Viewing Study NCT06485830



Ignite Creation Date: 2024-07-17 @ 11:02 AM
Last Modification Date: 2024-10-26 @ 3:33 PM
Study NCT ID: NCT06485830
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-07-03
First Post: 2024-06-18

Brief Title: Neural Mobilization and Cerebral Palsy
Sponsor: University of Seville
Organization: University of Seville

Study Overview

Official Title: Effect of Neural Mobilization Compared to Conventional Physical Therapy in Children Diagnosed With Cerebral Palsy A Pragmatic Approach
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-07
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: NEUROREHAB
Brief Summary: Objective To assess the effect of neural mobilization applied to the lower limbs compared to conventional physical therapy in children diagnosed with Cerebral Palsy Using the International Classification of Functioning Disability and Health the investigators will try to evaluate the impact of the intervention in aspects related with structure activity and participationThis project will mainly focus on the structure dimension More specifically the investigators aim to observe if a treatment protocol designed to modify the structure egthe sciatic nerve using neural mobilization techniques will evoke changes not only in the structural dimension but also will be able to modify the activity and participation dimensions

Design A single blinded randomized clinical trial the evaluator will remain blinded to treatment allocation group will be conducted The experimental group will receive an intervention consisting on the use of neurodynamic mobilization procedures of the lower limb and participants in the control group will undergo a conventional physical therapy intervention stretching mobilization without the use of neural mobilization

Subjects Participants will be aged between 5 and 18 years and with a confirmed diagnosed of Cerebral Palsy with the presence of spasticity in the lower limbs

Methods Participants will be randomly allocated into two groups experimental or control group The primary outcome will be the range of motion flexion and extension of the hip knee and ankle Secondary outcomes will include gross motor function pain intensity muscle stiffness muscle tension and functional measures
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