The Use of the PoNS™ Device in the Treatment of Blunt and Blast Induced Vestibular Disorders
Traumatic brain injury (TBI) is a major worldwide health issue. Figures from the Centers for Disease control show that 1.7 million people suffer a TBI annually. Meanwhile the World Health Organization recognizes TBI as one of the most significant health issues in developing countries. In the military, mild traumatic brain injury (mTBI) is one of the most frequent sequela of modern war. Dizziness and balance disorders are the most frequent sequela of mTBI and account for a significant degree of mTBI morbidity. At the current time, the best treatment modality for dizziness secondary to mTBI is vestibular rehabilitation (VR). While VR is effective, the therapy is time consuming, not universally successful, and results in incomplete recovery by many patients. Work needs to be done in an attempt to improve therapy outcomes. This project will study the use of neuromodulation (through stimulation of the tongue) as an adjuvant to improve the effectiveness of VR and reduce the time involved in VR. Given past work with variants on this minimal medical impact appliance, using the PoNS™ device to augment therapy may result in a significant improvement in VR outcomes. Given the enormous public health and military burden of mTBI, and given that dizziness is a major component often responsible for significant morbidity, this project has significant military and civilian impact and can be beneficial to those who suffer mTBI worldwide.
|Study Design:||Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Treatment
|Official Title:||The Use of the PoNS™ Device in the Treatment of Blunt and Blast Induced Vestibular Disorders|
- Change in Sensory Organization Test score [ Time Frame: Change from Baseline SOT score at 3 months ] [ Designated as safety issue: No ]Posturography for Sensory Organization Test: Utilizing a computerized dynamic posturography (Neurocom Inc., Clackmas, OR) the sensory organization test (SOT) is conducted by measuring postural sway on a force plate under six different conditions as follows 1) Normal Stance eyes open, 2) Normal Stance with eyes closed, 3) Normal Stance with sway referenced visual surround, 4) Sway reference stance eyes open, 5) Sway reference stance with eyes closed, and 6) Sway reference stance with sway referenced vision. The SOT will conduct three trials in each condition and utilize the information to produce a computer generated objective score of balance/posture function. The exam takes less than ten minutes to produce.
- Change in Vestibular-Ocular Reflex scores [ Time Frame: Change from Baseline VOR score at 3 months ] [ Designated as safety issue: No ]VOR Tests: A Neuro Kinetics IPortal Video-oculography system (Neurokinetics Inc., Pittsburgh, PA) with a six degree of freedom accelerometer will be used to (1) document head thrust test findings qualitatively and (2) provide objective measurements of test results. The software will be configured for (1) detection of head thrusts of appropriate direction and orientation (re: earth vertical) and (2) real-time determination of performance parameters (VOR).
- Change in Functional Gait Assessment Test scores [ Time Frame: Change from Baseline FGAT score at 3 months ] [ Designated as safety issue: No ]The Functional Gait Assessment Test (FGAT) is a 10 item gait task test in which each task is graded on a 0-3 scale with 0 indicating could not perform and 3 indicating performed without error. Grading is done by an experienced rater. The FGAT produces an ordinal score on a 0-30 point scale and is normed from previous civilian and military studies.
- Change in Dizziness Handicap Index scores [ Time Frame: Change from Baseline DHI score at 3 months ] [ Designated as safety issue: No ]The Dizziness Handicap Index (DHI) is a well-validated self report the produces a score on a hundred-point scale.
- Change in Activities specific Balance Confidence scale scores [ Time Frame: Change from Baseline ABC score at 3 months ] [ Designated as safety issue: No ]The Activities specific Balance Confidence scale (ABC) is a 16 question survey in which individuals' answer how confident they are about being able to perform a balance related task on a 0%-100% scale. The questionnaire is scored by adding the percentages and dividing by 100% to arrive at a scaled score form 0-100.
|Study Start Date:||February 2013|
|Estimated Study Completion Date:||January 2016|
|Estimated Primary Completion Date:||June 2015 (Final data collection date for primary outcome measure)|
Experimental: Treatment Arm
Device: PoNS™ device
The PoNS™ device uses electrotactile waveform in conjunction with the Cranial Nerve - Non-Invasive NeuroModulation (CN-NINM) intervention. This involves using both balance and gait training methods to stabilize symptoms, regain balance & gait, and affect the functional transfer of improved stability and mobility to activities of daily living. It is based on a body of work focused on developing the tongue-based human-machine interface and application of this technology for balance, vision, and auditory substitution and more recently as neuromodulation for brain rehabilitation after injury and disease.
Other Name: Portable Neuromodulation Stimulator, version 2.2
Placebo Comparator: Placebo Arm
Other: Placebo device
Please refer to this study by its ClinicalTrials.gov identifier: NCT01771575
|Contact: Sara A Murphy, MPHemail@example.com|
|United States, California|
|Naval Medical Center, San Diego||Not yet recruiting|
|San Diego, California, United States, 92134|
|Contact: Sara A Murphy, MPH 619-532-6820 firstname.lastname@example.org|
|Principal Investigator: Michael E. Hoffer, M.D.|
|Principal Investigator:||Michael E. Hoffer, M.D.||United States Naval Medical Center, San Diego|