensity, as well as to improve the mobility and the functional capacities of the patient, we propose to evaluate the clinical and biomechanical effects of the lumbar belt during different trunk movements in subjects with and without LBP. This is a clinical investigation on a CE marked medical device, used in accordance with its intended purpose, in the context of a post-marketing clinical follow-up with additional non-invasive procedures (IC SCAC: case 4.1 of the medical device regulation 2017/745).This is a prospective, monocentric, comparative and open clinical investigation. The objective is to evaluate the clinical and functional effects related to spinal movements in 2 conditions, with and without the wearing of a lumbar belt. The study will be carried out with two groups of subjects: one group of subjects presenting an episode of LBP (NS>4) (subjects considered to have subacute or chronic nonspecific LBP according to the classification of LBP) and another group of control subjects with no spinal symptoms and no pain that could limit movement (healthy subjects). Each group will undergo 2 visits on 2 separate days with a 30-day delay for the LBP subjects and a 7-day delay for the healthy subjects - a first visit (V1) for inclusion, familiarization with a clinical and functional test, and an external measurement of spinal mobility during movements; - a second visit (V2) for a clinical and functional evaluation, external measurements of spinal mobility and biomechanical measurements.


Recruitment information / eligibility

Status Recruiting
Enrollment 32
Est. completion date August 31, 2023
Est. primary completion date August 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria for subjects Low Back Pain: - Male or female, - Aged between 18 and 70 years, - With a waist circumference between 75 cm and 110 cm, - With a 18.5 < BMI < 30 kg/m2, - Suffering from a current episode of non-specific low back pain (symptomatic subjects), - At least one average low back pain at rest or during exercise in the last 72 hours collected at inclusion (= 4/10 on an EN scale), - Followed by a primary care physician or specialist for this clinical condition, - Having received or scheduled to receive an EOS type radiological workup in less than 6 months - Affiliated or entitled to a social security system, - Having signed the written consent. Inclusion Criteria for healthy subjects: - Male or female, - Aged 18 to 70 years, - With a waist circumference between 75 cm and 110 cm, - With a 18.5 < BMI < 30 kg/m2, - Never having suffered from LBP or any other type of lumbar disorder, - Affiliated or entitled to a social security system, - Having signed the written consent. Exclusion Criteria: - Subjects suffering from LBP of inflammatory, tumoral or infectious cause. - Pregnant women. - Subjects with cognitive or mental disorders or confirmed depression; - Subjects who received an infiltration less than one month prior to the inclusion visit or planned during the study; - Subjects with a known allergy to any of the materials; - Subjects complaining of chronic, unstabilized or symptomatic cardiac or respiratory problems; - Subjects with current participation in an interventional investigational drug or device therapy study that impacts the endpoints. - Subjects under legal protection or unable to express their consent; - Subject presenting a lumbar radicular syndrome (hiatal hernia, spinal stenosis...).

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Lumbar belt
All subjects (LBP group and healthy group) wear the belt during the two visits to perform differents tests. The invistigator will ask the LBP patients to wear the lumbar belt between the two visits (for 4 weeks, for 4 to 8 hours per day)

Locations

Country Name City State
France CHU de St Etienne Saint-Étienne

Sponsors (1)

Lead Sponsor Collaborator
Thuasne

Country where clinical trial is conducted

France, 

References & Publications (13)

Christe G, Rochat V, Jolles BM, Favre J. Lumbar and thoracic kinematics during step-up: Comparison of three-dimensional angles between patients with chronic low back pain and asymptomatic individuals. J Orthop Res. 2020 Jun;38(6):1248-1256. doi: 10.1002/jor.24575. Epub 2020 Jan 7. — View Citation

Gombatto SP, Brock T, DeLork A, Jones G, Madden E, Rinere C. Lumbar spine kinematics during walking in people with and people without low back pain. Gait Posture. 2015 Oct;42(4):539-44. doi: 10.1016/j.gaitpost.2015.08.010. Epub 2015 Sep 3. — View Citation

Gombatto SP, D'Arpa N, Landerholm S, Mateo C, O'Connor R, Tokunaga J, Tuttle LJ. Differences in kinematics of the lumbar spine and lower extremities between people with and without low back pain during the down phase of a pick up task, an observational study. Musculoskelet Sci Pract. 2017 Apr;28:25-31. doi: 10.1016/j.msksp.2016.12.017. Epub 2017 Jan 5. — View Citation

Haj A, Weisman A, Masharawi Y. Lumbar axial rotation kinematics in men with non-specific chronic low back pain. Clin Biomech (Bristol, Avon). 2019 Jan;61:192-198. doi: 10.1016/j.clinbiomech.2018.12.022. Epub 2018 Dec 22. — View Citation

Hernandez A, Gross K, Gombatto S. Differences in lumbar spine and lower extremity kinematics during a step down functional task in people with and people without low back pain. Clin Biomech (Bristol, Avon). 2017 Aug;47:46-52. doi: 10.1016/j.clinbiomech.2017.05.012. Epub 2017 May 27. — View Citation

Marich AV, Hwang CT, Salsich GB, Lang CE, Van Dillen LR. Consistency of a lumbar movement pattern across functional activities in people with low back pain. Clin Biomech (Bristol, Avon). 2017 May;44:45-51. doi: 10.1016/j.clinbiomech.2017.03.004. Epub 2017 Mar 7. — View Citation

Marich AV, Hwang CT, Sorensen CJ, van Dillen LR. Examination of the Lumbar Movement Pattern during a Clinical Test and a Functional Activity Test in People with and without Low Back Pain. PM R. 2020 Feb;12(2):140-146. doi: 10.1002/pmrj.12197. Epub 2019 Sep 3. — View Citation

