Trials / Terminated
TerminatedNCT01749800
Galvanic Vestibular Stimulation and Motor Training in Traumatic Brain Injury Survivors
Combining Galvanic Vestibular Stimulation and Motor Training in Traumatic Brain Injury Survivors With Attentional Deficits
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 7 (actual)
- Sponsor
- Spaulding Rehabilitation Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The overall goal of the proposed project is to perform a preliminary study to assess the potential effects of galvanic vestibular stimulation (GVS) on the outcomes of a cognitive test of attention and the outcomes of robot-assisted upper-limb rehabilitation.
Detailed description
We plan to explore the use of GVS on the severity of attention span deficits and motor training delivered using a spring-based robot. We intend to carry out the study in a small cohort of traumatic brain injury (TBI) survivors (20 subjects). Subjects with attention span deficits but no significant motor impairments will solely undergo a cognitive test of attention with/without GVS. Subjects with both attention span deficits and significant motor impairments will undergo a cognitive test of attention and robot-assisted upper-limb rehabilitation with/without GVS.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | GVS | A small current is delivered to the vestibular system via electrodes placed over the subject's mastoid processes. |
| DEVICE | Sham GVS | Electrodes are placed over the subject's mastoid processes and connected to the device, but the device is not active. |
| DEVICE | Armeo Spring | A robotic system supports the weak arm of the subject to make it easier to perform therapeutic exercises. |
Timeline
- Start date
- 2011-07-01
- Primary completion
- 2014-11-01
- Completion
- 2014-11-01
- First posted
- 2012-12-17
- Last updated
- 2017-05-31
- Results posted
- 2017-05-31
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01749800. Inclusion in this directory is not an endorsement.