Viewing Study NCT06008743



Ignite Creation Date: 2024-05-06 @ 7:25 PM
Last Modification Date: 2024-10-26 @ 3:06 PM
Study NCT ID: NCT06008743
Status: RECRUITING
Last Update Posted: 2023-08-24
First Post: 2023-08-15

Brief Title: Model-informed Patient-specific Rehabilitation Using Robotics and Neuromuscular Modeling
Sponsor: University of Delaware
Organization: University of Delaware

Study Overview

Official Title: Model-informed Patient-specific Rehabilitation Using Robotics and Neuromuscular Modeling
Status: RECRUITING
Status Verified Date: 2023-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Stroke is the third leading cause of death and the primary cause of long-term disability in the United States affecting approximately 795000 people each year Hemiparesis or unilateral weakness is common after stroke and responsible for changes in muscle activation and movement patterns as well as declines in walking speed It has been shown that increased walking speed directly corresponds to a higher quality of life in older adults and therefore is often the goal of motor rehabilitation after stroke However there is no consensus on the best method for improving walking function after stroke and the results of post-stroke gait studies vary widely across sites and studies Walking is one of the humans most important functions that serve survival progress and interaction The force between the foot and the walking surface is very important Although there have been many studies trying to understand this there is a need for the development of a system that can advance research and provide new functionality In this work we will conduct a series of studies that attempt to analyze human gait and adaptations from different perspectives
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None