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Brain Injuries clinical trials

View clinical trials related to Brain Injuries.

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NCT ID: NCT03515317 Completed - Clinical trials for Traumatic Brain Injury

Effects of Neurofeedback in Cognitive Deficit in Patients With TBI

Start date: April 22, 2018
Phase: N/A
Study type: Interventional

Background: Cognitive impairment is common in patients with traumatic brain injury (TBI) at all levels of severity. Such impairments may affect their ability to return to work and thus increase healthcare costs and the associated economic burdens. Both cognitive rehabilitation and stimulant medications are widely used to manage post-traumatic cognitive impairments; however, previous metaanalyses failed to demonstrate their beneficial effects on cognitive recovery in patients with TBI. Nurses, the first-line healthcare providers, should therefore seek and use an alternative approach for dealing with post-traumatic cognitive deficits. Purpose: To assess the effects of low resolution tomography (LoRETA) Z -score neurofeedback (NF) and theta/beta NF in alleviating cognitive impairments in patients with TBI as well as the possible mechanism through which they provide this alleviation. We hypothesize that adults with TBI receiving LoRETA Z-score NF and theta/beta NF will experience the improvements in cognitive functions while participants in the control group will not.

NCT ID: NCT03512054 Completed - Brain Injuries Clinical Trials

Pilot Study Evaluating the Success (= Safe Decannulation) of a Standardized Tracheotomy Weaning Procedure in Brain-injury's Patients

DECATRAC
Start date: June 20, 2018
Phase: N/A
Study type: Interventional

Tracheotomy weaning and decannulation are one of the important problems in the neurosurgical care unit. Aside from medical, psychological, sociological, economical and ethics problems, tracheotomy increases the duration of the hospital stay and conditions the secondarily future medical care (better re-education after the injury). However, according to investigators practices, that patients who were decannulated with success can go into a secondary care residence more easily. This research will demonstrate that all patients included can be decannulated without risk of a new recannulation in the 96 hours.

NCT ID: NCT03511339 Completed - Clinical trials for Mild Traumatic Brain Injury

Pro-2-Cool Device Clinical Study

Start date: November 4, 2017
Phase: N/A
Study type: Interventional

This study is being conducted to quantify the clinical safety and efficacy of head and neck cooling when applied up to 8 days after mild traumatic brain injury (mTBI) among adolescents participating in sporting activities.

NCT ID: NCT03504709 Completed - Clinical trials for Brain Injuries, Traumatic

REsting and Stimulus-based Paradigms to Detect Organized NetworkS and Predict Emergence of Consciousness

RESPONSE 2
Start date: September 5, 2018
Phase:
Study type: Observational

The aim of this study is to assess the utility of advanced magnetic resonance imaging (MRI) and electroencephalographic (EEG) technologies for predicting functional outcomes in patients with severe traumatic brain injury (TBI).

NCT ID: NCT03498495 Completed - Clinical trials for Brain Injury Traumatic Mild

Web-Based Self-Monitoring Activity-Restriction and Relaxation Training Program for Kids With Mild Traumatic Brain Injury

SMART
Start date: May 12, 2019
Phase: N/A
Study type: Interventional

SMART is an interactive web-based program that will allow youth with mild traumatic brain injuries (mTBI) to monitor their symptoms and receive education on problem-solving and coping strategies. This study will evaluate the effectiveness of SMART as a means of improving symptom-management, coping skills, and general well-being during recovery from mTBI. Half of participants will receive the SMART intervention, while half will receive usual care.

NCT ID: NCT03496545 Completed - Clinical trials for Traumatic Brain Injury

Efficacy of Bromocriptine For Fever Reduction in Acute Neurologic Injury

BFF
Start date: November 30, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the antipyretic effect of bromocriptine in critically-ill patients with acute neurologic injury and fever from infectious and non-infectious etiologies.

NCT ID: NCT03490110 Completed - Stress Clinical Trials

Brain Markers of Improvements in Cognitive Functioning

Start date: October 1, 2017
Phase: N/A
Study type: Interventional

Some of the most common, persistent, and disabling consequences of traumatic brain injury affect an individual's ability to achieve personal goals. Interventions that strengthen abilities such as being able to concentrate, remember, stay calm and overcome challenges, could have far reaching benefits for Veterans. One challenge in rehabilitation is that response to training can be highly variable, and a better understanding of the neural bases for this variability could inform care. This pilot project will test the clinical behavioral effects of a cognitive skill training intervention and explore to what extent changes in markers of the brain's electrical activity (using the non-invasive technique of electroencephalograms, EEG) can explain differences in responses to skill training.

NCT ID: NCT03485781 Completed - Cardiac Arrest Clinical Trials

Propofol-induced EEG Changes in Hypoxic Brain Injury

PROPEA3
Start date: October 12, 2017
Phase:
Study type: Observational

PROPEA3 is a prospective observational study investigating the recovery of propofol-induced EEG slow-wave activity and its association with neurological outcome after cardiac arrest.

NCT ID: NCT03480880 Completed - Clinical trials for Traumatic Brain Injury

Bispectral Index Value Changes During Induction and Surgical Decompression in Head Injury Patients

Start date: October 1, 2016
Phase: Phase 4
Study type: Interventional

This study was conducted in two parts: 1. This first part was designed to determine thiopentone dose requirement for induction of anaesthesia with and without the use of Bispectral Index monitoring - Participant and Care Provider in appropriate study arm blinded. 2. As a secondary outcome, Bispectral index monitoring was used to observe changes in neuronal function in intraoperative period as well as haemodynamic changes intraoperatively - Participant and Care Provider blinded.

NCT ID: NCT03479606 Completed - Clinical trials for Traumatic Brain Injury

Online Emotion Regulation Group Intervention

Start date: April 5, 2018
Phase: N/A
Study type: Interventional

This study will examine the efficacy of an emotion regulation intervention delivered online to individuals with traumatic brain injury (TBI) with deficits in emotion regulation. 104 subjects will be enrolled and will receive 24, 60-minute emotion regulation skills-training sessions twice a week for 12 weeks, delivered online in a group video-conference with 3-5 other participants. Participants will be asked to complete online surveys, lasting approximately 40-50 minutes, every four weeks during the intervention and the 12-week follow-up phase. Attendance and compliance will be tracked, and outcomes will be monitored using online data collection methods.