Clinical Trials Directory

Trials / Completed

CompletedNCT00567944

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

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
29 (actual)
Sponsor
Wicab · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

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.

Conditions

Interventions

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

Timeline

Start date
2007-06-01
Primary completion
2010-04-01
Completion
2010-04-01
First posted
2007-12-05
Last updated
2012-06-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00567944. Inclusion in this directory is not an endorsement.