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protocol withdrawn
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| Name | Class |
|---|---|
| Virginia Commonwealth University | OTHER |
| US Department of Veterans Affairs | FED |
| The Defense and Veterans Brain Injury Center | FED |
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The purpose of this study is to determine the feasibility of combining PoNS therapy with standard vestibular and balance therapy with the proposed double-blind design; evaluate preliminary indications of efficacy. This study is also evaluating recruitment rate, completion rate, device usability, and outcome measures feasibility.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Active CN-NINM PoNS | Experimental | Active CN-NINM PoNS - Active cranial-nerve non-invasive neuromodulation (CN-NINM) using the Portable Neuromodulation Stimulator (PoNS) and balance/gait rehabilitation with physical therapy |
|
| Sham PoNS CN-NINM | Placebo Comparator | Sham CN-NINM PoNS - Sham cranial-nerve non-invasive neuromodulation (CN-NINM) using the Portable Neuromodulation Stimulator (PoNS) and balance/gait rehabilitation with physical therapy |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Active CN-NINM PoNS | Device | Delivery of active stimulation of the tongue during in-person therapy sessions (1 hour) and during two home sessions (40 minutes) daily on 6 of 7 days per week (120 total sessions). Stimulation sessions will be separated by at least 4 hours. |
| Measure | Description | Time Frame |
|---|---|---|
| Recruitment rate | Number and percentage of subjects recruited over the 36 week pilot recruitment phase | 36 weeks |
| Completion and compliance rates | Number and percentage of subjects who complete the study | Up to 12 weeks |
| Usability rating | Number and percentage of subjects and therapists who rated usability as good or better. | 12 weeks |
| Success of blinding | Number and percentage of subjects who accurately guess group membership | 12 weeks |
| Change in Sensory Organization Test (SOT) | Comparison of the SOT score between the treatment group and sham group at the intermediate follow-up. | 12 weeks |
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Inclusion Criteria:
Exclusion Criteria:
History of traumatic brain injury (TBI) of any severity other than mild TBI
Presence of active substance abuse condition
Any condition for which posturography is contraindicated (e.g. leg amputation or fracture)
Diagnosed neurological disorder with balance sequelae, other than TBI (e.g. Parkinson's disease, incomplete spinal cord injury, or Multiple Sclerosis)
Orthostatic hypotension as defined by:
An implanted medical device
Pregnancy
Oral infection
Known transmissible disease (HIV, hepatitis, influenza, TB)
Exam signs of serious disorder other than mTBI as defined by facial asymmetry, hoarseness and dysarthria (e.g. tumor, stroke).
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| Name | Affiliation | Role |
|---|---|---|
| David X Cifu, MD | VA Department of Physical Medicine and Rehabilitation | Principal Investigator |
| William C Walker, MD | Virginia Commonwealth University (VCU) | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| McGuire Veterans Affairs Medical Center | Richmond | Virginia | 23249 | United States | ||
| Virginia Commonwealth University |
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| Sham CN-NINM PoNS | Device | Delivery of sham stimulation of the tongue during in-person therapy sessions (1 hour) and during two home sessions (40 minutes) daily on 6 of 7 days per week (120 total sessions). Stimulation sessions will be separated by at least 4 hours. |
|
| Richmond |
| Virginia |
| 23298-3038 |
| United States |
| ID | Term |
|---|---|
| D001924 | Brain Concussion |
| ID | Term |
|---|---|
| D000070642 | Brain Injuries, Traumatic |
| D001930 | Brain Injuries |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D006259 | Craniocerebral Trauma |
| D020196 | Trauma, Nervous System |
| D016489 | Head Injuries, Closed |
| D014947 | Wounds and Injuries |
| D014949 | Wounds, Nonpenetrating |
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