Ignite Creation Date:
2024-10-26 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 3:36 PM
Study NCT ID:
NCT06534853
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-07-30
Brief Title:
Comparison of Post Facilitation Stretch Versus Reciprocal Inhibition in Quadratus Lumborum Syndrome a Randomized Controlled Trial
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Comparison of Post Facilitation Stretch Versus Reciprocal Inhibition in Quadratus Lumborum Syndrome a Randomized Controlled Trial
Status:
RECRUITING
Status Verified Date:
2024-07
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 is a randomised control trial and the purpose of this study is to determine the effects Post facilitation stretch versus reciprocal inhibition on pain lumbar range of motion apparent leg length discrepancy and lumbar lordotic angle in Quadratus Lumborum Syndrome
Detailed Description:
The purpose of this study is to determine the difference between Post facilitation stretch versus reciprocal inhibition on pain lumbar range of motion apparent leg length discrepancy and lumber lordotic angle in Quadratus Lumborum Syndrome
The individual of Age 18-35 years among both genders who experiences pain of 3 on NPRS from at least 3 months and whose pain decreases on supine lying along with any two of the following findings positive of quadratus lumborum on physical examination ie Taut bands Local tenderness Patients pain recognition Pain referral to greater trochanter Local twitch response Jump sign will be recruited in the study as patients of Quadratus lumborum syndrome
Pain levels will be assessed using the Numeric Pain Rating Scale NPRS Inclinometer will be used for measuring lumber ranges To assess apparent leg length discrepancy measuring tape will be used The lumbar lordotic angle will be measured using 60 cm flexible ruler Participants of interest would be approached and explained about the research Informed written consent will be taken It is a non-blinded study and randomization will be done through sealed envelope Both groups will receive conventional intervention Additionally Group A will receive quadratus lumborum post facilitation stretches while Group B will receive Reciprocal inhibition Baseline and post intervention scores would be recorded for both groups
The individual of Age 18-35 years among both genders who experiences pain of 3 on NPRS from at least 3 months and whose pain decreases on supine lying along with any two of the following findings positive of quadratus lumborum on physical examination ie Taut bands Local tenderness Patients pain recognition Pain referral to greater trochanter Local twitch response Jump sign will be recruited in the study as patients of Quadratus lumborum syndrome
Pain levels will be assessed using the Numeric Pain Rating Scale NPRS Inclinometer will be used for measuring lumber ranges To assess apparent leg length discrepancy measuring tape will be used The lumbar lordotic angle will be measured using 60 cm flexible ruler Participants of interest would be approached and explained about the research Informed written consent will be taken It is a non-blinded study and randomization will be done through sealed envelope Both groups will receive conventional intervention Additionally Group A will receive quadratus lumborum post facilitation stretches while Group B will receive Reciprocal inhibition Baseline and post intervention scores would be recorded for both groups
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