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Stroke clinical trials

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NCT ID: NCT03062319 Recruiting - Atrial Fibrillation Clinical Trials

Optimal Antithrombotic Therapy in Ischemic Stroke Patients With Non-Valvular Atrial Fibrillation and Atherothrombosis

ATIS-NVAF
Start date: April 6, 2017
Phase: Phase 4
Study type: Interventional

The Purpose of this open-label randomized controlled multicenter trial is to evaluate the efficacy and safety of mono-drug therapy with oral anticoagulant compared to combination therapy with antiplatelet drug, in ischemic stroke patients with non-valvular atrial fibrillation and atherothrombosis.

NCT ID: NCT03059225 Recruiting - Stroke Clinical Trials

rTMS in Aphasic Patients With Neuroimage Assessments

Start date: February 18, 2017
Phase: N/A
Study type: Interventional

The refinement of repetitive transcranial magnetic stimulation (rTMS) has highlighted its merit in terms of learning programs as a treatment for aftereffect augmentation. Nevertheless, the efficacy of synchronous rTMS protocol integrated with computer-integrated speech training is not well understood. It is also not clear regarding the efficacy of compound bi-hemispheric stimulation protocol. The aim of the study is to investigate language response to these new strategies and to determine the longevity of the therapeutic outcome. Advanced MR neuroimaging techniques, such as fMRI and DTI, are powerful tools to evaluate the concomitant nervous changes after rTMS treatment on aphasic patients. The knowledge from fMRI and DTI microstructural evolution provides insight into underlined mechanism operating the language improvement.

NCT ID: NCT03058796 Completed - Stroke Clinical Trials

Contralaterally Controlled Functional Electrical Stimulation Plus Video Games for Hand Therapy After Stroke

Start date: June 19, 2017
Phase: Phase 2
Study type: Interventional

Determine if adding a video game component to an electrical stimulation therapy improves hand function in stroke patients

NCT ID: NCT03058770 Completed - Stroke Clinical Trials

Sensorimotor Retraining in Chronic Stroke

Start date: February 16, 2017
Phase: N/A
Study type: Interventional

A prospective, randomized double-blind clinical trial will be conducted to determine the effect of a sensorimotor retraining program on the sensory and functional recovery of the paretic lower limb of subjects with chronic sequelae from stroke.

NCT ID: NCT03056287 Completed - Stroke Clinical Trials

Exercise and Brain Stimulation for Post-stroke Depression

Start date: January 1, 2016
Phase: N/A
Study type: Interventional

This project will assess the effects of aerobic exercise training (AET), repetitive transcranial magnetic stimulation (rTMS) or their combination on depressive severity as well as locomotor function in persons with post-stroke depression (PSD). Both AET and rTMS are established stand-alone treatments for non-stroke related depression, though neither has been adequately studied post-stroke. Furthermore, substantive research indicates that AET improves post-stroke locomotor function, thus offering a novel approach for treating PSD as well as an established vehicle to study the effects of PSD on response to rehabilitation. The purpose of this project is to determine the impact of AET, rTMS and their combination (AET+rTMS) treatments on post-stroke depressive symptoms and locomotor function so as to guide the development of a future clinical trial. A total of 40 depressed post-stroke subjects will be randomly assigned to one of four groups 1) AET; 2) rTMS; 3) combined AET and rTMS (AET+rTMS) or 4) control (sham rTMS) group (n=10 per condition; equally distributed with mild and moderate MDD). Further, an additional 10 non-depressed post-stroke subjects will complete 8 weeks of AET so as to allow us to determine the effects of PSD on response to training (Aim 2). Training (AET, rTMS and AET+rTMS) will take place over an 8-week period, three times per week on non-consecutive days. Measures of depression (HRSD17) as well as self-selected walking speed (SSWS) will be performed prior to the initial treatment session of each week as well as 8 weeks following cessation of treatment. Additional measures of locomotor function (walking endurance and amount of daily community stepping) will be assessed prior to training (pre), following 4 weeks of training (mid), upon completion of 8 weeks of training (post) as well as 8 weeks following cessation of training (follow-up), allowing determination of the efficacy (and persistence) of training on these outcomes.

NCT ID: NCT03054974 Recruiting - Stroke Clinical Trials

TCM Clinical Practice Rehabilitation of Post-stroke Spasticity

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

The purpose of this study is to determine the effectiveness,safety and Input-output ratio of chinese traditional treatment in spasm after stroke,both in massage and herbal medicine bathing.

NCT ID: NCT03054064 Completed - Stroke Clinical Trials

Evaluating the Indego Exoskeleton for Persons With Hemiplegia Due to CVA

Start date: February 21, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of the Indego exoskeleton as a gait training tool for individuals with hemiplegia due to Cerebrovascular Accident (CVA).

NCT ID: NCT03053492 Completed - Stroke Clinical Trials

Functional Viability Duck Duck Punch

DDPSBIR
Start date: January 10, 2017
Phase: N/A
Study type: Interventional

This study has 2 parts: In one part of this study, people with stroke will either play a custom designed computer game for stroke rehabilitation called Duck Duck Punch or an off the shelf computer game with their weaker arm 3 times per week for 6 weeks. Evaluations will determine whether or not one computer game improved arm movement more than the other. In the second part of the study, people with stroke, caregivers of people with stroke and stroke rehabilitation therapists will meet in several focus groups to design a useful and informative Duck Duck Punch performance report.

NCT ID: NCT03053154 Completed - Stroke Clinical Trials

Relationship Between Pelvic Tilt and Sit to Stand Task in Stroke Patients

Start date: September 2016
Phase: N/A
Study type: Observational

The purpose of this study is to assess and determine the influence of pelvic inclination on sit to stand task in stroke patients.

NCT ID: NCT03052712 Terminated - Stroke Clinical Trials

Validation and Standardization of a Battery Evaluation of the Socio-emotional Functions in Various Neurological Pathologies

GREFEXII
Start date: September 9, 2016
Phase: N/A
Study type: Interventional

The role of disorders of socio-emotional processes in cerebral diseases such as Alzheimer's disease, frontal temporal dementia, Parkinson's disease, Huntington's disease, traumatic brain injury, stroke, focal lesions, has been recognized recently. Social cognition refers to a large group of emotional and cognitive abilities regulating inter-individuals relationships and it includes mainly theory of mind, emotional information processing and empathy. However, assessment of socio-emotional processes is still largely based on experimental tests that are not validated for clinical purpose. In addition their long duration of administration is not adapted to clinical examination. Finally these tests have not been standardized and normalized in French-speaking population.