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Traumatic Brain Injury clinical trials

View clinical trials related to Traumatic Brain Injury.

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NCT ID: NCT01794585 Completed - Clinical trials for Traumatic Brain Injury

Virtual Reality (VR) Treatment for Balance Problems in Traumatic Brain Injury (TBI)

Start date: April 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effectivenes of a home-based physical therapy program designed to improve balance following traumatic brain injury by incorporating the use of a virtual reality system.

NCT ID: NCT01789164 Completed - Clinical trials for Traumatic Brain Injury

Measure of Cerebrovascular Dysfunction After TBI With fNIRS

Start date: January 2013
Phase:
Study type: Observational

The goal of this project is to determine if it is possible to assess Cerebrovascular Reactivity (CVR) to hypercapnia with functional Near Infrared Spectroscopy (fNIRS). Such a method would be particularly helpful in traumatic brain injury (TBI), where objective measures are needed, and would greatly expand the capacity to make such assessments in standard clinical practice.

NCT ID: NCT01768650 Completed - Chronic Pain Clinical Trials

Structured Treatment of Pain (STOP) Study

STOP
Start date: June 2014
Phase: N/A
Study type: Interventional

This study seeks to compare two different behavioral treatments for pain in Veterans with a history of TBI. Both treatments involve educating the Veteran about pain, discussing the impact of pain, and different ways to manage it in hopes of decreasing pain and its impact on life. These approaches are called "self-management" approaches to pain. Both of these treatments are commonly used in pain clinics to treat pain in persons with back pain, headaches, and other types of chronic pain. The investigators will be delivering both treatments over the telephone to make the treatments accessible to Veterans wherever they live.

NCT ID: NCT01763892 Completed - Clinical trials for Traumatic Brain Injury

Physiologic Mechanisms in Pediatric Traumatic Brain Injury (TBI)

Start date: December 2012
Phase: N/A
Study type: Observational

The aims of this study explore the relationships between cerebral vasospasm, apolipoprotein-E (apo-E) genotype, physiologic symptoms, and neurocognitive outcomes that may either intensify or ameliorate secondary injury, for children with a traumatic brain injury. Exploring the apo-E genotype will help us know if injury response is altered in certain children and will aid in developing interventional approaches.

NCT ID: NCT01762475 Completed - Clinical trials for Traumatic Brain Injury

Sildenafil for Cerebrovascular Dysfunction in Chronic Traumatic Brain Injury.

Start date: January 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether sildenafil (Viagra®) is effective in improving cerebral blood flow and cerebrovascular reactivity inpatients who have persistent symptoms at least 6 months after a traumatic brain injury (TBI).

NCT ID: NCT01749735 Completed - Clinical trials for Traumatic Brain Injury

Transcranial Direct Current Stimulation and Motor Training for Traumatic Brain Injury Survivors

tDCS TBI
Start date: July 2011
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effect of transcranial direct current stimulation and functional upper extremity task training to functional upper extremity task task training alone. The functional upper extremity task training takes uses the Armeo Spring robotic arm to support the limb while playing functional task games on the computer. Specific Aims: 1. To demonstrate that tDCS combined with upper extremity functional task training in a virtual environment is more effective than functional task training in a virtual environment with sham tDCS. 2. To compare cortico-excitatory changes following training with tDCS vs. sham stimulation, using paired- and single-pulse transcranial magnetic stimulation as a tool to measure cortical excitability.

NCT ID: NCT01745146 Completed - Clinical trials for Traumatic Brain Injury

Anger Self-Management in Traumatic Brain Injury

ASMT
Start date: September 2012
Phase: N/A
Study type: Interventional

The present study addresses problematic anger and irritability in community dwelling persons with traumatic brain injury (TBI). It is designed to test the worth of a novel treatment approach called Anger Self-Management Training (ASMT), compared to a treatment offering supportive therapy focused on personal readjustment and education, the PRE (Personal Readjustment and Education). The project is a 3-center randomized controlled trial employing equivalent therapist time and therapeutic structure in the delivery of treatment options. The overall aim is to evaluate the relative response rate and correlates of treatment response for the ASMT as compared to the PRE.

NCT ID: NCT01730261 Completed - Clinical trials for Traumatic Brain Injury

Online Emotional Regulation Group Treatment

Start date: November 2012
Phase: Phase 1
Study type: Interventional

This study will examine the feasibility of online delivery of emotional regulation training to individuals with TBI with emotional dysregulation. 80 subjects with significant emotional dysregulation will be enrolled and will receive 24 60-minute emotional regulation sessions twice a week for 12 weeks, delivered online in group modality. Attendance and compliance will be tracked, and outcomes will be monitored using online data collection methods. Treatment satisfaction and participant subjective experience will also be assessed.

NCT ID: NCT01728350 Completed - Clinical trials for Traumatic Brain Injury

Improving Well-Being After TBI Through Structured Volunteer Activity

Start date: April 2013
Phase: N/A
Study type: Interventional

The purpose of this project is to determine if participating in volunteer activity improves the psychological well-being of individuals with traumatic brain injury (TBI).

NCT ID: NCT01728142 Completed - Clinical trials for Traumatic Brain Injury

Comparison of the DANA to the ANAM in the Evaluation of Cognitive Changes After Concussion

Start date: January 2013
Phase: N/A
Study type: Interventional

The Defense Automated Neurobehavioral Assessment (DANA) was recently developed as a durable, portable, and "field-hardened" NeuroCognitive Assessment Tool. The purpose of this study is to compare the sensitivity of the DANA Brief exam with the Automated Neuropsychological Assessment Metrics (ANAM) battery currently used by the military after concussion. The primary hypothesis is that the DANA Brief exam will be more sensitive for detecting continued impaired cognitive performance than the ANAM during recovery after a concussion.