Actively Recruiting

Phase Not Applicable
Age: 65Years - 89Years
All Genders
Healthy Volunteers
NCT05818787

Effect of Vestibular Perceptual Learning on Vestibular Thresholds and Balance

Led by Ohio State University · Updated on 2025-09-11

30

Participants Needed

1

Research Sites

89 weeks

Total Duration

On this page

Sponsors

O

Ohio State University

Lead Sponsor

N

National Institute on Aging (NIA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The intervention being studied is a minimal risk perceptual learning protocol delivered in an academic laboratory setting; the goal of the intervention is to improve the perception of passive whole-body tilts and/or translations, as well as balance, by providing feedback following passive tilts or translations of the body. The protocol lasts a total of \~45 days: Day 1 includes a pre-test assessment of perception and balance, as well as 100 repetitions of training, Days 2-7 each include 400 repetitions of training, and Day 6 includes only post-test assessments of perception and balance.

CONDITIONS

Official Title

Effect of Vestibular Perceptual Learning on Vestibular Thresholds and Balance

Who Can Participate

Age: 65Years - 89Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Must be able to stand
  • No leg or foot amputations
  • No lower limb braces
  • Not currently feeling dizzy or lightheaded
  • Not currently pregnant by self-report
  • Weight 275 pounds or less
Not Eligible

You will not qualify if you...

  • Severe head trauma or traumatic brain injury
  • Any vestibular disorder (e.g., Meniere's Disease, Vestibular Migraine, unresolved BPPV, vestibular hypofunction except due to aging, PPPD)
  • History of seizures
  • Neurologic illness or condition impacting vestibular or balance function (e.g., stroke, neurodegenerative disorders, demyelinating illness)
  • Major psychiatric disorders (e.g., panic disorder, psychosis)
  • Eye diseases or conditions limiting vision worse than 20/40 (e.g., amblyopia, macular degeneration, retina dystrophy, glaucoma, cataracts)
  • Recent (less than 6 months) lower extremity orthopedic injuries
  • Upper extremity injuries requiring current sling immobilization
  • Recent surgery
  • Any other severe health problem (heart disease, pulmonary disease, cancer)
  • Vision in both eyes must be better than 20/40 with best correction
  • Pregnant women
  • Additional exclusion criteria as needed by investigators

AI-Screening

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Trial Site Locations

Total: 1 location

1

The Ohio State University Wexner Medical Center

Columbus, Ohio, United States, 43212

Actively Recruiting

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Research Team

D

Daniel M Merfeld, PhD

CONTACT

S

Shauntelle A Cannon, AuD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

6

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