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Biomechanical Gait Analysis in Low Back Pain

Biomechanical Analysis of Gait in Individuals With Low Back Pain

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07417345
Acronym
LBP
Enrollment
74
Registered
2026-02-18
Start date
2025-10-01
Completion date
2026-03-26
Last updated
2026-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain

Keywords

Gait, Chronic pain, Low Back Pain, Kinematics

Brief summary

The goal of this observational case-control study is to learn whether low back pain is associated with changes in gait and related clinical characteristics in adults over 18 years old. The main questions it aims to answer are: * Are gait biomechanics different in people with low back pain compared with people without low back pain? * Are pain intensity, psychosocial risk, and physical activity levels different between both groups? Participants will complete questionnaires about low back pain, physical activity, and health status, and will perform a walking test in a motion analysis laboratory where gait parameters are recorded.

Detailed description

This study is an observational case-control investigation designed to explore the relationship between low back pain and gait biomechanics in adults. Low back pain is a common health problem that may affect movement patterns, physical function, and daily activities. Understanding how gait is modified in people with low back pain may help to improve assessment and rehabilitation strategies. Participants will be divided into two groups: adults with low back pain and adults without low back pain. Sociodemographic and clinical characteristics will be collected to describe the sample and to allow comparisons between groups. The study will focus on the analysis of spatiotemporal, kinematic, and dynamic gait parameters obtained in a motion analysis laboratory. Gait assessment will be performed using a three-dimensional motion capture system. In addition to gait analysis, participants will provide information about their health status, pain characteristics, physical activity, and psychosocial factors through self-report questionnaires. These variables will be used to describe the clinical profile of the participants and to examine potential associations with gait outcomes. Comparisons between the low back pain group and the control group will be conducted to identify differences in gait biomechanics and clinical characteristics.

Interventions

None listed

Sponsors

Arrate Pinto Carral
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adults aged 18 years or older. * Ability to read and understand Spanish. * For the low back pain group: current low back pain or low back pain within the last month lasting at least 24 hours. * For the control group: absence of current low back pain and no episode of low back pain during the previous month. * Willingness to participate and provision of written informed consent.

Exclusion criteria

* Presence of leg pain or radicular symptoms (sciatica). * Pregnancy or childbirth within the last 12 months. * Previous lumbar spine surgery. * History of cancer, spinal tumor, or spinal infection. * Vertebral compression fracture. * Central nervous system disease. * Cauda equina syndrome. * Abdominal aortic aneurysm. * Any surgery or traumatic injury of the lower limbs within the last 5 years. * Any medical condition that could affect gait performance.

Design outcomes

Primary

MeasureTime frameDescription
Gait speedAt baseline assessmentMean walking speed during gait measured in meters per second (m/s) using 3D motion analysis.
Step and stride lengthBaselineStep length and stride length measured in meters (m) during gait analysis
CadenceBaselineNumber of steps per minute during walking recorded with motion capture system (steps/min)
Temporal gait parametersBaselineStance time and gait cycle time measured in seconds during gait
Pelvis kinematicsBaselinePelvic angles during gait in sagittal, frontal, and transverse planes, reported as maximum angle, minimum angle, and range of motion (ROM calculated as max-min). Measured in degrees.
Hip kinematicsBaselineHip joint angles during gait in sagittal, frontal, and transverse planes, reported as maximum angle, minimum angle, and range of motion (ROM = max-min). Measured in degrees.
Knee kinematicsBaselineKnee joint angles during gait in sagittal, frontal, and transverse planes, reported as maximum angle, minimum angle, and range of motion (ROM = max-min). Measured in degrees.
Ankle kinematicsBaselineAnkle joint angles during gait in sagittal, frontal, and transverse planes, reported as maximum angle, minimum angle, and range of motion (ROM = max-min). Measured in degrees.

Secondary

MeasureTime frameDescription
Pain intensity - Numeric Pain Rating Scale (NPRS)BaselinePain intensity measured with the Numeric Pain Rating Scale (NPRS) ranging from 0 to 10, where 0 = no pain and 10 = worst imaginable pain. Higher scores indicate worse pain intensity.
Psychosocial risk - STarT Back Screening Tool (SBST)BaselinePsychosocial risk assessed with the STarT Back Screening Tool (SBST). The total score ranges from 0 to 9 and participants are classified using the standard algorithm: Low risk: total score 0-3; Medium risk: total score ≥4, with psychosocial subscale \<4; High risk: psychosocial subscale score ≥4. Higher categories indicate worse prognosis and greater risk of persistent disability.
Physical activity level - International Physical Activity Questionnaire (IPAQ-SF)BaselinePhysical activity assessed with the International Physical Activity Questionnaire - Short Form (IPAQ-SF). Participants are classified into three categories according to standard scoring criteria: Low physical activity: not meeting criteria for moderate or high levels, Moderate physical activity: at least 600 MET-minutes/week through moderate activity or walking; High physical activity: at least 1500 MET-minutes/week of vigorous activity on ≥3 days, or ≥3000 MET-minutes/week of any combination of activities. Higher categories indicate greater levels of physical activity.
Hip flexor (iliopsoas) shortening - Modified Thomas TestBaselineIliopsoas muscle shortening assessed using the Modified Thomas Test. The result is classified as positive when the thigh remains elevated above the table, and negative when the thigh rests on the table surface. Positive result indicates presence of iliopsoas shortening.
Rectus femoris shortening - Modified Thomas TestBaselineRectus femoris muscle shortening assessed using the Modified Thomas Test. The result is classified as positive when knee flexion is less than 80°, and negative when knee flexion is 80° or greater. Positive result indicates presence of rectus femoris shortening.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 16, 2026