Ignite Creation Date:
2024-05-06 @ 7:49 PM
Last Modification Date:
2024-10-26 @ 3:14 PM
Study NCT ID:
NCT06145620
Status:
NOT_YET_RECRUITING
Last Update Posted:
2023-12-05
First Post:
2023-11-17
Brief Title:
Effects of a Prehabilitation Program in Patients Undergoing Lumbar Radiculopathy Surgery
Sponsor:
Cardenal Herrera University
Organization:
Cardenal Herrera University
Study Overview
Official Title:
Effects of a Prehabilitation Program Based on Therapeutic Exercise Back Care Education and Neuroscience Pain Education in Patients Undergoing Lumbar Radiculopathy Surgery
Status:
NOT_YET_RECRUITING
Status Verified Date:
2023-11
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 purpose of the following study is to analyze the effects of a prehabilitation program based on therapeutic exercise back care education and pain neuroscience education through the visualization of videos compared to standardized written therapeutic exercise in patients undergoing lumbar radiculopathy surgery
Detailed Description:
So far there are no previous studies that analyze the effects of a prehabilitation program including therapeutic exercise back care education and pain neuroscience education through the visualization of videos in patients undergoing lumbar radiculopathy surgery
This is a multicenter randomized clinical trial aimed at analyzing the effects of a 4 weeks prehabilitation program based on video visualization versus the performance of standardized written exercises in patients undergoing lumbar radiculopathy surgery
This is a multicenter randomized clinical trial aimed at analyzing the effects of a 4 weeks prehabilitation program based on video visualization versus the performance of standardized written exercises in patients undergoing lumbar radiculopathy surgery
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