Skip to main content
Clinical Trials/NCT04347148
NCT04347148
Completed
Not Applicable

Postural and Clinical Outcomes of SNAGs Treatment in Cervicogenic Dizziness Patients: a Randomised Controlled Trial

Uniter Onlus1 site in 1 country80 target enrollmentMarch 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cervicogenic Dizziness
Sponsor
Uniter Onlus
Enrollment
80
Locations
1
Primary Endpoint
Cervical Spine Movements
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Previous works demonstrated the relationship between postural disturbances and reduction in cervical range of motion (CROM) in patients suffering from cervicogenic dizziness (CGD). Since sustained natural apophyseal glides (SNAGs) have been proposed as an effective treatment, the aim of the present study was to evaluate how clinical measures could be affected in patients with cervicogenic dizziness undergoing SNAGs.

Registry
clinicaltrials.gov
Start Date
March 1, 2018
End Date
March 2, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Uniter Onlus
Responsible Party
Principal Investigator
Principal Investigator

Alessandro Micarelli

Scientific Director

Uniter Onlus

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.

Outcomes

Primary Outcomes

Cervical Spine Movements

Time Frame: one month

A cervical range of motion (CROM) goniometer, which has been shown to be a reliable tool with good validity, will be used to measure (in degrees) cervical spine movements. Active flexion, extension, left and right rotation, and left and right lateral flexion will be measured three times and then averaged. Low levels of outcomes indicate worse performances. No specific reference ranges are given in literature.

Balance Test

Time Frame: one month

Study of the surface of the ellipse of confidence (calculated in mm) by means of static posturography platform will be used to assess the sway of the posture. Low levels of outcomes indicate better performances. No specific reference ranges are given in literature.

Secondary Outcomes

  • Disability of the Neck(one month)
  • Pain of the Neck(one month)
  • Self-report dizziness(one month)
  • Anxiety and Depression(one month)
  • Fear of Movement(one month)

Study Sites (1)

Loading locations...

Similar Trials