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Activity and Participation in Vestibular Disorders

NCT ID: NCT06271694

Last Updated: 2025-12-18

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

RECRUITING

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-01-12

Study Completion Date

2026-03-31

Brief Summary

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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

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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.

Conditions

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Vestibular Disorder

Keywords

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Vestibular Rehabilitation Activity and Participation

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Standard Vestibular Rehabilitation

All participants will receive standard vestibular rehabilitation

Group Type OTHER

Vestibular Rehabilitation

Intervention Type OTHER

Standard vestibular rehabilitation

Interventions

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Vestibular Rehabilitation

Standard vestibular rehabilitation

Intervention Type OTHER

Eligibility Criteria

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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)
* 2\. Visual acuity worse than 20/40 with corrected lenses
* 3\. Loss of protective distal sensation (defined as the inability to feel a 4.31 size monofilament on the plantar surface of the foot)
* 4\. Inability to engage in community mobility
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute on Deafness and Other Communication Disorders (NIDCD)

NIH

Sponsor Role collaborator

University of Pittsburgh

OTHER

Sponsor Role lead

Responsible Party

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Brooke Klatt

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Brooke Klatt, PhD

Role: PRINCIPAL_INVESTIGATOR

Assistant Professor

Locations

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UPMC-Rehab Institute

Pittsburgh, Pennsylvania, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Chelsea Behling

Role: CONTACT

Phone: 412-624-8811

Email: [email protected]

Facility Contacts

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Chelsea Behling

Role: primary

Other Identifiers

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1K23DC020215-01

Identifier Type: NIH

Identifier Source: secondary_id

View Link

STUDY22020027

Identifier Type: -

Identifier Source: org_study_id