Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Middleton, Wisconsin 53562


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.

Study summary:

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.


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.



Primary Contact:

Principal Investigator
Mary Beth Badke, PT, PhD
University of Wisconsin, Madison

Backup Contact:


Location Contact:

Middleton, Wisconsin 53562
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: June 25, 2018

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.

Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.