Viewing Study NCT03690726



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Last Modification Date: 2024-10-26 @ 12:55 PM
Study NCT ID: NCT03690726
Status: COMPLETED
Last Update Posted: 2020-12-29
First Post: 2018-09-20

Brief Title: The Effects of rTMS in Rehabilitation Following Spinal Cord Injury
Sponsor: Spinal Cord Injury Centre of Western Denmark
Organization: Spinal Cord Injury Centre of Western Denmark

Study Overview

Official Title: The Effects of Systematic Repetitive Transcranial Magnetic Stimulation in Rehabilitation After Incomplete Spinal Cord Injury Neuromuscular Adaptations and Recovery of Lower Limb Muscle Strength
Status: COMPLETED
Status Verified Date: 2020-12
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: The project will investigate whether repetitive transcranial magnetic stimulation rTMS can be used to potentiateprime spinal cord injured patients nervous systems for more intense rehabilitation exercise of longer duration - thus leading to greater recovery of motion function The technique in which a magnetic coil is positioned above the scalp and forms a magnetic field that activates the desired center of the brain eg motor cortex is used in clinical practice for the treatment of a number of disorders However although a combination of rTMS and gait training in SCI patients previously has proven beneficial it is unknown whether additional functional gains can be achieved by combining rTMS and supervised high-intensity resistance training

In this project 30 newly-admitted patients will be recruited and randomized to receive either active rTMS and strength training n 15 or sham imitated rTMS strength training in parallel with standard care The investigators hypothesize that the active rTMS group will have superior gains in locomotor function and muscle mass compared to the sham group
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