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Ambulation Difficulty clinical trials

View clinical trials related to Ambulation Difficulty.

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NCT ID: NCT03812406 Recruiting - Pain, Postoperative Clinical Trials

Comparison of FAUCS vs. Misgav Ladach

Start date: August 19, 2018
Phase: N/A
Study type: Interventional

This study aims to compare two techniques for performing a cesarean delivery: Misgav Ladach versus French Ambulatory Cesarean Section (FAUCS). The second techniques has been claimed to reduce post-operative pain, the need for analgesics, and reduce the time for ambulation. Such comparison has not been done so far, and this study will examined if indeed the FAUCS techniques offers any advantages.

NCT ID: NCT03405896 Recruiting - Clinical trials for Ambulation Difficulty

The Validity and Reliability of a Wearable System for Assessing Turning Characteristics.

Start date: August 24, 2017
Phase: N/A
Study type: Interventional

The Validity and Reliability of a Wearable System for Assessing Turning Characteristics.

NCT ID: NCT03341728 Completed - Fall Clinical Trials

The Sensorimotor Locus of Balance Control in Elderly Gait

Start date: October 30, 2017
Phase: N/A
Study type: Interventional

The aging population is at an exceptionally high risk of debilitating falls, contributing significantly to reduced independence and quality of life. It remains extremely challenging to screen for falls risk, and programs designed to mitigate falls risk have only modestly influenced the sizeable portion of the aging population experiencing one or more falls annually. Balance control in standing and walking depends on integrating reliable sensory feedback and on planning and executing appropriate motor responses. Walking balance control is especially dynamic, requiring active and coordinated adjustments in posture (i.e., trunk stabilization) and foot placement from step to step. Accordingly, using a custom, immersive virtual environment, the investigators have shown that sensory (i.e., optical flow) perturbations, especially when applied during walking, elicit strong and persistent motor responses to preserve balance. Exciting pilot data suggest that these motor responses are remarkably more prevalent in old age, presumably governed by an increased reliance on vision for balance control. Additional pilot data suggest that prolonged exposure to these perturbations may effectively condition successful balance control strategies. Founded on these recent discoveries, and leveraging the increase reliance on vision for balance control in old age, the investigators stand at the forefront of a potentially transformative new approach for more effectively identifying and mitigating age-related falls risk. The investigator's overarching hypothesis is that optical flow perturbations, particularly when applied during walking, can effectively identify balance deficits due to aging and falls history and can subsequently condition the neuromechanics of successful balance control via training.

NCT ID: NCT03096197 Recruiting - Spinal Cord Injury Clinical Trials

Exoskeleton and Spinal Cord Stimulation for SCI

Start date: March 30, 2017
Phase: N/A
Study type: Interventional

The overall aim of this project is to assess the effect of combining transcutaneous lumbosacral stimulation (TLS) during Exoskeleton Assisted Walking (EAW) compared to EAW alone without stimulation on walking recovery.

NCT ID: NCT02545205 Terminated - Stroke Clinical Trials

New Technology for Individualised, Intensive Training of Gait After Stroke Study I

HAL-RCT-II
Start date: January 1, 2018
Phase: N/A
Study type: Interventional

The overall purpose of this project is to establish the added value of training with the Hybrid Assistive Limb (HAL) exoskeleton system as part of regular rehabilitation intervention programs after stroke. The aim of this study is to explore if HAL training when combined with conventional training in the subacute stage after stroke may accelerate the recovery of independence in walking when compared to conventional training only and if recovery is related to stroke lateralization?

NCT ID: NCT02545088 Completed - Stroke Clinical Trials

New Technology for Individualised, Intensive Training of Gait After Stroke- Study II

HAL-RCT-II
Start date: October 2015
Phase: N/A
Study type: Interventional

The overall purpose of this project is to establish the added value of training with the Hybrid Assistive Limb (HAL) exoskeleton system as part of regular rehabilitation intervention programs after stroke. The main specific aims are: (i) to compare potential effects on functioning and disability of gait and mobility training long-term after stroke by comparing A) HAL-training combined with conventional rehabilitation interventions to B) conventional rehabilitation interventions without HAL and to C) no intervention.

NCT ID: NCT02410915 Completed - Stroke Clinical Trials

A Comparison Between the Exoskeleton Hybrid Assistive Limb and Conventional Gait Training Early After Stroke

HAL-RCT
Start date: February 2014
Phase: N/A
Study type: Interventional

Overall aim is to evaluate HAL for gait training early after stroke and the effect of HAL on short- and long-term functioning, disability and health compared to conventional gait training as part of an inpatient rehabilitation program early after stroke.

NCT ID: NCT02065284 Completed - Multiple Sclerosis Clinical Trials

Effects of a Home Based Walking Program Using Rhythmic Auditory Stimulation in Patients With Multiple Sclerosis

Start date: February 2014
Phase: N/A
Study type: Interventional

Rhythmic Auditory Stimulation (RAS) is a music therapy technique that provides rhythmic auditory cues (like a beat) to help improve patients' movements, especially when walking. The purpose of this study is to compare the effect on walking performance of a home based walking program (HBWP) with Rhythmic Auditory Stimulation (RAS), to that of a HBWP without RAS, or to RAS without walking exercise. A second part of this study will assess the effects of Rhythmic Auditory Stimulation (RAS) on brain activity in patients with Multiple Sclerosis while performing mental imagery of walking.

NCT ID: NCT01691001 Completed - Clinical trials for Ambulation Difficulty

Effect of Dexmedetomidine on Sevoflurane Requirements and Emergence Agitation in Children Undergoing Ambulatory Surgery

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

Although the aetiology of emergence agitation (EA) derives from multiple factors, it is a frequent side effect of sevoflurane anaesthesia in children. Dexmedetomidine, a potent selective α2-adrenergic agonist, can reduce the doses of hypnotics, opioids, analgesics, and anaesthetics that must be concomitantly administered. This study was conducted to assess the effect of dexmedetomidine infusion on sevoflurane requirements and recovery profiles with EA in children undergoing ambulatory surgery.

NCT ID: NCT01630941 Completed - Osteoarthritis, Hip Clinical Trials

Effects of Denosumab on Periprosthetic Bone After Total Hip Arthroplasty

Start date: August 7, 2012
Phase: Phase 2
Study type: Interventional

The primary objective is to study the effect of Denosumab on Bone Mineral Density, Standardised Uptake Value and bone metabolism in patients with total hip arthroplasty. The primary hypothesis is to demonstrate that Denosumab is superior to placebo.