Concurrent Vestibular Activation and Postural Training Using Virtual Reality

NCT ID: NCT05942781

Last Updated: 2025-06-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-04-15

Study Completion Date

2025-09-01

Brief Summary

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Postural instability is a common symptom of vestibular dysfunction that impacts a person's day-to-day activities. Vestibular rehabilitation is effective in decreasing dizziness, visual symptoms and improving postural control through several mechanisms including sensory reweighting. As part of the sensory reweighting mechanisms, vestibular activation training with headshake activities influence vestibular reflexes. However, combining challenging vestibular and postural tasks to facilitate more effective rehabilitation outcomes is under-utilized. The novel concurrent headshake and weight shift training (Concurrent HS-WST) is purported to train the vestibular system to directly impact the postural control system simultaneously and engage sensory reweighting to improve balance. Healthy older adults will perform the training by donning a virtual reality headset and standing on the floor or foam pad with an overhead harness on and a spotter present to prevent any falls. The investigators propose that this training strategy would show improved outcomes over traditional training methods by improving vestibular-ocular reflex (VOR) gains, eye movement variability, sensory reweighting and promoting postural balance. The findings of this study may guide clinicians to develop rehabilitation methods for vestibular postural control in neurological populations with vestibular and/or sensorimotor control impairment.

Detailed Description

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Conditions

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Vestibular Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Vestibular activation training

A cross-over design will be used with group one receiving the training intervention for 7 days, a 6-day washout period, and a 7-day no-training period. Group two will follow the reverse sequence.

Group Type EXPERIMENTAL

Vestibular training using VR followed by Control

Intervention Type DEVICE

A cross-over design will be used with group one receiving the training intervention for 7 days, a 6-day washout period, and a 7-day no-training period.

Control followed by Vestibular training using VR

Intervention Type DEVICE

Group two will follow the reverse sequence.

No training

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Vestibular training using VR followed by Control

A cross-over design will be used with group one receiving the training intervention for 7 days, a 6-day washout period, and a 7-day no-training period.

Intervention Type DEVICE

Control followed by Vestibular training using VR

Group two will follow the reverse sequence.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Able to stand independently (without an assistive device)

* This study requires participants to perform postural assessments including reactive balance following mechanical perturbations.
* Participants will also perform headshake activities and weight shift training in standing for 20 mins will mini breaks.
* Participants must be between the ages of 55-80.

Exclusion Criteria

* Participants with evidence of:

* Concussion, vestibular, balance or oculomotor issues for the prior 6 months.
* Neuropathic conditions, particularly affecting the lower extremities. Participants with this issue will have sensory impairments which can affect their sensory assessment.
* Current musculoskeletal deficits including significant postural abnormalities (signs of spinal, pelvic and leg length discrepancies).
* Pain or limitations in neck range of motion.
* Recent (within 6 months) orthopedic surgery that impacts postural training.
* Visual Impairment ○ Participants must be able to see and follow targets in the virtual reality environment. Therefore, subjects must have 20/50 (corrected) vision. Subjects who are blind cannot participate.
Minimum Eligible Age

55 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Clarkson University

OTHER

Sponsor Role lead

Responsible Party

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Kwadwo Appiah-Kubi

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Clarkson Hall

Potsdam, New York, United States

Site Status

Countries

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United States

Other Identifiers

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23-30

Identifier Type: -

Identifier Source: org_study_id

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