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OpenTrials
Completed

NCT Number: NCT00567944

Use of the BrainPort® Balance Device to Improve Balance in Adults With Balance Deficits Due to Stroke

The purpose of this study is to evaluate the safety and efficacy of the BrainPort balance device in improving balance in people with balance deficits due to stroke.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Wisconsin-Madison

Middleton, Wisconsin, 53562, United States

About this study

Following baseline assessments, subjects participate in 5 consecutive days (10 hours) of clinic training with the BrainPort balance device with a Physical Therapist. Assessments are repeated at the end of clinic training. Following clinic training, subjects take the device home to use for two (2) 20 minute training sessions each day. Subjects return to the clinic for one (1) day of testing after using the device at home for 7 weeks.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • At least 18 years old.
  • Diagnosis of stroke for at least 6 months.
  • Reached a plateau and been discharged from physical therapy.
  • Able to ambulate with or without assistance.
  • Ongoing balance problem.
  • Able to read and understand the informed consent form, and willing to sign the informed consent form.

Exclusion criteria

  • Current oral health problems as determined by health questionnaire and an examination of the oral cavity.
  • Any medical condition that would interfere with performance on the assessments.
  • History of seizures.
  • Pregnancy.
  • Cognitive deficits (Mini-Mental 25 or below), joint replacements, cervical vertigo, or major neurologic disease, major depression or disabling psychiatric disorder.
  • Known neuropathies of tongue or skin tactile system.
  • Prior exposure to BrainPort® balance device.
  • Subjects who are unwilling or unable to adhere to all study requirements, including completion of the training period, evaluation tests, and return to clinic for a follow-up visit.
  • Subjects who have undergone middle ear or other surgery with sacrifice or damage to the chorda tympani nerve, lingual nerve, or hypoglossal nerve.

Treatment and study plan

BrainPort Balance Device

Device

The BrainPort balance device, is a non-invasive medical device that provides head and body position information to a person via their tongue.

Primary outcomes

  1. Dynamic Gait Index

    Time frame: baseline, 5 days, end of study

  2. Berg Balance Scale

    Time frame: Baseline, 5 days, end of study

  3. Activities-specific Balance Confidence Scale

    Time frame: Baseline, 5 days, end of study

  4. Timed Up and Go

    Time frame: Baseline, 5 days, end of study

  5. Stroke Impact Scale

    Time frame: Baseline, 5 day, end of study

Sponsors and collaborators

Lead sponsor

Wicab

Industry

Registry information

Official study title

A Substitute Vestibular Information System Using the BrainPort® Balance Device for Adults With Chronic Vestibular Dysfunction Following Stroke

Important dates

Study start
2007
Primary completion
2010
Study completion
2010
First posted
Dec 5, 2007
Registry last updated
Jun 28, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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