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Proof of Concept Study Concerning Vestibular Stimulation Using a New Method of Dynamic Posturography.

Proof of Concept Study Concerning Vestibular Stimulation Using a New Method of Dynamic Posturography.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02851524
Acronym
POSTURODYN
Enrollment
30
Registered
2016-08-01
Start date
2016-06-23
Completion date
2017-04-21
Last updated
2026-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vestibular Stimulation

Brief summary

Falls in the elderly population are a major public health problem because of their frequency and their consequences, notably in terms of dependence their cost to society. In most cases, balance disorders related to an impaired vestibular system are blamed, even though there is no formal evidence that this is the case. Vestibular tests in routine otoneurological practice are based on the exploration of vestibulo-ocular or even vestibulo-cortical reflexes. They are not particularly suitable to screen for vestibular disorders in falls. A prototype rocking chair has been developed to test psycho-vestibular pathways, defined as the pathways via which vestibular afferents are transported to the subject's conscience. Thanks to this apparatus, a stimulus of body movement will be generated, but with limited tactile, visual and proprioceptive afferents, in such a way that the vestibular system alone is able to indicate to subjects their position in space. The subject will be required to detect oscillatory movement, and then to distinguish between a vestibular stimulus and a pulsed auditory stimulus. The study hypothesis is that the movement stimulation generated by our prototype will be sufficient to stimulate the vestibular system, which will manifest itself as a conscious sensation of movement and by a vestibulo-ocular reflex causing oculomotor manifestations.

Interventions

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Older than 18 years * National health insurance cover * Written consent * Subjects able to understand simple instructions and packaging information and to provide informed consent

Exclusion criteria

* Vertigo, consciousness disorders, nausea or pain before the tests * Bilateral deafness * History of neurological, rheumatic or orthopaedic disease likely by itself to trigger a fall * Psychiatric disorder likely to compromise participation. * Personal history of falls of undetermined cause. * Présence de saccades et/ou nystagmus en position statique * Femme enceinte

Design outcomes

Primary

MeasureTime frame
Cinematics of eye movements (amplitude and direction) evaluated by videonystagmography (VNG).At Day 0

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026