Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
30 participants
OBSERVATIONAL
2022-03-01
2022-08-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Non-Specific Low Back Pain patients
Participants must have pain located between the thoracolumbar hinge and the lower gluteal fold, with or without pain in either leg, present for more than 12 weeks, on a daily or almost daily basis (at least 4 days out of 7).
Quantified analysis of walking during a task of passage through a horizontal opening
Functional test that reproduce a task of daily living, similar to a doorway
Control group
Participant with no current or past chronic pain
Quantified analysis of walking during a task of passage through a horizontal opening
Functional test that reproduce a task of daily living, similar to a doorway
Interventions
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Quantified analysis of walking during a task of passage through a horizontal opening
Functional test that reproduce a task of daily living, similar to a doorway
Eligibility Criteria
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Inclusion Criteria
* This pain must have been present for more than 12 weeks, on a daily or almost daily basis (at least 4 days out of 7)
* Participants must not be on any treatment or have been on stable analgesic treatment for at least 2 weeks prior to inclusion
* Participants must speak, read and understand French
* Participants must be between 18 and 65 years of age
* Participants must be able to understand simple commands and experimental instructions
* Participants must have normal or corrected vision
* Participants must have given informed consent to participate in the study
* Participants must be enrolled in or receiving social security benefits
Exclusion Criteria
* Participants must not have cognitive or psychological impairments that are incompatible with compliance and/or understanding of the protocol (MMSE \> 28)
* Participants must not be unable to understand informed consent, or be under guardianship or conservatorship
* Subjects must not already be participating in another research protocol involving the human subject or in parallel
* Participants must not be persons deprived of liberty by judicial or administrative decision
* Participants must not be under psychiatric care
* The participants must not present neurological signs evoking a neurodegenerative disease responsible for walking disorders (parkinsonian syndrome, ...)
* The participants must not present warning signs (red flags) pointing to an underlying pathology requiring specific and/or urgent care such as
1. Ongoing litigation following a work-related accident
2. Pain related to a cancer diagnosis
3. Associated spinal cord symptoms (pyramidal signs, coordination disorders, motor or sensory deficits, sphincter disorders, etc.)
4. Pain following an infection (night sweats, fever, chills, intravenous drug abuse, immunodeficiency, recent surgery, urinary or skin infection, etc.)
5. Recent or pathological fractures (traffic accidents, history of osteoporosis, chronic use of corticosteroids, advanced age, unexplained weight loss, fatigue, history of cancer, etc. )
6. Vascular problems (cold feet, decreased peripheral arterial pulse, etc.)
18 Years
65 Years
ALL
Yes
Sponsors
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University of Rennes 2
OTHER
Responsible Party
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Agathe Bilhaut
PhD Student
Principal Investigators
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Olivier Roze, MD
Role: PRINCIPAL_INVESTIGATOR
clinique de la Sagesse
Locations
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University of Rennes 2
Rennes, , France
Countries
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References
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Bilhaut A, Menard M, Roze O, Cretual A, Olivier AH. Locomotion behavior of chronic Non-Specific Low Back Pain (cNSLBP) participants while walking through apertures. Gait Posture. 2023 Jul;104:140-146. doi: 10.1016/j.gaitpost.2023.06.015. Epub 2023 Jun 22.
Other Identifiers
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PERL
Identifier Type: -
Identifier Source: org_study_id
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