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Gait clinical trials

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NCT ID: NCT03204747 Completed - Multiple Sclerosis Clinical Trials

Effect of Need to Void on Gait Speed in Multiple Sclerosis

Start date: February 27, 2017
Phase:
Study type: Observational

Multiple sclerosis causes demyelinating lesions, which can induce multiple symptoms. If motor disorders are the most visible disability, urinary disorders are frequent, with prevalence from 32 to 86%. The first ones are due to pyramidal, cerebellar or proprioceptive lesions. The seconds are due to specific lesion in inhibitor/activator encephalic centers, or interruption on medullary conduction. It seems to be evident that walk and urinary disorders are link, because of similar anatomic ways and control process. Effect of bladder filling is well known on motoneuronal excitability. The effect of bladder filling on walk stay unknown, while medullary integration of these two functions is very close, in medullary cone. Primary aim is to assess the effect of need to void on walk speed in multiple sclerosis with lower urinary tract symptoms. Secondary aim is to identify clinical or urodynamic factor link with major walk impairment when patients need to void. Patient with multiple sclerosis over 18 years old, consulting for lower urinary tract symptoms in a tertiary center are included. History and treatment, high, weigh, symptoms severity by USP score, cognitive impairment by MMSE score and last urodynamic data are recorded. Patient are asked to drink water until they feel a strong need to void, for which they would go to urinate at home. Walk tests are realized in a specific place, with calm and no passage. A chair is placed at each end of the path. Toilets are just next to the hall where they realize the tests. A 10 Meters Walk Test is done during this condition, 3 times (only the intermediate 6 meters are recorded). They can take 30 seconds of rest between each try if necessary. One Timed up and go is done. Patient can use their habitual walking device. Speed walk asking is comfortable for the two test. Next, patient can urinate. 3 post void residual volume with portable echography are done, and the higher is recorded. Patient achieve the same walk tests after urinate, in the same order. They must use the same walking device. Primary outcome is mean gait recorded for 10 meters walk test. Secondary outcome is time for timed up and go test. Individual variability between the 3 10MWT in the two conditions will be study. Influence of age, EDSS, severity of symptoms, MMSE, detrusor overactivity on speed impairment will be study in secondary analysis.

NCT ID: NCT03171272 Completed - Stroke Clinical Trials

Effects of Inspiratory Muscle Training on the Functional Gait Performance of Individuals After Stroke

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

The most commonly observed sequel after stroke is muscle weakness, which can also be identified in respiratory muscles, in the acute and chronic phases, and may compromise the lung function of these individuals. Studies have shown that lower Pimax values are found in non-community ambulators, and gait velocity has been reported as an important indicator of functionality after stroke, with higher gait velocity values associated with greater community participation and better quality of life. This study will test the hypothesis that training of the inspiratory muscles is effective in improving strength and endurance of the inspiratory muscles and functionality, including speed of gait, functional gait perfomarnce, activities of daily living and quality of life with stroke subjects. For this clinical trial, people after stroke will be randomly allocated into either experimental or control/sham groups. The experimental group will undertake training of the inspiratory muscles with the Power Breath Medical Classic device regulated at 50% of the subjects' maximal inspiratory pressure values, five times/week over six weeks, twice a day for 15 minutes, totaling 30 minutes/day. The control group will undertake the same protocol, but the participants will receive the devices with a minimal load, wich corresponds to 1cmH2O. Both groups will participate in the rehabilitation program for 6 weeks. At baseline and post intervention, after the cessation of the interventions, researchers blinded to group allocations will collect the following outcome measures: maximal respiratory pressures, respiratory muscle endurance, functional gait performance, activities of daily living and quality of life. After 12 weeks will collect again maximal inspiratory pressures and functional gait performance.

NCT ID: NCT03135600 Completed - ACL Injury Clinical Trials

The Influence of Running to ACL Deficiency

Start date: April 26, 2017
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the influence of running to kinematic parameters of patients with anterior cruciate ligament.

NCT ID: NCT03135587 Completed - Gait Clinical Trials

The Relationship Between Increasing Loading and Kinematic Parameters

Start date: April 26, 2017
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the influence of increasing loading to kinematic parameters of normal people while walking on the treadmill.

NCT ID: NCT03125434 Terminated - Healthy Volunteers Clinical Trials

Normative Dynamic & Magnetic Spine

NDMS
Start date: April 27, 2017
Phase: N/A
Study type: Interventional

This study aims to describe normal spinal musculoskeletal patterns in healthy adolescents and young adults by using static and dynamic measures. Static informations are obtained from full-spine stereoradiography for skeletal measures and from high-resolution spine muscle MRI for muscular data. Dynamics stability is calculated from 3D gait analysis.

NCT ID: NCT02960932 Completed - Child Development Clinical Trials

Reproducibility Inter-session of the Measurement Elastography of the Passive Stiffness of Medial Beams of Gastrocnemius Muscle of the Hemiplegic Cerebral Child.

ELASTOREPRO
Start date: February 21, 2017
Phase: N/A
Study type: Interventional

Muscles, paretics and spastics, of cerebral palsy children have very early, for growth (three at five aged), every alteration of theirs properties. Gastrocnemius muscle, often reaches on the cerebral palsy, characterised by a modification of the structure (volume decrease) and the elasticity (increase of the passive stiffness). Every alterations of the muscular property have impact clinic and functional important. The many treatments of orthopaedic targeting (lengthening of cast, injections of botulinic toxin), repeated to a multiple recovery during the growth influences the muscular characteristics. There is a real interest to measure the muscular property development during children's growth.

NCT ID: NCT02917850 Withdrawn - Stroke Clinical Trials

Impact of Hip Flexors Isokinetic Strengthening on Gait Capacities in Subacute Stroke Patients

ISOKINETIC
Start date: August 2016
Phase: N/A
Study type: Interventional

Post-stroke patients often present with gait disorders due to several physical impairments. Hip flexor deficit is one of the more prevalent trouble and is associated with gait capacities. This study aims at evaluating the impact of an isokinetic hip flexors strengthening rehabilitation program in the subacute phase after stroke. Patients will be randomized to an intervention group (isokinetic rehabilitation) or a control group (conventional rehabilitation) and assessed at the end of the rehabilitation program, at 3 and at 6 months.

NCT ID: NCT02085954 Completed - Stroke Clinical Trials

Evaluation of a Training in the Walking With Exosquelette

LOKOMAT
Start date: October 2013
Phase: N/A
Study type: Observational

Stroke patients in the investigators rehabilitation unit follow gait trainings with robotic-assistive devices such as Lokomat. Patients able to walk alone are also assessed with 3D gait analysis. The objective of this study is to assess the effects of gait training in Lokomat on biomecanic gait parameters in stroke patients.

NCT ID: NCT02032329 Recruiting - Stroke Clinical Trials

FastFES Gait Training for Stroke Patients: Efficacy of Pre-Commercial Device

Start date: January 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to assess efficacy of a pre-commercial device capable of activating both the ankle plantarflexor and dorsiflexor muscles using electrical stimulating during treadmill-based gait training for stroke patients.

NCT ID: NCT01787721 Terminated - Gait Clinical Trials

Effect of Manipulation of the Ankle Joint on Gait

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

The purpose of this study is to determine if manipulation of the ankle improves some measurable characteristics of how a person walks. The investigators hypothesize that the ankle will be able to bend better after manipulation and thus improve walking speed and reduce differences between the two limbs.