Masharawi Y, Haj A, Weisman A. Lumbar Axial Rotation Kinematics in an Upright Sitting and With Forward Bending Positions in Men With Nonspecific Chronic Low Back Pain. Spine (Phila Pa 1976). 2020 Mar 1;45(5):E244-E251. doi: 10.1097/BRS.0000000000003265. — View Citation

Mitchell K, Porter M, Anderson L, Phillips C, Arceo G, Montz B, Levy S, Gombatto SP. Differences in lumbar spine and lower extremity kinematics in people with and without low back pain during a step-up task: a cross-sectional study. BMC Musculoskelet Disord. 2017 Aug 25;18(1):369. doi: 10.1186/s12891-017-1721-z. — View Citation

Oshikawa T, Kaneoka K, Morimoto Y, Akuzawa H. Comparison of Lumbar Kinematics with a History of Low Back Pain During Baseball Hitting. Int J Sports Med. 2020 Feb;41(2):119-127. doi: 10.1055/a-1014-3041. Epub 2020 Jan 7. — View Citation

Shojaei I, Salt EG, Hooker Q, Van Dillen LR, Bazrgari B. Comparison of lumbo-pelvic kinematics during trunk forward bending and backward return between patients with acute low back pain and asymptomatic controls. Clin Biomech (Bristol, Avon). 2017 Jan;41:66-71. doi: 10.1016/j.clinbiomech.2016.12.005. Epub 2016 Dec 10. — View Citation

Vaisy M, Gizzi L, Petzke F, Consmuller T, Pfingsten M, Falla D. Measurement of Lumbar Spine Functional Movement in Low Back Pain. Clin J Pain. 2015 Oct;31(10):876-85. doi: 10.1097/AJP.0000000000000190. — View Citation

Van Hoof W, Volkaerts K, O'Sullivan K, Verschueren S, Dankaerts W. Comparing lower lumbar kinematics in cyclists with low back pain (flexion pattern) versus asymptomatic controls--field study using a wireless posture monitoring system. Man Ther. 2012 Aug;17(4):312-7. doi: 10.1016/j.math.2012.02.012. Epub 2012 Mar 20. — View Citation

* Note: There are 13 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary Spinal Mobility assessed by the fingertip to floor distance test (FTF) The effect of wearing a lumbar belt on spinal mobility during anterior flexion of the trunk (sagittal plane) in subjects with LBP using the fingertip to floor (FTF) distance test. Immediately with and without wearing the lumbar belt (Day 0)
Primary Spinal Mobility assessed by the fingertip to floor distance test (FTF) The effect of wearing a lumbar belt (for 4 weeks) on spinal mobility during anterior flexion of the trunk (sagittal plane) in subjects with LBP using the fingertip to floor (FTF) distance test. After 4 weeks with and without wearing the lumbar belt (Day 30)
Secondary Spinal Mobility assessed by the fingertip to floor distance test (FTF) Spinal mobility (using the FTF test in forward flexion, the FTF test in lateral flexion and the sternum to wall test in extension):
a.1) In subjects with LBP at Day 0 and Day 30
a.2) In healthy subjects (at Day 0)
a.3) Between healthy subjects and LBP subjects (at Day 0)
During the Day 0 (for both groups) and Day 30 (for LBP patients) with and without wearing the belt
Secondary Pain level assessed by Numerical Scale (NS) Pain in LBP subjects (Day 0 vs Day 30) using Numerical Scale (NS) from 0 to 10 (0: no pain and 10: worst pain) During the Day 0 and Day 30 immediately before and after wearing the belt, and after each movement with and without the belt (for LBP patients)
Secondary Functional capacities assessed by Oswestry Disability Index (ODI) Functional capacities of LBP subjects (Day 0 and Day 30) using Oswestry Disability Index (ODI) During the beginning of Day 0 and Day 30 (for LBP patients)
Secondary Kinematics of the spinal segments assessed by Inertial Measurement Units sensors Kinematics of the spinal segments using 3 IMUs (Inertial Measurement Units) sensors:
d.1) In LBP subjects (Day 0 vs Day 30) d.2) In healthy subjects (at Day 0) d.3) Between healthy subjects and LBP subjects (at Day 0)
During Day 0 (for both groups) and Day 30 (for LBP patients) with and without wearing the belt
Secondary Trunk posture measured by 8-camera image stereo correlation system Trunk posture using 8-camera image stereo-correlation system (Alternative to motion capture) e.1) In subjects with LBP (Day 30) e.2) In healthy subjects (at Day 7) e.3) Between healthy subjects and subjects with LBP (Day 7 vs Day 30) During Day 7 (for healthy subjects) and Day 30 (for LBP patients)
Secondary The pressure applied by the belt on the trunk assessed by piezo-resistive sensors The pressure applied by the belt on the trunk using piezo-resistive sensors f.1) In subjects with LBP (Day 30) f.2) In healthy subjects (at Day 7) f.3) Between healthy subjects and LBP subjects (Day 7 vs Day 30) During Day 7 (for healthy subjects) and Day 30 (for LBP patients)
Secondary Deformation of the lumbar belt assessed by 8-camera image stereo-correlation system To evaluate, during spinal movements, the deformation of the lumbar belt considered as a mechanism of action using 8-camera image stereo-correlation system:
g.1) In LBP subjects (Day 30) g.2) In healthy subjects (Day 7) g.3) Between healthy subjects and LBP subjects (Day 7 vs Day 30)
During Day 7 (for healthy subjects) and Day 30 (for LBP patients)
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