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Longitudinal Recovery of Laboratory, Clinical, and Community-Based Measures of Head and Trunk Control in People With Acquired Vestibulopathy

Utah System of Higher Education (USHE) logo

Utah System of Higher Education (USHE)

Status

Terminated

Conditions

Vestibular Schwannoma
Vestibular Disorder

Treatments

Behavioral: Gaze and Postural Retraining Exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT04594057
IRB_00125069
NIFTI (Other Grant/Funding Number)

Details and patient eligibility

About

This study is designed to examine the true impact inner-ear dysfunction has on patient head movement kinematics, activity levels, and participation, and (2) to explore the efficacy of rehabilitation on laboratory, clinical, and community-based outcomes in people following surgical removal of a schwannoma from the inner-ear nerve.

Full description

In this project we will focus on characterizing deficits in community-based performance (i.e., head and trunk control during simulated community activities, short term community mobility, and patient reported participation) and relating these deficits to laboratory (i.e., video head impulse testing and corrective postural responses) and clinical (i.e., MiniBEST and dynamic visual acuity, and visual spatial cognition) measures of gaze and postural stability in individuals with varied forms of vestibulopathy (unilateral vestibular neuritis, bilateral vestibular loss, migraine related vestibulopathy, concussion, BPPV, Multiple Sclerosis). Additionally, we will examine the longitudinal change of laboratory, and community-based measures of gaze and postural in two cohorts of people with a specific form of unilateral vestibular loss (Vestibular Schwannoma resection); one group of these individuals will receive 6 weeks of vestibular rehabilitation during the acute onset of symptoms and the other one will begin intervention 6 weeks post onset. This portion of the proposed project will test my global hypothesis that changes in community-based performance of head and trunk control impair recovery following the onset of VH.

Aim 1: In individuals with vestibulopathy, characterize and compare laboratory and clinical measures of body structure, function, and performance to community-based, activity levels, performance, and patient reported participation. Hypothesis 1: The severity of laboratory and clinically measured gaze and postural stability function deficits will not strongly correlate with head and trunk control during community-based performance or patient reported participation. Hypothesis 2: The nature and severity of laboratory and clinically measured gaze and postural stability function deficits will differ between varied diagnostic groups.

Aim 2: In individuals with unilateral vestibular hypofunction following unilateral vestibular schwannoma resection, examine the longitudinal trajectories of laboratory and clinical measures of body structure, function and performance, and community-based performance, activity levels, and patient reported participation during periods of spontaneous and rehabilitation driven recovery. Hypothesis: Recovery of laboratory and clinical measures will follow different trajectories than measures of community-based performance and patient reported participation during both periods of spontaneous and rehabilitation driven recovery.

Enrollment

10 patients

Sex

All

Ages

18 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Reports of dizziness as indicated by Dizziness handicap inventory score >0
  • Undergoing a vestibular schwannoma resection surgery and/or vestibular hypofunction diagnosed using bedside examination
  • Able to perform community ambulation

Exclusion criteria

  • Presence of cardiovascular, orthopedic, or other neurologic diagnosis that limits ability to complete study testing, or causes other forms of dizziness.
  • Blindness
  • Peripheral neuropathy

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

10 participants in 2 patient groups

Early Start
Active Comparator group
Description:
Begin 6 weeks of gaze and postural stability training 10-14 days following surgery.
Treatment:
Behavioral: Gaze and Postural Retraining Exercise
Delayed Start
Experimental group
Description:
Begin 6 weeks of gaze and postural stability training 6 weeks following surgery.
Treatment:
Behavioral: Gaze and Postural Retraining Exercise

Trial contacts and locations

1

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Central trial contact

Lee Dibble, PhD; Brian Loyd, PhD

Data sourced from clinicaltrials.gov

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