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OKS for Gait Instability

Optokinetic Stimulation for the Treatment of Gait Abnormalities

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03579186
Enrollment
0
Registered
2018-07-06
Start date
2015-06-19
Completion date
2022-12-12
Last updated
2022-12-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gait, Unsteady, Vestibular Disorder

Brief summary

Specific aim: To determine whether optokinetic stimulation can improve gait abnormalities. Hypothesis: Optokinetic stimulation stimulates the vestibular system and can improve vestibular induced gait disorders.

Detailed description

This is a pilot study designed to determine whether or not the optokinetic stimulation improves gait in patients with gait abnormalities, specifically vestibular induced gait disorders. The study population will consist of patients already receiving a gait assessment through the Brain Fit Club (BFC) at Beth Israel Deaconess Medical Center. This gait assessment involves walking and posture evaluations. Patients will complete a gait assessment as part of their normal BFC evaluation. Those who consent to participate in the study will then complete a gait assessment while receiving optokinetic stimulation. The investigators will compare baseline gait and postural control before and during OKS stimulation.

Interventions

DEVICEOKS

Optokinetic stimulation

Sponsors

Beth Israel Deaconess Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
NONE

Intervention model description

Patients undergoing a clinical gait assessment will be recruited for this study. Those that consent to participate will complete their clinical gait assessment as part of their normal evaluation. Subjects will then complete a gait assessment while wearing experiencing optokinetic stimulation. The investigators will compare baseline gait and postural control before and during OKS stimulation.

Eligibility

Sex/Gender
ALL
Age
50 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Receiving a gait assessment through the BFC * Ages 21-75

Exclusion criteria

* Left hemiparesis * Requires a cane or walker * Documented evidence of falls or instability to the left * Reduced vision * Moderate or severe dementia

Design outcomes

Primary

MeasureTime frameDescription
Gait - (measured using a wireless 3D accelerometer)After 5 minutes of OKSChange in walking balance (lateral step deviation) as measured using a wireless 3D accelerometer
Posture - (measured using a stationary force platform)After 5 minutes of OKSChange in standing balance (left-right deviation) as measured using a stationary force platform.

Secondary

MeasureTime frameDescription
SpeedAfter 5 minutes of OKSChange in gait speed

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026