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Clinical Trials/ACTRN12623000444684
ACTRN12623000444684
Recruiting
N/A

The effect of noisy galvanic vestibular stimulation on postural control in people with bilateral vestibulopathy

Auckland University of Technology0 sites31 target enrollmentMay 1, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Bilateral vestibulopathy
Sponsor
Auckland University of Technology
Enrollment
31
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 1, 2023
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • a.Probable diagnosis of Bilateral vestibulopathy (BVP) (determined by a neurologist, ENT consultant, GP, audiologist or specialist vestibular clinic).
  • b.Self\-reported unsteadiness when walking
  • plus either
  • oscillopsia during walking or quick head/body movements or
  • worsening of balance in darkness or on uneven ground.
  • c.No symptoms when sitting or lying under static conditions (self\-reported)
  • d.Aged between 18 and 80 years
  • After consent participants will undertake a vestibular assessment to ensure they meet the clinical criteria for BVP of
  • Bilaterally reduced vestibular function indicated by either
  • a.Horizontal angular VOR gain (\<0\.8\) measured by video Head Impulse Testing or

Exclusion Criteria

  • Participants will be excluded from the study if they have:
  • a. They have any evidence of CNS involvement including hereditary ataxias or brain stem/ cerebellar abnormalities, or any central eye movement abnormalities or previously diagnosed neurological condition. (Participants will be screened by staff at the clinics they are recruited via).
  • b.Unable to stand independently for 5 minutes or ambulate for 10m without aid
  • c.Individuals who are medically required to restrict their head movement
  • d.Metal implants in the head or neck such as cochlea implants, clips, coilings, shunts or endoprosthesis
  • e.Pacemaker or implanted defibrillator
  • f.Previous open skull surgery or trepanation
  • g.Broken skin in the region of electrode placement

Outcomes

Primary Outcomes

Not specified

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