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Active clinical trials for "Paresis"

Results 241-250 of 409

Relationship Between Nutritional State and Respiratory Muscle Weakness in Adult Patients With Bronchietasis...

Bronchiectasis

To establish a relationship between malnutrion and respiratory muscle dysfunction in patients with bronchectasis

Active2 enrollment criteria

The Effects of Mirror-Based Virtual Reality Systems and Recalibration Software on Upper Extremity...

StrokeHemiparesis

The goal of this study is to learn about the benefits of using a virtual reality gaming system that can be adjusted for a person who has upper arm weakness from stroke. The main question it aims to answer is whether strength and movement in the upper arm be improved by use of the gaming system. Participants will be asked to complete initial measurements of upper arm function, play a video game for one hour, four times a week for five weeks, and repeat the measurements of upper arm function at the end.

Completed9 enrollment criteria

Post-parotidectomy Facial Paresis: Intraoperative and Postoperative Factors

Parotid NeoplasmsFacial Paralysis

This is a protocol to govern the prospective trial of facial nerve monitoring in patients undergoing parotidectomy with an eye towards interpreting if the facial nerve monitor provides useful information to operating surgeons and if the information provided by the facial nerve monitor can predict degrees of postoperative facial nerve paresis. Additionally, the study will determine if performing daily facial rehabilitation exercises provides a benefit in reducing time to recovery of temporary post-parotidectomy paresis.

Completed11 enrollment criteria

A Study in Older Participants Who Have Fallen and Have Muscle Weakness

Muscle Weakness

LY2495655 is an investigational drug being tested for muscle wasting.

Completed28 enrollment criteria

Stroke Wearable Operative Rehabilitation Device Impact Trial

Ischemic StrokeUpper Extremity Hemiparesis

The objective of this study is to determine the impact of vibratory feedback on the quality and intensity of a common motor rehabilitation task of the upper-arm (hand-to-mouth) in stroke patients. For that purpose the investigators use the SWORD system that combines 3D motion quantification wearable sensors and a vibratory module. The investigators hypothesize that vibratory stimuli during a motor rehabilitation task increase significantly the number of correct movements performed per unit of time. The design of the study is a cross-over randomized clinical trial. With the SWORD system in place each patient will perform the hand-to-mouth task twice (with vibratory feedback and without it), the order being random. The number of correct movements and other motor outcomes will be assessed continuously under both conditions.

Completed19 enrollment criteria

Muscle Weakness Duration After Single Botulinum Toxin Injection in Masseter

Bite ForceBotulinum Toxins1 more

This study aimed to evaluate the duration of a reduced maximal voluntary bite force after a botulinum toxin intervention. Methods: In an intervention group, 25 units of Xeomin® (Merz Pharma GmbH & Co KGaA, Frankfurt am Main, Germany) botulinum neurotoxin type A were injected into the masseter muscles bilaterally (to a total of 50 units).

Completed2 enrollment criteria

Early Independent Adaptive Arm and Hand Rehab

Post-stroke Hemiparesis

The purpose of this study is to test the hypothesis that early independent adaptive bimanual-to-unimanual training of arm and hand movements, assisted with specially designed mechanical devices: the mirrored motion bimanual arm trainer (m2 BAT), will improve motor control and function in patients with post-stroke hemiparesis.

Completed13 enrollment criteria

Vibrational-proprioceptive Resistance Exercise Training Versus Neuromuscular Electrical Stimulation...

Muscle Weakness ConditionTherapy Effect

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

Completed18 enrollment criteria

Motor Task Performance Under Visual and Auditory Feedback Post Stroke: a Randomized Crossover Trial...

Ischemic StrokeUpper Extremity Paresis

The study was designed to evaluate the impact of a novel kinematic biofeedback system - SWORD - in the motor performance of patients after stroke. The SWORD system combines inertial motion trackers and a mobile app, allowing digitization of patient motion and providing real-time audiovisual biofeedback. The investigators hypothesize that the biofeedback feedback provided by the SWORD system improves patient performance, defined as an increase in the number of correct movements. The design of the study is a cross-over randomized clinical trial. Patients will be randomized into two groups. Both will perform two separate sessions consisting of one exercise - shoulder flexion with elbow flexion at 90 degrees - for 4 minutes in both experimental settings: with and without biofeedback. Group 1 will perform the exercise with biofeedback first and without biofeedback after, with an interval >24h. Group 2 will perform the exercise in the opposite order. The SWORD system will be used to record movement data in both sessions, but the feedback was only active in one of them.

Completed10 enrollment criteria

Mental Imagery Neurofeedback in Strokerehabilitation

StrokeHemiparesis

This research project will investigate neurofeedback training in stroke rehabilitation during which patients receive feedback in real time from their brain activity measured with ElectroEncephaloGraphy (EEG). The investigators hypothesize that the feedback training allows to internally stimulate brain motor networks in order to promote functional recovery of the hand.

Completed12 enrollment criteria
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