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Unilateral Peripheral Vestibular Dysfunction: Reeducation and Spatial Orientation.

Unilateral Peripheral Vestibular Dysfunction: Reeducation and Spatial Orientation.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03171181
Enrollment
90
Registered
2017-05-31
Start date
2013-11-30
Completion date
2015-08-30
Last updated
2018-05-11

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

Conditions

Equilibrium; Disorder, Labyrinth, Inner Ear Disease, Spatial Navigation

Keywords

Spatial cognition, vestibular system, motor control

Brief summary

Motor control includes postural control and voluntary movement. For an optimal motor control it is necessary that brain integrates vestibular, visual and somatosensorial inputs properly, in a nonlinear way. Vestibular system, as an afferent organ, encodes head position in relation to gravity and changes in its linear and angular acceleration. As vestibular central system, it plays an essential role in motor control and in orientation and spatial memory as well. When a peripheral vestibular lesion occurs, elaboration, interpretation and processing of inputs are deficient and therefore motor control is altered to a greater or lesser degree. As process progress in time, there is a natural neuroplasticity that facilitates recovery or compensate vestibular function, although sometimes this process is incomplete and requires vestibular reeducation This study aims to assess changes in balance control, orientation and handicap perception in one case group with symptomatic unilateral peripheral vestibular dysfunction, before and after a rehabilitation programme (RV). To compare values obtained at the beginning and at the end of RV to those achieved by control group. Finally, this research aims to analyse evolution of spatial orientation quality in symptomatic and non symptomatic participants.

Detailed description

Intervention group: 30 people with a unilateral peripheral vestibular disorder (UPVD). Process lasting more than three months and symptomatic. Aged 18-66 years old. Control group: 30 participants without UPVD, healthy for the purpose of study. No intervention group: 30 people with a unilateral peripheral vestibular disorder without symptomatology. Both groups also aged 18-66. Balance quality was registered with static and dynamic posturography. For spatial orientation is was registered Visual vertical and visual orientation perception. Vestibular disability was also assessed. Variables were registered at the beginning and at the end of a vestibular reeducation in UPVD participants. Vestibular reeducation consisted of 10 sessions of vestibular rehabilitation using dynamic posturography and visual reeducation. Duration of each session: 40 minutes. Twice a week. The aim is to compare data before and after intervention with those obtained in compensated patients and control group.

Interventions

OTHERVestibular reeducation

Balance quality was registered with static and dynamic posturography. For spatial orientation is was registered Visual vertical and visual orientation perception. Vestibular disability was also assessed. Variables were registered at the beginning and at the end of a vestibular rehabilitation in UPVD participants. Vestibular rehabilitation consisted of 10 sessions of vestibular rehabilitation using dynamic posturography and visual reeducation. Duration of each session: 40 minutes. Twice a week.

Sponsors

Aragon Institute of Health Sciences
CollaboratorOTHER
Universidad de Zaragoza
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Longitudinal case-control study. Accidental sampling. Single - centre study (Hospital Universitario Miguel Servet, Zaragoza. Spain)

Eligibility

Sex/Gender
ALL
Age
18 Years to 66 Years
Healthy volunteers
Yes

Inclusion criteria

* People diagnosed of UPVD * Length of process superior to three months * Normal vision or corrected by lens or glasses.

Exclusion criteria

* Dizziness or balance alteration due to visual problem or lesion of CNS (central nervous system). * Balance disturbance due to a locomotor cause * Balance perturbation next to resolve. * Sharpening or acute phase os symptoms. * Difficulties with understanding commands.

Design outcomes

Primary

MeasureTime frameDescription
Changes in Visual vertical and visual orientation degrees at baseline and before treatment.Outcomes were measured in patients at baseline and 3 months. Control group and compensated group were registered at baseline.Visual vertical and visual orientation were measured with bucket test

Secondary

MeasureTime frameDescription
Balance quality.Outcomes were measured in patients at baseline and 3 months. Control group was registered at baseline.Balance quality was obtained from static and dynamic posturography

Other

MeasureTime frameDescription
Dizziness handicap inventory test.Outcomes were measured in patients at baseline and 3 months.Quality of life was registered with Dizziness handicap inventory test (DHI).

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026