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Stroke clinical trials

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NCT ID: NCT02076776 Completed - Stroke Clinical Trials

Heart-Brain Retraining for Stroke Rehabilitation

Start date: August 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to gain a better understanding of how different types of exercise can help people after a stroke. The investigators want to study if different types of exercise will improve the use of arm and hand function after a stroke.

NCT ID: NCT02076581 Completed - Stroke Clinical Trials

MyoSense- Automated Muscle Hypertonicity Classification System

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

It is often difficult to quantify and distinguish aspects of abnormal muscle tone due to neurological injury. This makes it difficult to evaluate therapies that aim to reduce the effects of abnormal muscle tone. This research study will evaluate the feasibility of a clinician worn device to capture and quantify features of spasticity and dystonia.

NCT ID: NCT02074111 Recruiting - Moyamoya Disease Clinical Trials

Moyamoya Disease Biomarkers in Patients With Intracranial Atherosclerotic Stroke

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

The aim of this study is to investigate the proportion of patients with moyamoya disease among the patients who were diagnosed as having intracranial atherosclerotic stroke. To do this, biomarkers (gene and imaging) for moyamoya disease are tested and follow up angiography are performed during follow up (in selected patients).

NCT ID: NCT02073955 Completed - Stroke Clinical Trials

Validation of a Community Worker Administered Stroke Symptom Questionnaire

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

This is a validation study. A stroke symptom questionnaire will be adapted and translated into local language. Two community health workers will be trained in its administration. Their findings will be validated against assessment by two neurologists. The study hypothesis is that the chance corrected agreement between the community worker administered stroke symptom questionnaire and the assessment by neurologist based on history and physical examination is at least moderate.

NCT ID: NCT02073773 Completed - Ischaemic Stroke Clinical Trials

Combinational Rehabilitative Therapy and Functional Brain Imaging for Patients Recovering From Motor Stroke

Start date: January 2014
Phase: Phase 3
Study type: Interventional

The present proposal aims to assess whether a combined rehabilitation approach using virtual reality based therapy with motivational feedback, levodopa for pharmacotherapy and standard rehabilitative occupational therapy and physiotherapy will lead to signifcantly better outcomes for stroke recovery. It is a randomised controlled trial with blinding of the assessors only. It will be preceeded by a Phase 1 pilot trial of the VR physiotherapy and standard therapy only. Recruited in-patient rehabilitation ward patients who have recently suffered stroke will be randomized, through a computer-based random number generator, to either one of two treatment arms: 1. Control occupational therapy + pharmacotherapy for 2 weeks 2. Assisted Virtual-Reality physiotherapy + pharmacotherapy for 2 weeks

NCT ID: NCT02072681 Completed - Ischemic Stroke Clinical Trials

Mild and Rapidly Improving Stroke Study

MaRISS
Start date: March 2015
Phase:
Study type: Observational [Patient Registry]

The objective of this study is to determine the 90-day outcomes of mild and rapidly improving ischemic stroke.

NCT ID: NCT02072369 Completed - Stroke Clinical Trials

Simulated Home Therapy Program for the Hand After Stroke

Start date: May 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the benefits of incorporating an actuated, EMG-controlled glove into occupational therapy of the hand.

NCT ID: NCT02072226 Terminated - Stroke Clinical Trials

A Study of the Efficacy and Safety of Alteplase in Participants With Mild Stroke

PRISMS
Start date: May 31, 2014
Phase: Phase 3
Study type: Interventional

PRISMS is a double-blind, multicenter, randomized, Phase IIIb study to evaluate the efficacy and safety of intravenous (IV) alteplase in participants with mild acute ischemic strokes that do not appear to be clearly disabling. Participants will be randomized in a 1:1 ratio to receive within 3 hours of last known well time either 1) one dose of IV alteplase and one dose of oral aspirin placebo or 2) one dose of IV alteplase placebo and one dose of oral aspirin 325 milligrams (mg).

NCT ID: NCT02069691 Completed - Stroke Clinical Trials

The Cycling Exercise With Virtual Reality Visual Stimulation for Rehabilitation in CVA Patients

Start date: August 2012
Phase: N/A
Study type: Interventional

Background: Hemiplegia is one of the main reasons why stroke survivors lose their walking and balancing ability. Many studies point out that cycling is an effective means for lower limb rehabilitation. However, during training, the unaffected limb may compensate for the affected one resulting in suboptimal rehabilitation. To address this issue, the investigators developed the virtual reality-cycling training system (VRCTS) which can acquire force and speed signals in real-time through a cycling module. The system then analyzes the acquired data and uses a 3D VR rehabilitation program to help patients to train their affected side. The aim of the study was to develop the VRCTS, verify its function and test system function on both normal subjects and stroke patients. Methods: In this system, the investigators designed a cycling device that is embedded with load cell and encoder sensors to detect cycling force and angle in real-time. A Cycling Graph User Interface Control and Data Recode System (Cycling CR System) was applied for signal analysis and feedback control. The investigators designed a 3D interactive VR rehabilitation program that can guide and train the users through visual feedback. Each user performed a pre-test to examine determine condition, left-right balance and other parameters, which allows the system to be customized.

NCT ID: NCT02068664 Completed - Stroke Clinical Trials

An Assessment of the Prevalence of Spatial Neglect in Stroke Survivors With Aphasia

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

The purpose of this study is to determine if stroke survivors with aphasia have spatial neglect (Phase 1). If they are determined to have the condition Phase 2 will be offered: which is prism adaptation treatment. This is a pilot study that will be performed with 4-5 subjects.