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Gait Disorders clinical trials

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NCT ID: NCT06453863 Not yet recruiting - Parkinson Disease Clinical Trials

Effects of Biofeedback Footwear in Parkinson's Disease: Assessment of Functional Motor Abilities and Locomotion

Start date: July 1, 2024
Phase: N/A
Study type: Interventional

The study aims to verify whether the use of a specific footwear providing increased plantar feedback (plantar feedback shoes) could improve gait parameters, postural control and functional performances in people with Parkinson's disease. Specifically, the aims are: - To evaluate the acute effect of plantar feedback shoes, by comparing gait, functional and postural performances in three conditions: neutral shoes, barefoot, and plantar feedback shoes; - To evaluate the effect of four weeks of plantar feedback shoes, on gait, functional and postural performances. Participants will undergo a comprehensive neurological examination, with administration of disease-specific scales (UPDRS III part 3, NFOG-q, LEDD, DASS-21). At each assessment the participants will perform an inertial gait analysis, a static posturography, and will undergo functional capacity assessments (TUG, 2MWT, 5-STST, 10- mFW).

NCT ID: NCT02134158 Completed - Gait Disorders Clinical Trials

Impact of tDCS on Locomotion and Equilibrium in Hemiplegic Patients

HEMILOCOSTICOR
Start date: July 10, 2014
Phase: Phase 4
Study type: Interventional

The aim of this trial is to quantify the improvement of locomotion and equilibrium induced par tDCS in anode polarity position in post stroke hemiplegic patients.

NCT ID: NCT01006967 Completed - Gait Disorders Clinical Trials

ActiveStep Comparative Effectiveness Trial

RACE
Start date: November 2009
Phase: N/A
Study type: Interventional

The investigators are conducting a multi-center randomized prospective trial comparing a standard physical therapy gait and balance program with a gait and balance program that includes the ActiveStep™ treadmill. Subjects will be randomized to either have the ActiveStep™ as part of their therapy or to have their therapy without it. Data will be gathered from session notes, medical records and short interviews with the subjects at baseline and every 3 months over the telephone for the duration of the study.

NCT ID: NCT00768378 Completed - Vestibular Diseases Clinical Trials

Safety and Efficacy Study of BrainPort® Balance Device in Peripheral Vestibular Dysfunction.

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

The purpose of this study is to assess the safety and efficacy of the BrainPort balance device in improving balance and gait as measured by clinically accepted standardized balance assessments in subjects with peripheral vestibular dysfunction.