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

Sponsor
University of Lahore (Other)
Overall Status
Recruiting
CT.gov ID
NCT05174520
Collaborator
(none)
68
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2
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8.4

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: Routine Physical Therapy
  • Other: Muscle Energy Technique
N/A

Detailed 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).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
68 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
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
Actual Study Start Date :
Oct 27, 2021
Anticipated Primary Completion Date :
Jul 1, 2022
Anticipated Study Completion Date :
Jul 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: 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.

Other: Routine Physical Therapy
Routine physical therapy will be provided to group A for 25 minutes thrice a week for 4 weeks.
Other Names:
  • Conventional Physical Therapy
  • Experimental: 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.

    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.

    Outcome Measures

    Primary Outcome Measures

    1. Pain will be assessed by Numeric pain rating scale [1 minute]

      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.

    2. Range of Motion will be assessed by Universal Goniometer [2 minutes]

      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.

    3. Quality of life will be assessed by Medical outcomes study: 20 item Short form survey instrument [8 minutes]

      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.

    4. Functional Disability will be assessed by Oswestry Low Back Pain Disability Index [5 minutes]

      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.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years to 55 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Lahore teaching Hospital Lahore Punjab Pakistan 53700

    Sponsors and Collaborators

    • University of Lahore

    Investigators

    • Study Chair: M Waqar Afzal, Mphil-MSK, University of Lahore
    • Study Director: Syed Asadullah Arslan, Ph.D. PT, University of Lahore

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Hadia Ehsan, Principal investigator, University of Lahore
    ClinicalTrials.gov Identifier:
    NCT05174520
    Other Study ID Numbers:
    • MSPTM02193012
    First Posted:
    Dec 30, 2021
    Last Update Posted:
    Jan 12, 2022
    Last Verified:
    Dec 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Hadia Ehsan, Principal investigator, University of Lahore
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 12, 2022