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Activity and Participation in Vestibular Disorders

Not Applicable
Recruiting
Conditions
Vestibular Disorder
Interventions
Other: Vestibular Rehabilitation
Registration Number
NCT06271694
Lead Sponsor
University of Pittsburgh
Brief Summary

This study will examine whether impairments and personal factors are associated with activity and participation in people with vestibulopathy. Data collection will occur prior to starting vestibular rehabilitation and after completing vestibular rehabilitation.

Detailed Description

Adults aged 18-years and older with symptomatic complaints of dizziness and/or imbalance and a medical diagnosis of unilateral vestibular hypofunction will be recruited at the time of their entry into vestibular rehabilitation. The investigators will analyze what factors (impairments and personal factors) are related to activity and participation in people with vestibular disorders and see if change in activity and participation is related to recovery from vestibulopathy.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
50
Inclusion Criteria
  • 18-years and older with symptomatic complaints of dizziness and/or imbalance and a medical diagnosis of unilateral vestibular hypofunction
Exclusion Criteria
    1. Cognition <18 on Montreal Cognitive Assessment (MoCA)
    1. Visual acuity worse than 20/40 with corrected lenses
    1. Loss of protective distal sensation (defined as the inability to feel a 4.31 size monofilament on the plantar surface of the foot)
    1. Inability to engage in community mobility

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Standard Vestibular RehabilitationVestibular RehabilitationAll participants will receive standard vestibular rehabilitation
Primary Outcome Measures
NameTimeMethod
Late-life Function and Disability Instrument8-weeks

Activity and Participation (raw 16-80; scale 0-100 min-max scores); higher is better

Dizziness Handicap Inventory8-weeks

Dizziness disability; 0-100 (min-max score); higher is greater disability.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

UPMC-Rehab Institute

🇺🇸

Pittsburgh, Pennsylvania, United States

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