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Stroke clinical trials

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NCT ID: NCT02734082 Completed - Stroke Clinical Trials

The Brain Heart Interaction in Acute Stroke

Start date: October 2013
Phase: N/A
Study type: Observational

Many studies have shown that acute cerebral dysfunction can impair cardiac function and autonomic control of blood pressure, heart rate and vascular tone, however, the size of the stroke is rarely reported. Involvement of the insular cortex seems to predispose to cardiac damage and autonomic dysfunction. However, it is not clear whether cardiac dysfunction is merely a marker of large strokes or location of the stroke is critical.

NCT ID: NCT02731508 Recruiting - Stroke Clinical Trials

Repetitive Bihemispheric Transcranial Direct Current Stimulation After Stroke

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

Non-invasive repetitive bi-hemispheric transcranial direct current stimulation (tDCS) may restore post-stroke bi-hemispheric balance by increase peri-lesional cortex activity and suppress abnormal inhibition from non-lesional hemisphere, and therefore enhance after-effects of rehabilitation. In this double-blind, randomized controlled trial, investigators aim to investigate whether multi-session, bihemispheric tDCS to the primary motor cortex (M1) in combination with upper extremity rehabilitation therapy affected motor functional outcome, ipsilesional motor circuit excitability using transcranial magnetic stimulation (TMS) and magnetoencephalography (MEG) measures.

NCT ID: NCT02731235 Active, not recruiting - Stroke, Lacunar Clinical Trials

The Effect of Aerobic Exercise in Patients With Lacunar Stroke

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

In a randomized-controlled study the effect of high-intensity training, 5 days a week at home for 12 weeks is tested in patients with lacunar stroke.

NCT ID: NCT02730455 Completed - Clinical trials for Acute Ischemic Stroke

Safety and Efficacy of Intravenous Natalizumab in Acute Ischemic Stroke

ACTION2
Start date: July 18, 2016
Phase: Phase 2
Study type: Interventional

The primary objective of the study is to assess the clinical effects of natalizumab versus placebo in acute ischemic stroke on clinical measures of functional independence and activities of daily living. The secondary objective of the study is to explore dose and exposure response and the clinical treatment effects of natalizumab versus placebo in acute ischemic stroke on the following: measures of independence, activities of daily living, neurologic function, quality of life, cognition, and safety and tolerability

NCT ID: NCT02728180 Active, not recruiting - Clinical trials for Acute Ischemic Stroke

Xingnaojing for Moderate-to-severe Acute Ischemic Stroke (XMAS)

XMAS
Start date: March 2016
Phase: Phase 4
Study type: Interventional

The main purpose of this trial is to determine whether Xingnaojing, intravenously administered within 24 hours of symptom onset, improves the 3-month outcome in participants with acute ischemic stroke.

NCT ID: NCT02726685 Not yet recruiting - Stroke Clinical Trials

Effects of Respiratory Training on Respiratory and Functional Performance in Patients With Stroke

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

The purpose of the research is to investigate the effects of respiratory training on respiratory and functional performance in patients with stroke.

NCT ID: NCT02726204 Completed - Stroke Clinical Trials

Evaluation of a Wearable Exoskeleton for Functional Arm Training

Start date: June 1, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate how the cable-driven arm exoskeleton (CAREX) can assist task performance during 3D arm movement tasks under various experimental conditions in healthy individuals and patients with stroke. This study is designed to test motor learning with the robotic rehabilitative device CAREX under three conditions in healthy subjects and subjects with post-stroke hemiparesis.

NCT ID: NCT02725944 Completed - Atrial Fibrillation Clinical Trials

Prediction and Detection of Occult Atrial Fibrillation in Patients After Acute Cryptogenic Stroke and TIA

PROACTIA
Start date: May 15, 2016
Phase:
Study type: Observational

PROACTIA is a prospective, event-driven observational study. It aims to propose a composite scoring system in order to evaluate the risk of paroxysmal atrial fibrillation (PAF) in patients after acute cryptogenic stroke and transient ischemic attack (TIA).

NCT ID: NCT02725853 Completed - Stroke Clinical Trials

Enhancing Recovery of Arm Movement in Stroke Patients

ENHANCE
Start date: June 2016
Phase: N/A
Study type: Interventional

Many people who have had a stroke have problems recovering the use of their affected arm and these problems may persist for a long time. The investigators' research will test new ways to boost recovery by using non-painful brain stimulation together with training of arm movements using basic science principles. The training program will be done using the latest technology in rehabilitation such as virtual reality and robotics. The investigators will compare three groups of patients who have had a stroke. Each group will receive different combinations of brain stimulation and arm training. Another aspect of this proposal is that the investigators will do the same training programs in three different countries - Canada, Israel and India. In this way, the investigators will combine knowledge and skills to create training programs that can be applied anywhere in the world and that are not necessarily limited to high-income countries. Also, by combining expertise, the investigators will help to build the capacity to do research in India, a middle-income country that has great potential to contribute new knowledge to rehabilitation medicine.

NCT ID: NCT02724813 Completed - Stroke Clinical Trials

Tele-Rehabilitation Study for People With a History of Stroke

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

Stroke results in long-term disability for many people, and particularly for survivors of stroke who have cognitive impairments. However, a decreasing proportion of stroke patients are able to access or receive publicly funded rehabilitation. The investigators have shown in previous studies that in-person delivery of the Cognitive Orientation to daily Occupational Performance (CO-OP) rehabilitation approach to promoting attainment of everyday life goals has resulted in improvements in functional independence and executive function. In a small pilot study of tele-CO-OP with people with chronic traumatic brain injury (TBI) (n=3), the investigators found the delivery method was feasible and that participants were satisfied with the treatment and demonstrated clinically significant improvements on personally meaningful activities. The investigators will investigate the feasibility, preliminary efficacy, and cost-effectiveness of delivering CO-OP in an online format to reduce disability post-stroke. The study design is a single-blind (assessor), randomized wait-list control trial with a one-month retention follow-up. All therapy and testing sessions will be delivered online. We hypothesize that participants will demonstrate improvement in everyday activities and community participation.