Low Back Pain
Conditions
Keywords
rehabilitation, active range of motion, kinesiophobia, physiotherapy
Brief summary
The main objective of this study is to assess efficacy of a spine rehabilitation program, using spine flexion and extension full active range of motion, on physical disability of patients with chronic low back pain.
Detailed description
Secondary objectives The other objectives of this study are to assess the impact of spine rehabiliation program using spine flexion and extension full active range of motion on : * pain intensity ; * kinesiophobia * active range of motion of lumbar flexion and lumbar extension Conduct of research After receiving the written consent of the study, participants will benefit from 5 sessions of spine flexion and extension full active range of motion exercises. The following tests and questionnaires will be performed before (baseline) and after (posttreatment) the 5 sessions : * Visual Analogue Pain Scale, * Fear Avoidance Beliefs Questionnaire (FABQ), * Double-inclinometer to measure active range of motion of lumbar flexion and lumbar extension.
Interventions
PROCEDURESpine flexion/extension active range of motion exercises
Five full active range of motion rehabilitation sessions will be scheduled. Four or the five following full active range of motion exercises will be performed during one rehabilitation session : spine flexion and extension (quadrupedic position), lumbar flexion and extension (sitting position), posterior and anterior pelvic tilt (sitting and standing position), lumbar flexion and extension (standing position) and Jefferson Curl exercise. All five rehabilitation sessions must be performed within 60 days
Sponsors
Groupe Hospitalier de la Region de Mulhouse et Sud Alsace
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Medical prescription for chronic low back pain rehabilitation * Evolution of low back pain for at least 3 months * No treatment or rehabilitation for low back pain performed within 12 months before enrollment * Written informed consent given
Exclusion criteria
* Spinal fracture or previous spinal surgery * Cognitive impairments that prevent from understanding the rehabilitation exercises * Patient with insufficient understanding or expression in French * Non-mechanical pain : gradually worsening pain, present at rest and especially at night * Neurological symptom : deficit in the control of bladder and anal sphincters, motor weakness of lower limbs, Cauda equina syndrome * Pubis paresthesia (or perineum) * Severe trauma (such as fall from height, traffic accident) * Unexplained weight loss * History of cancer * Drug use or long-term use of corticosteroid * Spinal deformity * Altered general condition * Patient with signs of neurological impairment : positive Lasegue test (Straight Leg Raise Test) or positive Slump test, or DN4 questionnaire greater than or equal to 4 * Patient suffering from a central or peripheral neurological pathology * Patient taking a level II (weak opiates) or III (morphine and related substances) analgesic treatment * Patient under guardianship, curatorship or legal protection
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Roland-Morris disability questionnaire | Posttreatment (2 months) | The Roland-Morris questionnaire is a 24-item self report questionnaire assessing physical disability, ranging from 0 (no disability) to 24 (severe disability). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pain intensity | Posttreatment (2 months) | Pain intensity will be measured with a Visual Analog Pain Scale, from 0 (no pain) to 10 (pain of maximum intensity) |
| Fear Avoidance Beliefs Questionnaire (FABQ) | Posttreatment (2 months) | The FABQ is a patient reported questionnaire which specifically focuses on how patient's fear-avoidance beliefs about physical activity may affect and contribute to his/her low back pain and resulting disability. |
| Active range of motion of lumbar flexion and lumbar extension | Posttreatment (2 months) | Active range of motion of lumbar flexion and lumbar extension will be measured with two inclinometers. |
Countries
France
Outcome results
None listed