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Vestibular Stimulation to Treat Hemispatial Neglect

Noise Enhanced Galvanic Vestibular Stimulation in Hemispatial Neglect

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00271388
Enrollment
2
Registered
2005-12-30
Start date
2006-01-31
Completion date
2008-12-31
Last updated
2018-06-06

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

Conditions

Hemispatial Neglect, Stroke

Keywords

Galvanic Vestibular Stimulation, Hemispatial Neglect, Stroke

Brief summary

The purpose of the current proposal is to pilot a new and potentially improved treatment for neglect. The procedure involves the delivery of transcutaneous small-amplitude current to the vestibular nerves that lie directly below the mastoid bones.

Detailed description

The purpose of the current proposal is to pilot a new and potentially improved treatment for neglect. The procedure involves the delivery of transcutaneous small-amplitude current to the vestibular nerves that lie directly below the mastoid bones. With the intention of boosting activity in the damaged left hemisphere, positive and negative current is delivered to the left and right mastoids respectively. While successfully used to rehabilitate gait and balance disorders, the procedure has only once been applied to neglect. In the present investigation, we will first confirm and then optimize the conditions under which galvanic vestibular stimulation (GVS) ameliorates neglect. This in turn will justify subsequent work (in a later funding cycle) that will demonstrate the safety and efficacy of the treatment on a much larger clinical scale, and merit the construction of a miniaturized portable device.

Interventions

DEVICETranscutaneous current to the vestibular nerve

Delivery of randomly oscillating low level current

Sponsors

VA Office of Research and Development
Lead SponsorFED

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
40 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* All participants must be literate in English * Right handed * Have corrected near-visual acuity of 20/40 or better * Patients must also have a minimum of twelve years education * These inclusionary criteria are based on the data of both Black, Yu, Martin, and Szalai (90) and our own studies. * They are intended to assure that only patients with sufficiently severe symptoms will be admitted to our study.

Exclusion criteria

Exclusionary criteria include: * Homonymous hemianopia * Presence of a severe field cut extending toward the midline on formal perimetry (however many patients who have field cuts restricted to the periphery will be able to fully perceive our stimulus displays so can be included * Evidence of aphasia on clinical examination (crossed aphasia) * A significant history of other neurological or psychiatric illness or drug/alcohol abuse

Design outcomes

Primary

MeasureTime frameDescription
Measures of Hemispatial Neglect30 daysImprovement of Hemispatial neglect

Countries

United States

Outcome results

None listed

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