Low back pain is a major public health problem. It is the leading cause of disability in the world. The factors that lead to chronicity of low back pain are multi-factorial and are essentially represented by psychosocial factors (catastrophism, kinesiophobia, algophobia job dissatisfaction, emotional problems such as depression, anxiety, stress, injustice, etc.). Pain is a multimodal experience that involves different brain structures that are activated by the pain signal and involve the autonomic nervous system (ANS). The vagus nerve is the main actor of one of the two branches of the ANS, the parasympathetic system, which acts as a "slow-down". The vagus nerve participates in the inter-neuronal transmission of key neurotransmitters for mood, alertness, attention and motivation. Vagal stimulation has been used for many years as an analgesic device in chronic pain (vascular pain (facial vascular pain, fibromyalgia, visceral pain, gastrointestinal and pelvic pain...) To date, no study has been conducted on the value of vagal stimulation in chronic low back pain.
Low back pain is a major public health problem. It is the leading cause of disability in the world. The factors that lead to chronicity of low back pain are multifactorial, which explains the modest effectiveness of both drug treatments and multidisciplinary programs (analgesic drug interventions, non-pharmacological interventions with rehabilitation, physical exercise, psychotherapy, spinal ergonomics, meditation, yoga, etc.) in the treatment of low back pain. psychotherapy, spinal ergonomics, meditation, yoga...) in chronic forms. These factors of chronicization are essentially represented by psychosocial factors (catastrophism, kinesiophobia, algophobia, job dissatisfaction, emotional problems such as depression, anxiety stress, injustice...) In the chronic low back pain population, pain is a multimodal experience that involves different brain structures (insula, anterior cingulate cortex, amygdala and prefrontal cortex). These structures are activated by the pain signal and involve the autonomic nervous system (ANS). The vagus nerve is the main actor of one of the two branches of the ANS, the parasympathetic system, which acts as a "slow-down". The vagus nerve is involved in the inter-neuronal transmission of key neurotransmitters for mood, alertness, attention and motivation (serotonin, dopamine, oxytocin and noradrenaline). It is one of the longest nerves in the human body, originating from the base of the brain (nucleus tractus solitarius) and innervating most of the organs (heart, lung, stomach, liver, spleen, kidneys, gallbladder, pancreas, intestines). It allows the integration of information from the periphery (pain, stress, emotions), slows down the heart rate after a stress, reduces the caliber of the bronchial tubes to help breathing, reduces the inflammatory response, participates in digestion and in the communication with the digestive microbiota. Indeed, there seems to be an alteration of the vagal function in chronic pain patients patients: the vagus nerve is involved in the modulation of pain at different levels (medullary, cerebral) (medullary, cerebral) but also on the different components of pain (sensory, affective emotional, behavioral). The benefit of the stimulation of the vagus would be mediated by a modulation of afferent information (stress, pain, emotion) associated with a benefit of "relaxation" conveyed by the efferent fibers (cardiac, pulmonary effect...). This stimulation of the vagus nerve is done through an atrial electrode that stimulates the atrial branch of the vagus nerve. To date, no study has been conducted on the value of vagal stimulation in chronic low back pain. Because of the multifactorial mechanisms involved in this pathology, this type of therapy appears to be a useful complement to the management of our patients. This pilot study will allow us to evaluate the feasibility of a larger study with a placebo arm. The evaluation of tolerance and adherence to this therapy will be taken into account.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Use of the auricular electrode throughout the duration of the study (30minutes/day) combined with assessment of pain, tolerance, vagal tone.
CHU Montpellier
Montpellier, France, France
CHU Nîmes - Le Grau du Roi
Nîmes, France
change from baseline pain at 1 month
evaluated by a Visual Analog Scale (VAS, 0 the worst result and 100 the best result)
Time frame: between baseline and 1 month
change from baseline functional disability at 1 month
evaluated by Oswestry score The questionnaire consists of 10 questions, concerning: pain, self-care, load carrying, walking, sitting, standing, sleep, sexual life, social life, travel. Score between 0 and 20%: minimal disability Score between 21 and 40%: moderate disability Score between 41 and 60% : severe disability Score between 61 and 80% : major disability Score between 81 and 100% : bedridden patient
Time frame: between baseline and 1 month
change from baseline functional disability at 3 month
evaluated by Oswestry score The questionnaire consists of 10 questions, concerning: pain, self-care, load carrying, walking, sitting, standing, sleep, sexual life, social life, travel. Score between 0 and 20%: minimal disability Score between 21 and 40%: moderate disability Score between 41 and 60% : severe disability Score between 61 and 80% : major disability Score between 81 and 100% : bedridden patient
Time frame: between baseline and 3 month
change from baseline quality of life at 1 month
evaluated by EQ-5D-5L score (0 to 20, 0 the better, and 20 the worst ; 0 to 100 for the L part, 0 the worst and 100 the better)
Time frame: between baseline and 1 month
change from baseline quality of life at 3 month
evaluated by EQ-5D-5L score (0 to 20, 0 the better, and 20 the worst ; 0 to 100 for the L part, 0 the worst and 100 the better)
Time frame: between baseline and 3 month
change from baseline anxiety and depression at 1 month
evaluated by HAD (Hospital Anxiety and Depression scale) score
Time frame: between baseline and 1 month
change from baseline anxiety and depression at 3 month
evaluated by HAD (Hospital Anxiety and Depression scale) score
Time frame: between baseline and 3 month
change from baseline catastrophism at 1 month
evaluated by PCS (Pain Catastrophizing Scale) score
Time frame: between baseline and 1 month
change from baseline catastrophism at 3 month
evaluated by PCS (Pain Catastrophizing Scale) score
Time frame: between baseline and 3 month
evolution of use of painkillers at 1 month
Time frame: between baseline and 1 month
evolution of use of painkillers at 3 month
Time frame: between baseline and 3 month
evaluation of device adherence at 1 month
number of stimulations performed
Time frame: between baseline and 1 month
evaluation of device adherence at 3 month
number of stimulations performed
Time frame: between baseline and 3 month
evaluation of device tolerance at 1 month
number of adverse events
Time frame: between baseline and 1 month
evaluation of device tolerance at 3 month
number of adverse events
Time frame: between baseline and 3 month
evaluation of device satisfaction at 1 month
Lickert scale from 1 to 5.
Time frame: between baseline and 1 month
evaluation of device satisfaction at 3 month
Lickert scale from 1 to 5.
Time frame: between baseline and 3 month
change from baseline vagal tone at 1 month
evaluated by Heart Rate variability
Time frame: between baseline and 1 month
change from baseline vagal tone at 3 month
evaluated by Heart Rate variability
Time frame: between baseline and 3 month
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