Ignite Creation Date:
2024-05-11 @ 8:30 AM
Last Modification Date:
2024-10-26 @ 3:29 PM
Study NCT ID:
NCT06407687
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-06-13
First Post:
2024-05-06
Brief Title:
Compare Electrodry Needlig and Dry Needling in Mechanical Low Back Pain
Sponsor:
Riphah International University
Organization:
Riphah International University
Study Overview
Official Title:
Comparative Effects of Electro Dry Needling Versus Dry Needling on Pain Endurance and Range of Motion in Patients With of Quadratus Lumborum Syndrome
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-06
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:
Mechanical low back pain LBP generally results from an acute traumatic event but it may also be caused by cumulative trauma The severity of an acute traumatic event varies widely from twisting ones back to being involved in a motor vehicle collision Mechanical LBP due to cumulative trauma tends to occur more commonly in the workplace and Quadratus Lumborum injury plays an important role in causing MLBP The aim of this study is To compare the effects of Electrical Dry Needling and Dry Needling on pain endurance and range of motion in patients with Quadratus Lumborum Syndrome
Detailed Description:
A Randomized Clinical Trial will be conducted at Ali Afzal Shah Dispensary and Inam ul Haq Clinic Lahore through consecutive sampling technique on 40 patients which will be allocated using simple random sampling and patients will be divided in Group A and B Group A will receive Electrical Dry Needling along with conventional physiotherapy The parameters for Electro dry needling will be needles of 30025 mm 50025 mm sizes Frequency 80-100 Hz Duration 10-30 minutes and intensity as tolerated 1 session per week along with 5 day conventional physiotherapy a week for 4 weeks Group 2 will receive Dry Needling along with conventional Physiotherapy in which parameters will be dry needles will be 30025 and 50025 mm sizes once per week and 5 days of conventional Physiotherapy per week for 4 weeks Data will be analyzed during SPSS software version 25 After assessing normality of data by Shapiro-Wilk test it will be decided either parametric or non-parametric test will be used within a group or between two groups
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