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Brain Injuries, Traumatic clinical trials

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NCT ID: NCT03608722 Active, not recruiting - Dementia Clinical Trials

Video Games to Track Cognitive Health

Start date: November 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to assess cognitive function using a rapid, portable, computerized neurocognitive testing device in a wide variety of clinical settings.

NCT ID: NCT03605017 Recruiting - Clinical trials for TBI (Traumatic Brain Injury)

The Development of a Virtual Reality Program to Improve Attention in Individuals With TBI

Start date: March 26, 2014
Phase: N/A
Study type: Interventional

The purpose of this research is to investigate the effectiveness of a technique designed to improve divided attention and set-shifting impairments in persons with a traumatic brain injury (TBI). The study is designed to evaluate how well this technique can help people with TBI increase their attention and ability to function better in everyday life.

NCT ID: NCT03600324 Active, not recruiting - Clinical trials for Mild Traumatic Brain Injury

Randomized Controlled Trial for Vestibular Treatment in Concussion

Start date: February 26, 2020
Phase: N/A
Study type: Interventional

A prospective, single-blind, four-group multi-center randomized controlled trial (RCT) of targeted rehabilitation exercises for vestibular symptoms and impairments (T-REV) in civilians with mild traumatic brain injury (mTBI) will be conducted at the University of Pittsburgh Medical Center Sports Medicine Concussion Program (UPitt). The four treatment groups will consist of the factorial combinations of low (30%) and high (70%) intensity of exercise crossed with low (12-18 min, 1x/day) and high (12-18 min, 2x/day) frequency. A total of 125 participants aged 18-50 years will be enrolled across years 1-4, with approximately 100 participants completing the whole study. After potential participants with mTBI are screened for the vestibular clinical profile, using domain-specific tests and measures, and enrolled into the study, participants will complete primary and secondary outcome measures and receive a home exercise program that a) targets participants individual deficits, and b) is of the appropriate intensity and frequency for the participant's randomly assigned treatment group. Participants will return for in-clinic visits once per week to receive treatment and progress assigned exercises.

NCT ID: NCT03597763 Completed - Clinical trials for Traumatic Brain Injury

Fatigue Following Moderate and Severe TBI

Start date: March 1, 2018
Phase:
Study type: Observational

The subjective feeling of being periodically fatigued, tired, even exhausted is common in the general population, as well as in a large number of medical conditions, including neurological illness, such as traumatic brain injury (TBI), cerebrovascular accidents (CVA), multiple sclerosis (MS), and poliomyelitis. Fatigue typically results in compensatory behaviors such as spending extended time in bed, daytime napping, and restricted participation in activities of daily living, which in turn can have a profound negative impact on mental and physical health. Although fatigue is common and debilitating, there is a scarcity of knowledge concerning underlying biological, psychological and psychosocial mechanisms in the development and maintenance of persisting fatigue. There is also a general lack of theoretical accounts of potentially shared and etiology-specific mechanisms across conditions. The existence of clinical subgroups and diverse clinical trajectories is not well documented, resulting in a lack of evidence-based treatment opportunities. Diagnosis and management of fatigue is further challenged by difficulties in conceptualizing and defining the phenomenon itself, since fatigue is subjectively experienced and multifaceted. Thus, as fatigue often poses a chronic problem, health professionals in community based rehabilitation settings are faced with helping patients cope with this symptom without a clear understanding of causes or treatment options. The current project aims to map the occurrence of fatigue following moderate to severe TBI and achieve a better theoretical and clinical understanding of the mechanisms which may cause, exacerbate or protect against persisting fatigue following TBI. The study approach acknowledges that fatigue after neurological illness is the result of complex interplays between general individual predispositions and etiology-specific factors. A better understanding of these mechanisms is a prerequisite for personalized treatment and development of empirically based randomized controlled intervention studies. This approach has relevance to other clinical conditions as well. The long-term aim is to ensure accurate diagnosis, improve treatment and rehabilitation, and to contribute to knowledge based clinical decision-making both within specialized and community based rehabilitation settings.

NCT ID: NCT03594734 Active, not recruiting - Clinical trials for Traumatic Brain Injury

Group Lifestyle Balanceā„¢ for Individuals With Traumatic Brain Injury (GLB-TBI)

Start date: January 8, 2019
Phase: N/A
Study type: Interventional

The purpose of this RCT is to examine the efficacy of a Group Lifestyle Balanceā„¢ (GLB) program adapted for people with traumatic brain injury (TBI) on primary (weight) and secondary outcomes at 3, 6, 12, and 18 months from enrollment into the program.

NCT ID: NCT03582579 Active, not recruiting - Clinical trials for Mild Traumatic Brain Injury

Enhancing Brain Training With Virtual Reality

Start date: June 27, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of brain training in a Virtual Reality set up in neurotypical populations as well as in the traumatic brain injury population.

NCT ID: NCT03582228 Completed - Clinical trials for Traumatic Brain Injury

Bridging Recovery Allies in Virtual Environments

BRAVE
Start date: August 6, 2018
Phase: N/A
Study type: Interventional

The Bridging Recovery Allies in Virtual Environments (BRAVE) study aims to evaluate the acceptability and feasibility of implementing a virtual environment (VE) social support group for social communication training among adults with traumatic brain injury (TBI).

NCT ID: NCT03578003 Recruiting - Clinical trials for Post-traumatic Stress Disorder

Morning Bright Light to Improve Sleep Quality in Veterans

Start date: August 2, 2017
Phase: N/A
Study type: Interventional

One of the principal complicating factors associated with traumatic brain injury (TBI) is sleep-wake disturbances (e.g., insomnia, excessive daytime sleepiness, and circadian rhythm sleep disorders). Morning bright light therapy (MBLT) has been shown to improve sleep quality in a variety of conditions, but little has been done investigating the utility of MBLT in improving sleep in Veterans with TBI. This proposal aims to determine the effect of MBLT on sleep quality in Veterans with TBI. Veterans with and without TBI will be recruited from the VA Portland Health Care System. Baseline questionnaires and 7 days of actigraphy will be collected prior to engaging in 60 minutes of MBLT daily for 4 weeks, during which actigraphy will also be collected continuously. Post-MBLT questionnaire data will be collected, and follow-up questionnaire data will be collected at 3 months post-MBLT.

NCT ID: NCT03575169 Completed - Clinical trials for Traumatic Brain Injury

The Use of Bispectral Index Monitoring to Assess Depth of Sedation in Patients With Traumatic Brain Injury

BIS-TBI
Start date: July 1, 2019
Phase:
Study type: Observational

An observational study to assess the BIS reported level of sedation of patients with traumatic brain injury in the ICU.

NCT ID: NCT03566368 Completed - Clinical trials for Cardiac Complication

Cardiac Dysfunction in Traumatic Brain Injury

Start date: December 5, 2015
Phase:
Study type: Observational

Patients with Head Injury have been associated with varying degree of cardiac dysfunction resulting in adverse events during emergency surgery and during recover from head injury. This study intends to study the incidence and impact of cardiac dysfunction using electrocardiogram, transthoracic echocardiogram and cardiac enzyme levels in head injury patients during and following emergency surgery. Our results will facilitate better management, guide specific therapy and help in prognostication in this group of patients.