Ignite Creation Date:
2024-06-16 @ 11:52 AM
Last Modification Date:
2024-10-26 @ 3:32 PM
Study NCT ID:
NCT06459804
Status:
COMPLETED
Last Update Posted:
2024-06-14
First Post:
2024-06-11
Brief Title:
Effects of Electro Dry Needling Versus Dry Needling in Levator Scapulae Syndrome
Sponsor:
Riphah International University
Organization:
Riphah International University
Study Overview
Official Title:
Effects of Electro Dry Needling Versus Dry Needling on Pain Muscle Strength and Range of Motion in Patients With Levator Scapulae Syndrome
Status:
COMPLETED
Status Verified Date:
2024-10
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 neck pain is posteriorly occurring non-specific pain that originates from the superior nuchal line and extends to the first thoracic vertebrae It is exacerbated by sustained neck postures neck movements or cervical muscle palpation The aim of study will be to compare the effects of Electro Dry Needling and Dry Needling on pain muscle strength disability and range of motion in patients with Levator Scapulae Syndrome
Detailed Description:
A Randomized Clinical Trial will be conducted at Shalamar Hospital SIHS Physiotherapy Clinic Lahore through convenience sampling technique on 30 patients which will be allocated using simple random sampling through sealed opaque enveloped into Group A and Group B Group A will receive Electro Dry Needling along with conventional physiotherapy in which parameters for Electro dry needling will be needles of 30025 mm 50025 mm sizes Frequency 80-100 Hz Duration 10-20 minutes and intensity as tolerated and Group B will receive Dry Needling along with conventional Physiotherapy in which parameters will be dry needles will be 30025 and 50025 mm sizes Standard Physiotherapy will include a Hot pack 10 min Stretching of levator scapulae 3 times with 30 second hold and Scapular stabilization exercises 10 times with 5 second holdThere will be 3 sessions per week Needling in both groups will be for performed 2 times per week for total 3rd week of treatment comprising of 6 sessions 3rd session will comprise of standard physical therapy Pre and Post treatment measures will be recordedOutcome measures will be conducted through pain muscle strength disability and range of motion questionnaire Data will be analyzed during SPSS software version 25After assessing the normality of data by the Shapiro-Wilk test it will be decided whether a 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