Assessment of the Evolution of Lumbar Spine Movement Fluidity Using Xsens Inertial Sensors in Subjects With Chronic Low Back Pain Before and After Rehabilitation (Xmouv)

University Hospital Center (CHU)

Status: Not yet enrolling

Conditions: Low Back Pain

Treatments: Device: X-sens sensor

Study type: Interventional

Funder types: Other

Identifiers

NCT07327554

RECHMPL25_0310

2025-A02160-49 (Other Identifier)

Details and patient eligibility

About

Low back pain, defined as pain located between the thoracolumbar junction and the lower gluteal fold, becomes chronic in 8% of patients. As the leading cause of disability worldwide, it has major individual and medico-economic consequences.

Three-dimensional biomechanical analysis allows exploration of movement alterations related to low back pain. Although several parameters have already been studied (maximum joint range of motion (ROM), lumbopelvic rhythm, movement variability, gait), no consistent kinematic profile has emerged. Movement fluidity, assessed by the presence of jerks (brief movement disturbances), remains under-described despite its relevance in evaluating movement quality.

Invistigators hypothesize that lumbar spine movement fluidity during flexion improves after a rehabilitation program and correlates with clinical response.

This project stands out by exploring a rarely studied parameter (movement fluidity) and integrating it as a potential indicator for rehabilitation monitoring.

Enrollment: 25 estimated patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age between 18 and 65 years inclusive
• BMI between 18-30 kg/m²
• Chronic low back pain lasting more than three months
• Rehabilitation care in the Physical Medicine and Rehabilitation Department of Montpellier University Hospital

Exclusion criteria

• Sciatica episode within the last three months
• Traumatic, tumoral, or infectious cause of low back pain
• History of spinal, pelvic, or hip fracture
• Inflammatory rheumatism
• Lumbar arthrodesis
• Severe scoliosis
• Subject with a legal protection measure (guardianship, curatorship)
• Subject under legal protection
• Subject not affiliated to a social security system or not benefiting from such a system
• Absence of informed written consent
• Pregnant or breastfeeding women

Trial design

Primary purpose: Supportive Care

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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25 participants in 1 patient group

Compare Movement Fluidity Before and After Rehabilitation

Experimental group

Description:

Evolution of Movement Fluidity Before and After Rehabilitation in patients with chronic low back pain

Treatment:

Device: X-sens sensor