Postural and Clinical Outcomes of SNAGs Treatment in Cervicogenic Dizziness Patients: a Randomised Controlled Trial
Cervicogenic Dizziness, Rehabilitation
About this trial
This is an interventional treatment trial for Cervicogenic Dizziness focused on measuring cervicogenic dizziness, sustained natural apophyseal glides, posturography testing, fast Fourier transform, cervical range of motion
Eligibility Criteria
Inclusion Criteria:
accepted criteria will be operationalized to achieve the clinical suspicion of cervicogenic dizziness as following:
- Exclusion of these differential diagnoses: a. Migrainous vertigo b. Vertigo of central origin c. Benign paroxysmal positional vertigo (BPPV) d. Meniere disease e. Vestibular neuritis f. Vertigo induced by drugs g. Psychogenic vertigo (anxiety and/or panic disorder and/or phobia) h. Orthostatic hypotension
- presence of a subjective feeling of dizziness associated with pain, movement, rigidity, or certain positions of the neck at least from 3 months;
- Cervical pain, trauma, and/or disease
- If from traumatic origin, there has to be a temporal proximity between the onset of dizziness and the neck injury.
Diagnosis is positive if criteria 1 to 3 are fulfilled. As for criterion 2, dizziness had to occur during the same period than neck pain occurred and dizziness had to be proportional to the severity of the neck pain that generally fluctuates in time.
Criterion 4 addresses cervicogenic dizziness occurring after a neck trauma
Exclusion Criteria:
- presence of trauma or recent surgery in the head, face, neck, or chest;
- an otorhinolaryngological diagnosis of central or peripheral vertigo
- receiving physiotherapy during the study period.
- History, physical examination and a thorough clinical otoneurological examination will be devised to exclude extracervical causes of dizziness.
- In order to exclude vestibular hypofunction, video Head Impulse Test - and the technique proposed in previous studies will be used to study the vestibulo-ocular reflex.
Sites / Locations
- UNITER ONLUS for balance and rehabilitation research
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
SNAGs treatment
Detuned Laser
cervicogenic patients will undergo SNAGs treatment. Based on personal history, the offending active cervical movement (i.e. the movement predominantly causing dizziness) will be identified and treatment direction will be determined. As suggested, the active movement to most likely cause dizziness is cervical extension, though also rotation or flexion will be shown to provoke it. With the participant in an upright sitting position, a skilled physiotherapist (blinded to the allocation) will apply a sustained passive accessory movement (glide) while the participant will be asked to move actively as allowed by his/her physiological range in the direction producing their symptoms. This procedure will be repeated six times.
cervicogenic patients will receive a sham treatment, carried out by the another skilled therapist (blinded to the allocation) and consisting in exposition to a detuned laser. A laser - deactivated by the manufacturer in order to produce no effective emission - will appear to operate normally, emitting a light signal and a beeping sound. Such procedure - which was shown to not activate somatosensory receptors and to have a very strong placebo effect - will be used for six applications, lasting 20 seconds, on various sites on the upper cervical spine, at a distance of 0.5-1cm from the skin.