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Enhancement of Use-Dependent Plasticity by Somatosensory Stimulation in Chronic Stroke Clinical Trials References presented on Clinical Trials Search isn't meant to be a substitute for proven healthcare advice, trips or professional assistance using a genuine physician. We are not docs. Always confer with your physician about Enhancement of Use-Dependent Plasticity by Somatosensory Stimulation in Chronic Stroke conditions. Clinical Trials Search.org is a site devoted to listing clinical research studies in human subjects. Enhancement of Use-Dependent Plasticity by Somatosensory Stimulation in Chronic Stroke Clinical research trials and Enhancement of Use-Dependent Plasticity by Somatosensory Stimulation in Chronic Stroke healthcare trials happen in hundreds of localities throughout the United States of America. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials usually evaluate the potency of new drugs. The propose of the studies / projects is to answer particular human health questions. Clinical trials are a popular way for mDs, government agencies, and private sector companies to detect cures for all sorts of conditions, such as Enhancement of Use-Dependent Plasticity by Somatosensory Stimulation in Chronic Stroke. Enhancement of Use-Dependent Plasticity by Somatosensory Stimulation in Chronic Stroke Clinical Trials and other clinical trials allow volunteers to acquire healthcare treatment choices before they are available to the general public. Some times the subjects recieve professional assistance for free, and every now and again they are compensated for their time. Sometimes there is a cost for a Enhancement of Use-Dependent Plasticity by Somatosensory Stimulation in Chronic Stroke clinical trial. Subjects frequently obtain the most expert healthcare possible for their Enhancement of Use-Dependent Plasticity by Somatosensory Stimulation in Chronic Stroke condition. Risks are a reality, nevertheless, and can include more or frequent doctor trips, medical risks (possibly life-threatening), and/or the treatment being uneffective. Trials are federally governed with stern guidelines to protect clinical trials patients.
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Home > "E" Clinical Trials Conditions > Enhancement of Use-Dependent Plasticity by Somatosensory Stimulation in Chronic Stroke Enhancement of Use-Dependent Plasticity by Somatosensory Stimulation in Chronic Stroke
Enhancement of Use-Dependent Plasticity by Somatosensory Stimulation in Chronic Stroke
For Condition: Cerebrovascular Accident
Status: Recruiting
Sponsor(s): National Institute of Neurological Disorders and Stroke (NINDS) ,
Synopsis: Recent studies have demonstrated that electrical stimulation delivered over the skin increases the muscle strength as measured by a dynamometer in chronic stroke patients. We recently also found out that such stimulation enhances the ability of healthy brains to learn faster, enhancing the beneficial effects of the motor training. The purpose of this study is to find out if this stimulation can enhance the ability of stroke patients to experience plastic changes in the brain. It may aid in the development of new strategies for rehabilitation after brain injury in the future. A clinical and neurological exam will be administered. Each patient will participate in three different sessions separated by at least 48 hours: a 2-hour peripheral nerve stimulation to the weak hand, a 2-hour peripheral nerve stimulation to the leg, and no stimulation. The sessions will be randomly ordered. A magnetic resonance imaging scan of the brain will be done as well. Nerve stimulation will be done by transcranial magnetic stimulation (TMS). In TMS, the head is immobilized within a frame. An insulated coil wire is placed on the scalp and brief electrical current passed through it. Participants may be asked to perform movements, do simple tasks, or simply tense muscles. Electrical activity of the muscles will be recorded with a computer. Some experiments may be recorded on videotape. Participants must be stroke patients who have recovered to the point of being able to make thumb movements, and the stroke must have occurred more than 6 months ago.
Details: There are very few therapeutic options for the treatment of motor disabilities resulting from chronic stroke. Motor training results in use-dependent plasticity, thought to underlie recovery of motor function after cortical lesions. We recently demonstrated that stimulation of peripheral nerves (SPN) administered in association with motor training enhances use-dependent plasticity in healthy volunteers. The purpose of this protocol is to investigate if SPN administered in association with motor training enhances use-dependent plasticity in patients with chronic stroke. If so, it may become an important tool to enhance the beneficial effects of rehabilitative treatment in this patient group.
Eligibility:
Study Type: Interventional, Training
Minimum Age/Maximum Age: /
Genders: Both
Protocol Entry Criteria: INCLUSION CRITERIA: Hemiparetic patients (right or left who had thromboembolic non-hemorrhagic infarction (documented by CT or MRI) more than 6 months before. Patients should have recovered motor function to the point of being able to perform thumb movements. Patients will be recruited from referrals from the community, particularly Baltimore and Washington VA hospitals, and Suburban Hospital as well as stroke clubs. An anatomical MRI scan will be acquired at the NIH if a recent one (within 6 months) is not available. EXCLUSION CRITERIA: - Large hemorrhagic or brain stem stroke. - Multiple cerebral lesions with residual deficits. - History of head injury with loss of consciousness. - History of severe alcohol or drug abuse. - History of psychiatric illness. - Unstable cardiac dysrhythmia or unresponsive arterial hypertension (greater than 160/100 mmHg). - H/o hyperthyroidism. - Receiving alpha-adrenergic antagonists or agonists, major/minor tranquilizers, clonidine,prazosin, phenytoin, benzodiazepines, scopolamine, haloperidol, other neuroleptics, barbiturates. - Degree of aphasia or cognitive deficit that makes patient unable to give informed consent. - Pregnancy, glaucoma, h/o hypersensitivity or idiosyncrasy to sympatomimetic drugs.
Total Enrollment: 52
Location and Contact Information:
National Institute of Neurological Disorders and Stroke (NINDS) *Recruiting*
Bethesda, Maryland, 20892
United States
Recruiting Shashi Ravindran 3014021916
Additional Information:
Study ID Numbers: 020082; 02-N-0082
Study Start Date: December 19, 2001
Record last reviewed: December 22, 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00028379
Other Cerebrovascular Accident Studies:
1. Observational Aspirin Use and CVD in the Physicians' Health Study
2. Study of Abnormal Blood Clotting in Children with Stroke
3. Enhancement of Use-Dependent Plasticity by Somatosensory Stimulation in Chronic Stroke
4. Evaluating the Remote Effects of Stroke with MRI and PET Scans
5. Prevention of Cerebral Infarction in Sickle Cell Anemia - Comprehensive Sickle Cell Center
Related Studies:
Other Cerebrovascular Accident Clinical Trials
Other Maryland Clinical Trials
Other Bethesda Clinical Trials
Enhancement of Use-Dependent Plasticity by Somatosensory Stimulation in Chronic Stroke
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