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Paresis clinical trials

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NCT ID: NCT01704976 Completed - Muscle Weakness Clinical Trials

SR-WBV Training for Frail Elderly in the Skilling up Stage

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

This randomized controlled study aims to examine long term effects in the skilling up phase over 4 weeks on physical functional performance and strength of mechanical SR-WBV and dance therapy intervention in a frail elderly population.

NCT ID: NCT01688856 Completed - Stroke Clinical Trials

Contralaterally Controlled FES of Arm & Hand for Subacute Stroke Rehabilitation

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

Impaired arm and hand function is one of the most disabling and most common consequences of stroke. The Investigators have developed Contralaterally Controlled Functional Electrical Stimulation (CCFES), an innovative neuromuscular electrical stimulation (NMES) treatment for improving the recovery of hand function after stroke. The purpose of this study is to maximize the treatment effect of CCFES by adding stimulated elbow extension. The specific aims and hypotheses are as follows: AIM 1: Estimate the effect of Arm+Hand CCFES on upper limb motor impairment and activity limitation. Hypothesis 1: Stroke survivors treated with Arm+Hand CCFES have better outcomes on upper limb impairment and activity limitation measures than those treated with dose-matched Arm+Hand Cyclic NMES. AIM 2: Estimate the effect of adding stimulated elbow extension to Hand CCFES. Hypothesis 2: Stroke survivors treated with Arm+Hand CCFES will have greater reductions in upper limb impairment and activity limitation than those treated with Hand CCFES. AIM 3: Describe the relationship between treatment effect and time elapsed between stroke onset and start of treatment. Hypothesis 3: Patients who start Arm+Hand CCFES sooner after their stroke achieve better outcomes.

NCT ID: NCT01679977 Completed - Clinical trials for Muscle Weakness Condition

Vibrational-proprioceptive Resistance Exercise Training Versus Neuromuscular Electrical Stimulation Training in Elderly People With Muscle Weakness

MOBIL
Start date: June 2008
Phase: N/A
Study type: Interventional

Study the structural behaviours of weak muscle of elderly and evaluate the efficiency of two different types of training.

NCT ID: NCT01662960 Completed - Stroke Clinical Trials

Visual Feedback Therapy for Treating Individuals With Hemiparesis Following Stroke

Start date: September 7, 2012
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether an existing treatment for problems that participants have with making movements after a stroke can be performed at home.

NCT ID: NCT01658293 Completed - Stroke Clinical Trials

Thermal Stimulation for Stroke Patients

TSSP
Start date: August 1, 2012
Phase: N/A
Study type: Interventional

Sensory and/or motor deficits in upper limb following stroke often have negative impacts on their daily living. Thermal stimulation with hot and cold pack alternatively incorporated into conventional rehabilitation has been reported and proved to be effective for upper limb functional recovery after stroke. However, whether hot- and cold-water stimulation alternatively based on thermal stimulation also has the effect still remains unknown. The aim of present study is to investigate the facilitated effect of hot and cold water stimulation alternatively on upper limb after stroke.

NCT ID: NCT01655277 Completed - Fall Risk Clinical Trials

Ultrasound Guided Adductor Canal Block Versus Femoral Nerve Block for Quadriceps Strength and Fall-risk

Start date: February 2012
Phase: Phase 4
Study type: Interventional

Our objective was to determine if an ultrasound guided ACB can preserve quadriceps strength, thus minimizing weakness of knee extension compared with ultrasound guided femoral nerve block. Our primary outcome was the percent of maximum voluntary isometric contraction (MVIC) of knee extension preserved at 30 mins after either an ACB or FNB. Secondary outcomes included MVIC of knee extension at 60 min, hip adduction at 30 and 60 mins, and assessment of fall risk with the Berg Balance Scale (BBS) at 30 minutes.

NCT ID: NCT01654315 Completed - Hemiparesis Clinical Trials

Robotic Brace Incorporating Electromyography for Moderate Affected Arm Impairment After Stroke

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

Of the 5.7 million stroke survivors in the United States, up to 80% exhibit significant weakness in one arm (called "hemiparesis"). This devastating impairment undermines performance of valued activities and quality of life. Although rehabilitation is commonly provided, conventional affected arm rehabilitative strategies have negative evidence, or no evidence, supporting their use. Thus, there remains a need for evidence-based rehabilitative strategies for arm hemiparesis. Newer rehabilitative approaches emphasize repetitive, task-specific practice (RTP) incorporating the affected arm. However, many of these promising regimens require participation in intensive therapies, and most are only efficacious on the least impaired patients. Thus, there remains a need for an efficacious, practical RTP technique to address moderate affected arm hemiparesis. To address the above shortfalls, one of the investigators team members piloted an innovative brace integrating electromyography (EMG) and robotics. In his case series, 8 stroke patients exhibiting moderate arm impairment successfully participated in RTP, with the brace (called the "Myomo") detecting and augmenting their movement attempts. Aided by the Myomo, participation in the RTP regimen reduced subjects' affected arm impairment and spasticity. The next logical step is to test Myomo + RTP efficacy using randomized controlled methods and an appropriate sample size.

NCT ID: NCT01651533 Completed - Hemiparesis Clinical Trials

Mental Practice in Chronic, Stroke Induced Hemiparesis

Start date: September 2010
Phase: N/A
Study type: Interventional

Stroke is the leading cause of disability in the United States, producing motor impairments that compromise performance of valued activities. Hemiparesis (or weakness in one arm) is particularly disabling, is the primary impairment underlying stroke-related disability, and the most frequent impairment treated by therapists in the United States. This study will test efficacy of a promising technique in reducing arm disability and increasing function, thereby improving outcomes and health, reducing care costs, for community dwelling patients with stroke-induced hemiparesis.

NCT ID: NCT01646216 Completed - Stroke Clinical Trials

Long Term Split Belt Treadmill Training for Stroke Recovery

Start date: June 7, 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether split belt or conventional treadmill training can be used to treat walking pattern deficits from stroke and to determine whether this improves gait asymmetry and metabolic efficiency.

NCT ID: NCT01640041 Completed - Hemiparesis Clinical Trials

Feasibility Study for Enhancing Gait Following Stroke With Implanted Microstimulators

Start date: May 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to test an innovative, advanced FNS microstimulator technology developed by the Alfred Mann Foundation (Santa Clarita, CA) called, the Radio Frequency Microstimulation (RFM) Gait System that promises to provide FNS training for restoration of functional gait components in a manner at least as efficacious as current investigational FNS systems. The design features of the RFM Gait System are intended to address the problems with the current FNS systems. The RFM implant devices are small enough to be inserted using only a 5 mm incision[3]. Because both the electrode (anode and cathode) are contained within the microstimulator, there are no lead wires traversing the skin, joints, or torso/limb junctures. Individual RFMs can be inserted at the motor points and nerves of each of the paretic muscles in the involved limb and coordinated using radio frequency technology.