- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05473416
Comparing the Effects of Pilates and McKenzie in Power Looms Workers Having Nonspecific Chronic Low Back Pain
Comparing the Effects of Pilates (Pelvic Tilt) and McKenzie Back Extension Exercises in Power Loom Workers Having Non-specific Chronic Low Back Pain
Study Overview
Status
Intervention / Treatment
Detailed Description
The purpose of this study is to check and compare the effects of McKenzie back extension exercise and Pilates pelvic tilt exercise on power looms workers having nonspecific chronic low back pain. To check the effects of these interventions on pain, disability, and anterior pelvic tilt angle.
In this study pain intensity of the subjects will be noted via a numeric pain rating scale. Pain will be measured at baseline, after 2 weeks and 4 weeks of intervention.
In this study disability of the patients will be measured via Quebec back pain disability scale. Disability will be measured at baseline, after 2 weeks and 4 weeks of intervention.
In this study, a goniometer will be used to measure the anterior pelvic tilt angle. Anterior pelvic tilt angle will be measured at baseline, after 2 weeks and 4 weeks of intervention.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
-
Faisalabad, Punjab, Pakistan, 38000
- Dr Hafiz Almas PT
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age of the participants between 35-45 years.
- Only male workers diagnosed with nonspecific chronic low back pain.
- Power looms workers; Operator of power looms, working 12 hours per day.
- Low back pain for more than three months.
- Power looms workers with pain intensity on NPRS ranges from mild to moderate.
- Anterior pelvic tilt angle more than normal 13º±4.9º, anteriorly tilt to 18º to 25º.
Exclusion Criteria:
- Serious spinal pathology like tumors.
- Any inflammatory diseases.
- History of spinal surgery.
- Neurological disorder.
- Pain due to any systemic diseases.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 1- McKenzie (Group A)
Back extension exercise.
Total 10 repetitions in 1 set.
Total 3 sets in a session.
Total 3 sessions in a week.
Total 12 sessions in a month.
|
McKenzie's back extension exercise consists; start with your belly facing down on the mat.
Angle your legs in line with your hips, point your toes, and breathe into the next movement.
Gently bending your elbows, push yourself up off the floor, until you feel the extension in your back.
Be mindful not to lock your elbows as you support your weight with your hands and wrists for 10 seconds.
Take deep inhales and exhales as you move in and out of the pose.
Patients will be performed these activities under the supervision of physiotherapist.
Postural guidelines + proper lifting technique + stretch break Rest
Other Names:
|
|
Experimental: 2- Pilates (Group B)
Pelvic tilt exercise Total 10 repetitions in 1 set.
Total 3 sets in a session.
Total 3 sessions in a week.
Total 12 sessions in a month.
|
Postural guidelines + proper lifting technique + stretch break Rest
Other Names:
Pilates pelvic tilt exercise consists; lie with your back on the floor in a neutral position with your legs bent and toes facing forward.
Pull your belly button in toward your spine, pushing your pelvis up toward the ceiling.
Tighten your gluteus and hip muscles as you tilt your pelvis forward.
Hold for 10 seconds.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain intensity
Time Frame: one month
|
In this study pain intensity of the subjects will be noted via numeric pain rating scale.
The reading of NPRS is in number from 0 to 10 where 0 mean no pain, 10 means worst pain, 1-3 indicate mild pain, 4-6 present moderate pain, and 7-10 means severe pain.
Patient tell us in numeric form how much he feels pain for example patient tell us he has 4 pain; its mean patient has moderate pain.
|
one month
|
|
Disability index
Time Frame: one month
|
In this study disability of the patients will be measured via Quebec back pain disability scale.
The 20-item Quebec back pain Disability Scale for Back Pain was created to measure degree of functional disability in people who have low back pain.
The scale is a dependable and valid measurement used to evaluate each patient's improvement during treatment or rehabilitation programmers.
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one month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anterior pelvic tilt angle abnormailty
Time Frame: one month
|
In this study goniometer was used to measure the anterior pelvic tilt angle of the power loom workers.
Goniometer has three parts the body, stationary arm, and the mobile arm.
To check the anterior pelvic tilt angle in subjects the body of the goniometer was placed on the anterior superior iliac spine horizontally, mobile arm was moved to the posterior superior iliac spine and noted the reading displayed on the goniometer.
|
one month
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hafiz Muhammad Almas Sabir Muhammad Sabir Ali, MS OMPT, The University of Faisalabad
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HAFIZ MUHAMMAD ALMAS SABIR
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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