Ignite Creation Date:
2024-05-06 @ 2:22 PM
Last Modification Date:
2024-10-26 @ 1:29 PM
Study NCT ID:
NCT04297527
Status:
UNKNOWN
Last Update Posted:
2020-05-05
First Post:
2020-02-24
Brief Title:
Effect of Mulligan Mobilization in Chronic Non-Spesific Low Back Pain
Sponsor:
Pamukkale University
Organization:
Pamukkale University
Study Overview
Official Title:
Efficacy of Mulligan Mobilization Technique in Chronic Non-Spesific Low Back Pain
Status:
UNKNOWN
Status Verified Date:
2020-05
Last Known Status:
RECRUITING
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:
Fifty five participants diagnosed with CNSLBP will randomized into three groups Group I 18 subjects will receive 15 sessions of Conventional Physiotherapy program CPP 5 times per week Group II 19 subjects will receive 9 sessions of SNAGs and Group III will receive CPP plus SNAGs Outcome measures are pain ROM spinal mobility fear avoidance behaviour and function Measurements will record before after and 6 month after the end of the treatment
Detailed Description:
Inclussion criterias are low back pain for at least 3 months intensity of pain ranges from 3 to 6 according to VAS Exclussion criterias are undergoing surgical operation in the lumbar region or having a surgical indication having an exercise therapy and or physical therapy in the last 1 year a history of trauma involving lumbar region and systemic and inflammatory disease targeting this region participants using corticosteroids for a long time and being pregnantAcording to our criterias 55 participants diagnosed with CNSLBP will randomised into three groups Group 1 will receive Conventional Physiotherapy programme consisting of Hot pack US and TENS applications Group II aill receive Lumbar SNAGS consisting of Lumbar Extension SNAGS in prone SNAGS in lion position and Lumbar flexion SNAGS in sitting techniques Group III will receive 9 sessions of SNAGs and Group III will receive CPP plus SNAGsOutcome measures are pain ROM spinal mobility fear avoidance behaviour and function Measurements will record before after and 6 month after the end of the treatment All treatment groups were treated with the same researcher All assessments were made by another blind researcher three times at before after and 6 month after treatment
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