Comparative Effects of Muscle Energy Technique and Routine Physical Therapy on Quadratus Lumborum in Patients With Chronic Low Back Pain

Chronic Low-back Pain Clinical Trial

Official title:

Comparative Effects of Muscle Energy Technique and Routine Physical Therapy on Quadratus Lumborum in Patients With Chronic Low Back Pain: A Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05174520
• Other study ID #: MSPTM02193012
• Status: Completed
• Phase: N/A
• Start date: October 27, 2021
• Est. completion date: July 1, 2022

Study information

• Verified date: August 2022
• Source: University of Lahore
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

•Null hypothesis: There is no difference in effects of Muscle Energy Technique and Routine Physical Therapy on Quadratus Lumborum in patients with chronic low back pain. •Alternative hypothesis: There is difference in effects of Muscle Energy Technique and Routine Physical Therapy on Quadratus Lumborum in patients with chronic low back pain.

Description:

The purpose of the study is to compare the effects of Muscle Energy Technique and Routine Physical Therapy on Quadratus Lumborum in patients with chronic low back pain on Pain, Range of Motion, Quality of Life and Functional Disability. The study procedure will be explained to the patients and informed written consent will be obtained from those patients who will be willing to participate in the study. Quadratus Lumborum tightness will be assessed using side bending test. Those fulfilling the requirement of inclusion criteria will be indiscriminately separated into 2 groups. NPRS, Oswestry Disability Index, SF-20 and goniometer will be used to collect data. Total 68 participants will be recruited in the study. Routine Physical therapy will be provided to group A. Reciprocal inhibition Muscle Energy Technique on quadratus lumborum along with Routine Physical Therapy will be performed on group B. Both group will receive interventions three sessions in a week for 4 consecutive weeks. Assessment of Pain, Range of motion, Quality of Life and Functional Disability will be assessed by using goniometer, NPRS, Oswestry Disability Index and SF-20 Questionnaire respectively for both groups at the baseline, end of 6th session (2nd week) and end of 12th session (4th week) and follow up will be obtained after 1 month (8th week).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 68
• Est. completion date: July 1, 2022
• Est. primary completion date: July 1, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 30 Years to 55 Years

Eligibility

Inclusion Criteria:

• Both genders of age 30 to 55 year.
• Patients with pain for at least three months or more (chronic stage).
• Patients having score of at least 3 on 0-10 points(NPRS).
• Diagnosed patients of low back pain.
• Non-radicular low back pain.
• Quadratus Lumborum tightness by physical test i.e. side bending test.

Exclusion Criteria:

• Pregnant females.
• Lumbar radiculopathy.
• Any spinal pathology i.e. infectious disease and fracture.
• Any congenital deformity of spine, upper and lower extremities.
• Systemic illnesses i.e. cardiovascular disorders, respiratory disorders etc.
• History of surgery of hip, pelvis, lumbar spine, disc herniation.

Related Conditions & MeSH terms

• Back Pain
• Chronic Low-back Pain
• Low Back Pain

Intervention

Other:
• Routine Physical Therapy
Routine physical therapy will be provided to group A for 25 minutes thrice a week for 4 weeks.
• Muscle Energy Technique
Muscle Energy technique along with Routine physical therapy will be provided to group B for40 minutes thrice a week for 4 weeks.

Locations

Country	Name	City	State
Pakistan	University of Lahore teaching Hospital	Lahore	Punjab

Sponsors (1)

Lead Sponsor	Collaborator
University of Lahore

Country where clinical trial is conducted

Pakistan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain will be assessed by Numeric pain rating scale	Pain will be measured using 11 point Numeric Pain rating scale (NPRS). 0 score represents no pain, 1-3 score represents mild pain, 4-6 represents moderate pain and 7-10 represents severe pain.	1 minute
Primary	Range of Motion will be assessed by Universal Goniometer	Lumbar flexion, extension and side bending range of motion will be measured using Universal Goniometer. Normal lumbar flexion range is 60 degrees, extension range is 25 degrees, and right and left side bending range is 25 degrees.	2 minutes
Primary	Quality of life will be assessed by Medical outcomes study: 20 item Short form survey instrument	The SF-20 measure contains three dimensions about function (physical, social and role) and well-being (mental health, health perception and pain). score between 75- 100 leveled as good quality of life of low back pain patients, Average QOL marked when QOL score between 50-74, and QOL score between 0-49 leveled as poor QOL.	8 minutes
Primary	Functional Disability will be assessed by Oswestry Low Back Pain Disability Index	Oswestry disability index is a validated, 10-point patient-reported outcome questionnaire. • 0% to 20% is scored as minimal disability. • 21%-40% is scored as moderate disability. • 41%-60% is scored as severe disability. • 61%-80% is scored as crippled. • 81%-100% scored as bedbound patients.	5 minutes