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Gait Analysis clinical trials

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NCT ID: NCT05957783 Completed - Cerebral Palsy Clinical Trials

Changes in Upper Limb Kinematics in Children With Cerebral Palsy After Lower Limb Surgery

Start date: January 3, 2021
Phase:
Study type: Observational

İntroduction The upper limb can be involved in children with cerebral palsy (CP), while the lower limb is more commonly affected. Little is known regarding the alterations in the upper limb kinematics after the orthopedic surgery of the lower extremity during gait. This study aimed to evaluate the differences in the upper limb kinematics in children with CP between preoperative and postoperative parameters.

NCT ID: NCT05538221 Completed - Gait Analysis Clinical Trials

Reliability of a Gait Analysis System

Start date: October 20, 2022
Phase:
Study type: Observational

Gait disturbances can be observed in all age groups, and may be due to different conditions, such as advanced age, stroke, head trauma, spinal cord injury, cerebral palsy, myelomeningocele, among others. The aforementioned gait disorders are associated with an increased risk of falls (which can cause major fractures or head trauma), decreased mobility, loss of independence, cardiovascular pathology, and decreased quality of life. In order to improve a given abnormal gait pattern, an objective assessment of gait is necessary. There are several methods to carry out gait evaluations, like Instrumented Gait Analysis (High cost, time-consuming, qualified professionals needed) and the ones based on observation (limited reliability and validity). An alternative, is the use of video-based systems. SILEMA (Computer System for Gait Study Laboratories in Argentina) is a video-based low-cost gait analysis system that measures temporo-spatial (speed, step length, cadence, stance and swing times) and joint kinematic (Hip, Knee, Ankle) parameters. Its reliability has not been reported yet; thus the primary aim of this study is to determine both the "intra-evaluator" (same evaluator, different sessions) and "inter-evaluator" (same session, different evaluators) reliability.

NCT ID: NCT04791605 Completed - Hip Fractures Clinical Trials

Gait Pattern Between a Cemented and Non-cemented Femur Stem

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

Acute cervical femoral neck fracture patients randomized to either cemented or non-cemented stem. The investigators used gait analysis to evaluate if patients operated with a cemented stem showed more favourable hip kinematics and kinetics when compared with a group of patients operated with a non-cemented stem.

NCT ID: NCT04788719 Completed - Clinical trials for Total Hip Arthroplasty

Pre and Postoperative Gait Analysis of Randomized Patient to 2 Different Cement Fixation Methods

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

The primary goal of Total Hip Replacement (THR) surgery in the treatment of hip osteoarthritis is to reduce pain and restore hip function in order to increase patient mobility and quality of life. Two different cement fixation methods are used in order to insert THR implants. This will be done before and after surgery in 2 groups randomized to either of 2 cement fixation methods. Gait analysis preoperative and 2 year after surgery.

NCT ID: NCT04529642 Completed - Stroke Clinical Trials

Is the 6-Minute Walking Test Combined With an IMU Useful in Stroke Rehabilitation Assessment?

Start date: February 1, 2019
Phase:
Study type: Observational

This Observational study aims at the evaluation of stroke subjects with an inertial measurement unit (IMU) during the execution of a 6-Minute Walking test, to evaluate the associations between the kinematic parameters retrieved trough an IMU and the classical outcome scales. Moreover compare the stroke subjects with age-matched healthy subjects, and detect the differences of gait kinematic.

NCT ID: NCT04434313 Completed - Stroke Clinical Trials

Treatment of Hemiparetic Gait Impairments Using Telehealth With the Moterum iStride Solution™

Start date: April 20, 2020
Phase: N/A
Study type: Interventional

The objective of this research is to investigate the feasibility of delivering gait treatment using the Moterum iStride Solution™ to individuals with hemiparetic gait impairments using a telemedicine modality, the Moterum Digital Platform.

NCT ID: NCT04230733 Completed - Clinical trials for Lumbar Disc Herniation

Pelvis Displacement and Gait Indicators in Patient With Lumbar Disc Herniation

Start date: August 20, 2019
Phase:
Study type: Observational

The purpose of this study is to investigate the correlation between pattern of gait and pelvic displacement in patients with lumbar disc herniation.

NCT ID: NCT03965715 Completed - Gait Analysis Clinical Trials

An Ankle-foot Orthosis Improves Gait Performance and Satisfaction in Stroke Patients

Start date: April 19, 2017
Phase: N/A
Study type: Interventional

All participants were at least 6-month post-stroke and had unilateral limb involvement (8 right/4 left). The main inclusion criteria in selection of the participants in this study were as follows :(1) First stroke (2) At least 6 months post stroke (3) Able to stand for at least one minute without any assistive devices (4) Able to walk for at least 10 meters. All participants were instructed to walk with bare foot or with ankle-foot orthoses(AFOs) separately under gait detection of the motion capture system. Participants were further instructed to complete the 10 Meter Walk Test at a comfortable speed with BF or with AFOs separately. All participants were provided with sufficient rest between each trial. Patient demographics such as lower limb Brunnstrom stage and Modified Ashworth Scale (MAS) score were examined and recorded by experienced therapist. The satisfaction and outcome were measured by the Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST) and SF-36. The kinematic and kinetic data were collected by Motion Analysis system.

NCT ID: NCT03898544 Completed - Clinical trials for Knee Arthroplasty, Total

Gait Kinematics After Primary Total Knee Arthroplasty (TKA) Versus Revision TKA

Stryker-KneeKG
Start date: March 18, 2019
Phase:
Study type: Observational

The functional outcomes after TKA are satisfying with a full recovery at 6 months - 1 year. Nevertheless, the revisions of TKA have often lower functional results than primary TKA with a long delay of recovery. The Stryker TKA present the same device for primary TKA and for revision. The aim of this study is to compare the gait kinematics at 6 months after primary Stryker TKA or Revision Stryker TKA to assess if the objective outcomes are similar with this device.

NCT ID: NCT01620021 Completed - Gait Analysis Clinical Trials

Feasibility of Wearable Sensors to Determine Gait Parameters

Start date: April 2011
Phase: N/A
Study type: Observational

Hypotheses: • A wearable sensor system can be used to accurately monitor three common gait parameters: gait speed, stride length, and torso motion. Objectives: This study will examine the feasibility of using wearable sensors to monitor common gait parameters: gait speed, stride length and torso motion. A wearable sensor system of 8 commercially available inertial measurement units (IMU) will be composed. These sensors will work in unison to monitor the gait parameters. Technical Objectives - Gather information on commercially available IMUs - Use computer software to monitor and record data from IMUs - Develop an algorithm that can monitor volunteer gait speed, stride length and torso motion - Develop a graphical algorithm that compares healthy patient data to potential mild traumatic brain injury (mTBI ) candidates - Determine if there is a potential for mTBI determination using the wearable sensors - Accurately validate the wearable sensor system to the gait parameters measured using a Vicon motion analysis system