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

NCT ID: NCT05174520

Last Updated: 2022-08-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

68 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-10-27

Study Completion Date

2022-07-01

Brief Summary

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•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.

Detailed Description

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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).

Conditions

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Chronic Low-back Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Routine Physical Therapy group

Routine physical therapy group includes thermotherapy for 10 mins, transcutaneous electrical nerve stimulations for 10 mins. Exercises such as: Pelvic tilts, bridging exercise, William flexion exercises and stretching will be performed for 7-10 repetitions.

Treatment duration will be 25 minutes.

Group Type ACTIVE_COMPARATOR

Routine Physical Therapy

Intervention Type OTHER

Routine physical therapy will be provided to group A for 25 minutes thrice a week for 4 weeks.

Experimental group

Experimental group includes 6-7 repetitions of Muscle energy technique on Quadratus Lumborum muscle and Routine physical therapy, i.e Thermotherapy, transcutaneous electrical nerve stimulations, Pelvic tilts, bridging exercise, William flexion exercises and stretching will be performed for 7-10 repetitions.

Treatment duration will be 40 minutes.

Group Type EXPERIMENTAL

Muscle Energy Technique

Intervention Type OTHER

Muscle Energy technique along with Routine physical therapy will be provided to group B for40 minutes thrice a week for 4 weeks.

Interventions

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Routine Physical Therapy

Routine physical therapy will be provided to group A for 25 minutes thrice a week for 4 weeks.

Intervention Type OTHER

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.

Intervention Type OTHER

Other Intervention Names

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Conventional Physical Therapy

Eligibility Criteria

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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.
Minimum Eligible Age

30 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Lahore

OTHER

Sponsor Role lead

Responsible Party

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Hadia Ehsan

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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M Waqar Afzal, Mphil-MSK

Role: STUDY_CHAIR

University of Lahore

Syed Asadullah Arslan, Ph.D. PT

Role: STUDY_DIRECTOR

University of Lahore

Locations

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University of Lahore teaching Hospital

Lahore, Punjab Province, Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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MSPTM02193012

Identifier Type: -

Identifier Source: org_study_id

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