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Stroke clinical trials

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NCT ID: NCT02701998 Recruiting - Stroke Clinical Trials

The Stroke and Exercise Program

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

This study involves a randomized controlled trial to test the feasibility, acceptability, and efficacy of a mobile health (mHealth)-enhanced physical activity (PA) intervention to increase daily bout-related and total moderate-intensity PA and to reduce sedentary behavior (SB) in non-physically impaired patients with ischemic stroke or transient ischemic attack (TIA).

NCT ID: NCT02700945 Completed - Stroke, Acute Clinical Trials

Rate of Atrial Fibrillation Through 12 Months in Patients With Recent Ischemic Stroke of Presumed Known Origin

Start date: March 2016
Phase: N/A
Study type: Interventional

The purpose of the Stroke AF study is to compare the incidence of atrial fibrillation (AF) through 12 months between continuous cardiac rhythm monitoring with the Reveal LINQ™ Insertable Cardiac Monitor (ICM) (continuous monitoring arm) and standard of care (SoC) medical treatment (control arm) in subjects with a recent ischemic stroke of presumed known origin.

NCT ID: NCT02700061 Active, not recruiting - Stroke Clinical Trials

Effects of Upper Limb Motor and Robotic Training Over Neuroplasticity and Function Capacity

NARLE1
Start date: February 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate and compare the effects of upper limb training with Induced Constraint Therapy (ICT) or robotic therapy. No placebo therapy is used. Motor function, neurological evaluations and quality of life are assessed for the comparison of the therapies.

NCT ID: NCT02699775 Recruiting - Clinical trials for Botulinum Toxins Injection in Stroke Patients

Effect of Repeated Botulinum Toxin Injection on Gait Pattern in Stroke Patients

TRITITOX
Start date: December 12, 2017
Phase: N/A
Study type: Observational

Chronic stroke patients exhibit gait pattern alterations which are mainly due to spasticity and treated with repetitive multifocal botulinum toxin injection(BTI). Several studies demonstrated that single BTI-session in a single muscle of paretic lower limb(LL) improved kinematic gait parameters(GP) but surprisingly none of them assessed the effects of repetitive multifocal BTI on patient's gait pattern and their duration. The aim was to evaluate the impact of repetitive multifocal BTI-sessions on GP of chronic stroke patients. To that end, gait of patients will be compared using 3D-gait analysis after 3 consecutives BTI sessions.

NCT ID: NCT02699398 Completed - Stroke Clinical Trials

Domiciliary VR Rehabilitation

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

The purpose of this study is to determine whether domiciliary VR-based telerehabilitation is superior than domiciliary occupational therapy for inducing functional gains, enhancing corticospinal excitability, and cortical reorganization.

NCT ID: NCT02698605 Completed - Stroke Clinical Trials

Evaluation of the Arm Rehabilitation Device for Patients With Stroke

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

The usability assessment focuses on the actual use of the proposed rehabilitation system to clarify issues users would face in actual system operation, thus providing a reference for subsequent system improvement.

NCT ID: NCT02694302 Completed - Stroke Clinical Trials

Clinical Trial of Robot-assisted-gait-training (RAGT) in Stroke Patients

Walkbot
Start date: March 2014
Phase: N/A
Study type: Interventional

A clinical trial of robot-assisted-gait-training (RAGT) in stroke patients to evaluate its efficacy, safety over conventional gait training.

NCT ID: NCT02693834 Completed - Stroke Clinical Trials

Effects of Two Different Types of Ankle Foot Orthoses on Gait Outcomes in Patients With Subacute Stroke.

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

PURPOSE: The purpose of this study will be to identify whether patients in the subacute stage of stroke, who demonstrate foot drop, will have better gait outcomes when using a Double Adjustable AFO, or a Posterior Leaf Spring AFO. A secondary purpose will be to determine whether one week of practice significantly changes gait outcomes with either of the AFO conditions. INCLUSION CRITERIA: Twenty participants over the age of 18, of any gender and ethnicity, diagnosed with first time unilateral stroke, 4 - 20 weeks post-stroke onset, resulting in hemiparesis with foot drop will be recruited for this study. EXCLUSION CRITERIA: 1. Not able to receive a double adjustable AFO through their insurance 2. Unable to follow two steps commands 3. Unable to ambulate 20 feet with or without assistive device with a minimum level of assistance of contact guard assistance. 4. Cerebellar Stroke 5. Inability to ambulate prior to stroke 6. receiving chemotherapy at the time of study OUTCOME MEASURES: 1. Six Minute walk test 2. Gait Symmetry and Gait velocity measured with GAITRite for self paced velocity walk and fast paced velocity walk. DATA COLLECTION: Data will be collected three times over two weeks period. First Visit: Demographics, Fugl-Meyer Lower Extremity Assessment of sensorimotor function, Mini Mental State Examination 6MWT and GAITRite measurements using Both types of AFO in a random order. Afterwards participant will be given one type of AFO (randomly selected) to practice walking for a week. Second Visit: 6MWT and GAITRite measurements using the type of AFO they were practicing with. Then the other type of AFO will be given to practice walking for a week. Third Visit: 6MWT and GAITRite measurements using the second type of AFO that they were practicing with the week prior. Patient will be asked which type of AFO they prefer to use.

NCT ID: NCT02693223 Recruiting - Stroke Clinical Trials

Get With the Guidelines-Stroke Registry

GWTG-Stroke
Start date: January 2003
Phase:
Study type: Observational [Patient Registry]

Get With The Guidelines-Stroke is a program for improving the quality of care for patients hospitalized with stroke by promoting consistent adherence to the latest evidence-based clinical practice guidelines.

NCT ID: NCT02690493 Completed - Stroke Clinical Trials

The Efficacy of an Acupuncture Protocol and Use of Taping in the Treatment of Spastic Upper Limb After Stroke

Start date: January 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether acupuncture and taping are effective in the treatment of spastic upper limb after stroke.