Viewing Study NCT06521294



Ignite Creation Date: 2024-10-26 @ 3:36 PM
Last Modification Date: 2024-10-26 @ 3:36 PM
Study NCT ID: NCT06521294
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-07-16

Brief Title: Mulligan SNAG Technique in Individuals With Lumbar Intervertebral Disc Protrusion
Sponsor: None
Organization: None

Study Overview

Official Title: Effect of the Mulligan SNAG Technique on Structure of Intervertebral Disc and Physical Functioning in Individuals With Lumbar Intervertebral Disc Protrusion A Randomized Controlled Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-10
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: None
Brief Summary: This study aimed to examine the effects of the Mulligan SNAG mobilization technique applied in addition to conventional physiotherapy on the structure of the intervertebral disc and physical functioning in patients diagnosed with low back pain due to lumbar intervertebral disc protrusion 38 volunteer patients will participate in the study The participants will be randomized as an interventional and control gropus
Detailed Description: Participants will be treated 3 days a week for 4 weeks The session duration will be 40-45 minutes Visual analog scale-VAS oswestry disability index magnetic imaging-MRI assessment functıonal independence scale-FIM Tampa kinesiophobia scale one leg stand test sit-stand test 10-meter walking test cadence Nottingham health profile will be used to assses the participants in the two groups All participants will be evaluated in the 5th week of the study The program includes physical therapy session Hot packed trans cuteneal electric stimulation therapeutic ultrasound and therapautic exercises and the Mulligan SNAG mobilization technique

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