TerminatedNot Applicable

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

Stopped: Difficulty with enrollment secondary to COVID

United States10 participantsStarted 2019-12-10

Plain-language summary

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.

Who can participate

Age range18 Years – 85 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Change in Dizziness Handicap Inventory (DHI)

Timeframe: Change baseline to 6 weeks

Change in miniBEST test

Timeframe: Change from baseline to 6 weeks

Change in Community-simulated Ambulatory Task (CAT)

Timeframe: Change from Baseline to 6 weeks

Change in Passive Angular Vestibular Reflex Testing

Timeframe: Change from Baseline to 6 weeks

Trial details

NCT IDNCT04594057

SponsorUniversity of Utah

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-12-31

View on ClinicalTrials.gov More Vestibular Schwannoma trials