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Brain Injuries clinical trials

View clinical trials related to Brain Injuries.

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NCT ID: NCT00714571 Completed - Clinical trials for Mild Cognitive Impairment

Behavioral and Neuroimaging Changes After Cognitive Rehab in Traumatic Brain Injuries (TBI) and Mild Cognitive Impairment (MCI)

Start date: July 2008
Phase: Phase 1
Study type: Interventional

Memory deficits are common after traumatic brain injuries (TBI) and are characteristic of various forms of dementia, such as Alzheimer's disease and its common precursor mild cognitive impairment (MCI). This project intends to assess the efficacy of cognitive rehabilitation in these patient populations. We will also use neuroimaging (functional magnetic resonance imaging - fMRI) to assess changes in brain activity that occur following cognitive rehabilitation.

NCT ID: NCT00714428 Completed - Clinical trials for Traumatic Brain Injury

Development of Quality of Life Tool for TBI

TBIQOL
Start date: April 2009
Phase: N/A
Study type: Observational

Objectives: The ultimate goal of this research program is to promote seamless, comprehensive care for Operation Enduring Freedom/ Operation Iraqi Freedom (OEF/OIF) veterans. The purpose of this study is to develop a psychometrically sound tool to measure health-related quality of life (HRQOL) applicable to wounded warriors with TBI (deployment-related TBI).

NCT ID: NCT00704379 Completed - Clinical trials for Traumatic Brain Injury

Treatment Strategy to Prevent Mood Disorders Following Traumatic Brain Injury

Start date: June 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to examine the efficacy of sertraline to prevent the onset of mood and anxiety disorders during the first six months after traumatic brain injury.

NCT ID: NCT00704067 Completed - Clinical trials for Traumatic Brain Injury

Improving Work Outcomes for Veterans With Traumatic Brain Injury

Start date: September 2008
Phase: N/A
Study type: Interventional

The 12-month study will investigate a cognitive training augmentation of supported employment to improve cognitive performance and work outcomes, which are expected to result in improved quality of life and community integration for veterans with mild to moderate traumatic brain injuries. The primary hypothesis is that compared to veterans who receive enhanced supported employment, those who receive supported employment plus cognitive training will work more weeks during the 12 months.

NCT ID: NCT00703495 Completed - Brain Injuries Clinical Trials

Invasive and Non-Invasive Assessment of Cerebral Oxygenation in Patients With Severe Traumatic Brain Injury (TBI)

Start date: July 2008
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the relationship among regional transcranial oxygen saturation (rSO2), brain tissue oxygen pressure (PbtO2) and cerebral perfusion pressure (CPP) in patients with severe traumatic brain injury (TBI).

NCT ID: NCT00702637 Completed - Fatigue Clinical Trials

Study of Modafinil to Treat Fatigue in Persons With Traumatic Brain Injury

Start date: October 2002
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether Modafinil is effective in: (1) reducing fatigue and excessive daytime sleepiness (EDS) in individuals with Traumatic Brain Injury (TBI); and (2) improving cognitive function and quality of life in individuals with TBI.

NCT ID: NCT00702364 Completed - Clinical trials for Traumatic Brain INjury

Efficacy Study of Strattera for Treating Attention Disorders in Traumatic Brain Injury (TBI)

Start date: January 2008
Phase: N/A
Study type: Interventional

Atomoxetine is the only medication that is currently approved by the FDA for the treatment of attention deficit hyperactivity disorder in adults. It has gained recent interest as an alternative medication for treating attentional problems related to traumatic brain injury (TBI), but it's effectiveness in this population has not been studied. There are a number of advantages of Atomoxetine over traditional neuro-stimulant medications currently used for attentional disorders after traumatic brain injury. This study will use a randomized double-blind placebo-controlled crossover design to investigate the efficacy of atomoxetine to improve attention, behavioral function, and depression in adults with TBI

NCT ID: NCT00693121 Completed - Clinical trials for Traumatic Brain Injury

Amantadine for Treatment of Symptoms of the Post-traumatic Confusional State

Start date: April 2003
Phase: Phase 4
Study type: Interventional

Patients with traumatic brain injury often experience a period of acute confusion that may include agitation as they recover from their injuries. While this confusion generally resolves with time, patients may pose increased risk of injury to themselves or others during this period. Their behavior may also increase stress for family members and interfere with their ability to benefit from rehabilitation therapies. A number of different medications have been used to treat confusion to decrease agitation, decrease risk of injury, and improve participation in rehabilitation therapies. To this point, there has not been a research or scientific basis for knowing which medication is the best for a specific patient. The overall goal of this study is to conduct a scientific investigation to help determine which medication works best to treat confusion. Study hypothesis: Amantadine will reduce the severity and number of symptoms of acute confusion after traumatic brain injury.

NCT ID: NCT00692575 Completed - Brain Injuries Clinical Trials

Telephone Intervention for Caregivers of Persons With Traumatic Brain Injury

Start date: June 2008
Phase: Phase 2
Study type: Interventional

This study seeks to determine if problem-based telephone counseling improves quality of life and emotional well-being for caregivers of persons with moderate to severe traumatic brain injury (TBI).

NCT ID: NCT00676182 Completed - Clinical trials for Traumatic Brain Injury

Telerehabilitation for OIF/OEF Returnees With Combat-Related Traumatic Brain Injury

Start date: July 2008
Phase: N/A
Study type: Observational

The scientific objective of this program is to meet the rehabilitation needs of combat wounded Veterans with mild to moderate Traumatic Brain Injury (TBI) via telerehabilitation and determine the effect of this modality of care on patients' physical health and outcomes including function and community participation. The investigators will also evaluate the benefits and limitations of rehabilitation using telehealth from the Veteran and caregiver perspectives and evaluate the impact of rehabilitation via telehealth on Veterans Administration (VA) healthcare facility use.