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Stroke clinical trials

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NCT ID: NCT02917850 Withdrawn - Stroke Clinical Trials

Impact of Hip Flexors Isokinetic Strengthening on Gait Capacities in Subacute Stroke Patients

ISOKINETIC
Start date: August 2016
Phase: N/A
Study type: Interventional

Post-stroke patients often present with gait disorders due to several physical impairments. Hip flexor deficit is one of the more prevalent trouble and is associated with gait capacities. This study aims at evaluating the impact of an isokinetic hip flexors strengthening rehabilitation program in the subacute phase after stroke. Patients will be randomized to an intervention group (isokinetic rehabilitation) or a control group (conventional rehabilitation) and assessed at the end of the rehabilitation program, at 3 and at 6 months.

NCT ID: NCT02917343 Completed - Stroke Clinical Trials

Effect of Mirror Therapy and Task Oriented Training for Persons With Paretic Upper Extremity

Start date: October 2014
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the effect of a combined mirror therapy and task oriented/repetitive task training on upper extremity function of persons with hemiplegia due to cerebrovascular accident or stroke.

NCT ID: NCT02917213 Completed - Stroke Clinical Trials

Imaging Silent Brain Infarct And Thrombosis in Acute Myocardial Infarction

ISBITAMI
Start date: September 2016
Phase:
Study type: Observational

This project aims to assess the ability of cardiac imaging (cardiac MRI and Doppler-echocardiography) post-processing tools to predict a combined end-point of intraventricular thrombosis, silent brain infarcts, clinical stroke and peripheral arterial embolism in patients with first acute myocardial infarction and ventricular dysfunction.

NCT ID: NCT02916797 Completed - Clinical trials for Cerebrovascular Accident

Stepping Training Using Feedback in Stroke

Start date: April 10, 2016
Phase: N/A
Study type: Interventional

- Are there differences in immediate effects of stepping training with and without the use of visually weight-taking machine (VWTM) on variables relating to well-controlled walking and walking symmetry in ambulatory patients with stroke? - Are there differences of 4-week stepping training with and without the use of VWTM on variables relating to well-controlled walking and walking symmetry in ambulatory patients with stroke?

NCT ID: NCT02916030 Completed - Stroke Clinical Trials

Vitamin D and Stroke

Start date: September 1, 2016
Phase:
Study type: Observational

Stroke remains one of the most devastating neurological diseases, often causing death, or gross physical impairment. It is the second most common cause of death worldwide and a major cause of acquired disability in adults.Vitamin D deficiency has been reported to contribute to the risk of cardiovascular disease especially stroke.

NCT ID: NCT02915484 Terminated - Stroke Clinical Trials

Transcranial Direct Current Stimulation (tDCS) in Chronic Post-Stroke Apathy

TDCS-PSA
Start date: June 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to test the efficacy and safety of tDCS (Transcranial Direct Current Stimulation) on apathy in stroke patients.

NCT ID: NCT02915185 Completed - Stroke Clinical Trials

Brain Stimulation and Tailored Interventions to Promote Recovery in Stroke Survivors

Start date: April 28, 2017
Phase: N/A
Study type: Interventional

A substantial proportion of individuals are left with poor residual functioning of the affected arm after a stroke. This has a tremendous impact on the quality of life and the ability for stroke survivors to live independently. While exercise is considered essential to any rehabilitation program, its benefits are generally far from optimal because of the lack of proper dosing in terms of intensity. One way to tackle this problem is to develop better tools that could predict an individual's potential and then adjust the intensity of exercise accordingly. One such predicting tool exists and consists of using non-invasive brain stimulation such as transcranial magnetic stimulation (TMS), to assess the integrity of descending motor pathways originating from the brain. TMS consists of applying a magnetic wand near the scalp to stimulate brain cells without inducing pain or discomfort. One goal of the current proposal is to use TMS to test the integrity of the motor pathway in chronic stroke survivors. The level of responses to TMS will be used to classify participants in terms of potential for recovery and then, to determine the optimal level of exercise. The study will also examine the effect of another non-invasive brain stimulation technique called transcranial Direct-Current Stimulation-tDCS to determine whether it can enhance the response to strength training exercise in the affected arm. Half of the participants will be trained with the tDCS on, while the other half will be trained with the stimulator off. The training program will last 4 weeks; 3X/week. Both clinical and neurophysiological measures will be performed to determine the impact of the strength training intervention on participants. Overall, the proposed project is expected to have a positive and significant impact on stroke survivors' quality of life.

NCT ID: NCT02914106 Completed - Ischemic Stroke Clinical Trials

Neuroactive Steroids in Acute Ischemic Stroke

Start date: June 2014
Phase: N/A
Study type: Observational

Despite several scientific and technological advances, there is no single neuroprotective treatment that can reverse the brain damage after acute ischemic stroke (AIS). Neuroactive steroids are cholesterol-derived hormones that have the ability to modulate the normal and pathologic nervous system employing genomic and non genomic mechanisms. In this work, we first investigated if AIS affects the plasma concentration of five neuroactive steroids (cortisol, estradiol, progesterone, testosterone and 3-alpha androstenediol glucuronide). Second, we studied if levels of circulating steroids associate with neurological, cognitive and functional outcome in a cohort of 60 to 90 year-old male and female patients with AIS. For this purpose, we recruited patients who were hospitalized at the Emergency Room of the Central Military Hospital within the first 24 hours after stroke onset. We designed two experimental groups, each one composed of 30 control subjects and 30 AIS patients, both males and females. The assessment of neurological deficit was performed with the NIHSS and the tests used for the functional and cognitive status were: (1) modified Rankin Scale; (2) Photo test and (3) abbreviated Pfeiffer's mental status questionnaire.

NCT ID: NCT02913183 Not yet recruiting - Stroke Clinical Trials

Efficacy and Safety of Young Health Plasma on Acute Stroke

Start date: October 2016
Phase: Phase 2
Study type: Interventional

Stroke is one of the main severe disease of public health importance. Recent studies showed that old age is one of the most important factors in influencing the outcome of patients with acute stroke, and the young plasma can reverse age-related brain impairments in mice. Therefore, this pilot study aims to investigate whether young plasma is effective in alleviating brain injury and neurologic deficits induced by acute stroke in patients.

NCT ID: NCT02912923 Completed - Stroke Clinical Trials

Reaching in Stroke 3rd Phase

RISP3
Start date: September 14, 2016
Phase: N/A
Study type: Interventional

The project targets stroke survivors to investigate the effect of augmented feedback (using robotic force cues and visual feedback) and rewards (game scores), on their upper limb reaching patterns and trunk compensatory movements