Ignite Creation Date:
2024-07-17 @ 11:43 AM
Last Modification Date:
2024-10-26 @ 3:34 PM
Study NCT ID:
NCT06490354
Status:
RECRUITING
Last Update Posted:
2024-07-08
First Post:
2024-06-29
Brief Title:
Effectiveness of the Use of Lightback in Conventional Football Training
Sponsor:
Universidad Católica de Ávila
Organization:
Universidad Católica de Ávila
Study Overview
Official Title:
Effectiveness of the Use of Lightback in Conventional Football Training Randomised Clinical Trial
Status:
RECRUITING
Status Verified Date:
2024-09
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:
Lightback is a patented device that allows instrumental stretching of the gluteal muscles Football players overload this musculature and this type of device is effective and the costbenefit ratio is high
The intention is to carry out a randomised clinical trial to carry out a study on athletes to see the differences between a group of football players with their normal training and a group of football players with their normal training and the application of lightback beforehand
The variables studied will be sprint speed in 20 and 40m vertical jump height hamstring muscle injuries throughout the season triceps sural injuries throughout the season internal and external hip ROM dorsal flexion ankle ROM
The intention is to carry out a randomised clinical trial to carry out a study on athletes to see the differences between a group of football players with their normal training and a group of football players with their normal training and the application of lightback beforehand
The variables studied will be sprint speed in 20 and 40m vertical jump height hamstring muscle injuries throughout the season triceps sural injuries throughout the season internal and external hip ROM dorsal flexion ankle ROM
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