Viewing Study NCT06594653



Ignite Creation Date: 2024-10-26 @ 3:40 PM
Last Modification Date: 2024-10-26 @ 3:40 PM
Study NCT ID: NCT06594653
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: None
First Post: 2024-08-05

Brief Title: Evaluation of Outcomes of Robotics Rehabilitation in Cerebral Palsy
Sponsor: None
Organization: None

Study Overview

Official Title: Evaluation of Outcomes Related to Walking in a Rehabilitation Program Supported by Robotics Lokomat in Children Suffering from Congenital and Acquired Brain Injuries
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: LK
Brief Summary: The use of robotic devices in rehabilitation programs can improve walking patterns by reorganizing joint kinematics This study aims to quantify the effects of a rehabilitation program supported by the Lokomat Hocoma robotic device on walking in children and young people with movement disorders considering different levels of impairment
Detailed Description: Cerebral Palsy is one of the most common neuromotor disorders in pediatric age characterized by permanent movement and posture impairments often affecting walking In recent decades advancements in robotics have revolutionized rehabilitation Studies have shown that combining conventional physiotherapy with robotic rehabilitation tools offers greater benefits in patient recovery At the IRCCS Eugenio Medea a robotic rehabilitation program using the Lokomat Hocoma has been implemented for several years to improve walking in children and young people with walking disorders The investigators hypothesize that robotic devices can enhance walking ability eg speed stride length and reorganize joint kinematics This study aims to quantify the effects of this treatment based on the level of impairment

Study Oversight

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