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Stroke clinical trials

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NCT ID: NCT03619642 Completed - Stroke Clinical Trials

Reliability, Validity and Clinical Utility of a Robotic Assessment for Proprioception

Start date: December 15, 2017
Phase: N/A
Study type: Interventional

The aim of this case-controlled observational cross-sectional study is to investigate the test-retest reliability, validity and clinical utility of a rapid robotic assessment of finger proprioception using a passive gauge position matching tasks in MS and stroke subjects. Session 1 Informed consent Descriptive measures Session 2 Clinical testing Robotic assessment (3x) Session 3 Clinical testing Robotic assessment (3x)

NCT ID: NCT03618732 Completed - Stroke Clinical Trials

A Randomized Controlled Trial of Bilateral Movement-based Computer Games Training to Improve Motor Function of Upper Limb and Quality of Life in Sub-acute Stroke Patient

Start date: August 3, 2015
Phase: N/A
Study type: Interventional

This study aims at investigating whether bilateral movement-based training with computer games could augment motor function of paretic upper limb and improve quality of life in sub-acute stroke patients.

NCT ID: NCT03618290 Completed - Stroke, Acute Clinical Trials

Plasma Free Fatty Acids Profile As A Diagnostic Tool For Acute Ischemic Stroke

Start date: September 19, 2018
Phase:
Study type: Observational

The purpose of the research is to use plasma free fatty acid profiling as a biomarker for ischemic stroke. The plasma free acid profile will be specifically and significantly changed in early stages upon stroke onset, and correlate with the stroke volume and progression determined by imaging techniques.

NCT ID: NCT03618251 Completed - Clinical trials for Stroke, Software Verification, Diffusion Weighted MRI, Neuroimaging

Automated Volume Assessment of Acute Stroke

AVAAS
Start date: March 15, 2018
Phase:
Study type: Observational

Stroke is a common disease. It is increasingly managed in non-specialized centers. The volume of the lesion, evaluated on the diffusion weighted imaging, is a prognostic factor of clinical progression and is useful for the treatment decision. There is therefore a real interest in having a reliable software able to detect the stroke and evaluate the volume of the cerebral infarction. The aim is to provide rapid information to the interventional neuroradiologist and optimize the care of the patient. The Alberta Stroke Program Early Computed Tomography Score currently used to predict response to treatment divides the territory of the middle cerebral artery. It has a few limitations, it is unreproducible and concerns only the territory of the middle cerebral artery. Manual volumetry is a long and also not very reproducible technique. The aim of our study is to evaluate the reproducibility and diagnostic performances of the automated segmentation software based on the diffusion weighted imaging sequence, and to compare it to manual and semi-automatic measurements.

NCT ID: NCT03618069 Not yet recruiting - Stroke Clinical Trials

Diagnosis by Comprehensive Cardiovascular Imaging for Stroke and TIA

DCCIST
Start date: September 1, 2018
Phase: N/A
Study type: Interventional

Stroke affects over 125,000 people each year in the UK and leaves at least 50% disabled. After a first stroke, there is a significant risk of recurrence (around 5-10% over the first year). While there are benefits from addressing general risk factors such as exercise, weight and smoking, selecting the best treatments for preventing a further stroke depends on understanding the underlying mechanism. Most strokes results from a blood clot causing a blockage in a blood vessel in the brain ("ischaemic" strokes, about 85% of cases). The clot may originate in the heart, the major blood vessels supplying the head, or result from disease of the small blood vessels in the brain itself (around 25% of cases each), and in around 25% of people a cause cannot be determined (sometimes because more than one exists). Different treatments are given depending on cause (for example, anticoagulant medication for clots from the heart, surgery for some arising from large arteries in the neck). Current investigations involve multiple tests spread across different hospital departments, and commonly take several weeks to be completed. This may contribute to a high rate of strokes of uncertain cause, and may delay the start of the best treatment. This trial will investigate the value of a single comprehensive scan to look at the heart and major blood vessels (using CT scanning) in a pilot study, comparing the classification of causes of stroke and the time to starting treatments with routine care, in a randomised study of patients with recent stroke or transient ischaemic attack (TIA, a short-lived stroke episode).

NCT ID: NCT03617159 Not yet recruiting - Clinical trials for Pediatric Cerebral Stroke

Role of Advanced Magnetic Resonance Imaging in Assessment of Pediatric Cerebral Stroke

Start date: October 2018
Phase:
Study type: Observational

Stroke can be ischemic, hemorrhagic, or both. Early recognition and treatment of pediatric stroke are critical in optimizing long-term functional outcomes, reducing morbidity and mortality, and preventing recurrent stroke. Neuroimaging plays a vital role in achieving this goal. Neuroimaging is usually the first step in diagnosis, helping discriminate between ischemic/hemorrhagic strokes and also in the identification of underlying potential causes. Multiparametric magnetic resonance imaging (MRI) plays a crucial role in assessing pediatric cerebral stroke including diffusion-weighted imaging (DWI), susceptibility weighted imaging (SWI) and magnetic resonance angiography (MRA).

NCT ID: NCT03615079 Completed - Stroke Clinical Trials

Internet-based CBT After Stroke Pilot

iSAD
Start date: June 11, 2018
Phase: N/A
Study type: Interventional

Mood disorders occur in 25-30% of stroke patients and are associated with lower quality of life, higher mortality, increased healthcare utilization, and higher costs. Cognitive behavioral therapy (CBT) interventions have been shown to both treat and prevent post-stroke mood disorders, thus having the ability to improve quality of life and reduce costs. This study aims to test the feasibility of internet-based CBT combined with a telephone/email based coaching service after stroke.

NCT ID: NCT03614585 Recruiting - Stroke Clinical Trials

Exercise Intensity Matters in Stroke Rehabilitation

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

The main objective of this multi-site project is to compare the effects of 12 weeks of HIIT vs. MICT on brain plasticity. The effects of HIIT vs. MICT on cardiovascular health, psychosocial predictors of physical activity and motor function will also be compared. HIIT and MICT will be delivered through a whole-body exercise paradigm using a recumbent stepper that requires arm and leg forces. Outcomes will be assessed at baseline (T0, 0 weeks), at the end of the intervention (T1, 12 weeks) and at 8-week follow-up (T2, 20 weeks).

NCT ID: NCT03614195 Completed - Stroke Clinical Trials

Effects of Three Types of Dual-task Interventions on Dual-task Walking Performance of Stroke Patients

Start date: October 24, 2018
Phase: N/A
Study type: Interventional

The objective of this study is to investigate psychometric properties of dual-task walking assessments and compare effects of three types of dual-task balance interventions on dual-task walking for stroke patients.

NCT ID: NCT03612141 Recruiting - Stroke Clinical Trials

Extern Validation of a Predictive Score of Brain Death in Severe Stroke (DIAPASON1)

DIAPASON1
Start date: February 5, 2019
Phase:
Study type: Observational

There is currently a shortage of organ in France, for patients with chronic diseases who are on the waiting list for an organ. The first source of organ donor in France is patients with brain death. 58% of patients in brain death are patients with a severe stroke ( ischemic or hemorrhagic). In order to identify which patient with a severe stroke and with unfavorable prognosis who can evolve to brain death, we have conducted a retrospective study in Lorrain, in France, and we have built a predictive score of brain death in these patients. It is important to validate this predictive score in a prospective study on a greater scale than the first study.