- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06303388
Effects of Bruegger's Exercises Versus Egoscue Exercise on Lower Cross Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
A randomized control trial will be conducted on patients with lower cross syndrome. A total number of 34 participants will be randomised into two groups with 17 participants in each group. Both groups will receive Hot Packs on the lumbar area for 10 minutes. Group A will receive Conventional Therapy and will follow protocol of Bruegger's Exercise. Group B will follow protocol of the Egoscue exercise. This study aims to decrease pain and hyperlordosis.
Each group will be assessed at baseline which will include pain through NPRS, hyperlordosis through flexicurve ruler and anterior pelvic tilt through pelvic inclinometer. Data from both groups will again be assessed after 4 weeks of intervention.
Protocol of Bruegger's Exercise: Pt. position: Upright sitting on a chair.
- Sit with your buttocks at the edge of a chair.
- Spread your legs apart slightly.
- Turn your toes out slightly.
- Rest your weight on your legs/feet & relax your abdominal muscles.
- Tilt your pelvis forward (i.e. arch your lower back) while lifting your chest up
- Rotate your arms outward while turning your palms up.
- Hold your head high in the air, with a slight arch in the neck.
The patient is to perform this exercise once or twice every 20-30 minutes of prolonged sitting and held in this position for 30-60 seconds. To avoid non-compliance patient will be asked to perform five repetitions of particular exercise with five second hold during their clinical session.
Protocol of Egoscue Exercise The Egoscue group received a total of 10 exercises which includes
- Static back alone and with breathing
- Abdominal contraction while in the static back position
- abductor press
- Overhead extension
- elbow curls on a wall
- Static wall
- Upper spinal twist
- pelvic tilts
- supine groin progressive
- Air bench exercises
Week 1: 3 times with 10 s hold time Week 2: 5 times with 10 s hold time Week 3: 15 times with 10 s hold time Week 4: 20 times with 10 s hold time
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Imran Imjad, Phd
- Phone Number: 03324390125
- Email: imran.amjad@riphah.edu.pk
Study Locations
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Federal
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Rawalpindi, Federal, Pakistan, 44000
- Recruiting
- Pakistan Railway General Hospital
-
Contact:
- Abdul Wasay, MS(SPT)
- Phone Number: 03345056564
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Principal Investigator:
- Azka Batool, MS(OMPT)
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Sub-Investigator:
- Nadia Ishtiaq, MS-OMPT
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria: • Females and males aged between 16 to 65 years
- Participants had to present with low back pain
- Participants had to meet the criteria for lower crossed syndrome indicating tight hip flexors (Modified Thomas test) and erector spinae (visual assessment through toe touching) together with weak glutei (Prone Hip Extension Co-ordination/Strength Test) and abdominals (Trunk Flexion Co-ordination and Strength Test)and thoracic kyphosis.
- Angle of anterior pelvic tilt > 10 degrees
Exclusion Criteria: • Participants who would be undergoing other forms of treatment that may interfere with the study, for the duration of the study, including other manipulative and physical therapies specific to back pain.
- Presence of other conditions that may mimic low back pain, e.g. nerve entrapment.
- Participants taking any medication that may interfere with the results of this study including, pain medication, anti-inflammatory medication, and muscle relaxants.
- Surgery on the back, pelvis, or sacrum is indicated or has previously occurred
- LBP having localised or radiating pain.
- Practiced any kind of exercise or sports activity during the last 6 months.
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: Egoscue Exercise
• The Egoscue exercise comprise of 10 exercises which Included
9.supine groin progressive 10.air bench exercises. |
Egoscue Exercise along with conventional Physiotherapy.
|
|
Active Comparator: Bruegger's Exercise
steps include in Breugger's Exercise
|
Bruegger's Exercise protocol along with conventional Physiotherapy.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Flexicurve Ruler
Time Frame: 12 day
|
The flexicurve ruler (flexible) is commonly used to measure the degree of spinal curvature of the lumbar lordosis in the sagittal plane.
The flexible ruler was placed according to the Youdas method, over spinous processes from T12 to S2 vertebrae.
The ruler was then cautiously removed from the spine and traced onto a plain piece of white paper.
A vertical line was drawn to connect the T12 and S2 landmarks (L line) and together with the maximum width of the lumbar curvature (H line
|
12 day
|
|
Pelvic Inclinometer
Time Frame: 12 day
|
A pelvic inclinometer was used to measure the anterior/posterior inclination of the pelvis of the subjects.
An inclinometer has a 23 Cm length base and two 15 Cm arms in each side that freely move 360 degrees in horizontal plane.
The ends of the arms are placed on the bony landmarks.The subject was asked to stand with the feet shoulder width apart.
Even pressure was applied to both the arms of the inclinometer at anterior superior iliac spine and posterior superior iliac spine, with a bubble in the center the reading was then measured in degrees.
|
12 day
|
|
NPRS
Time Frame: 12 Day
|
Several pain scales are used clinically to evaluate the severity of musculoskeletal pain, one of which is the Numeric Pain Rating Scale (NPRS-11), which is an eleven-point scale in which the endpoints are the extremes of no pain at all (score of 0) and the worst pain the patient has ever experienced (score of 10).
|
12 Day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Modified Thomas Test
Time Frame: 12 day
|
This test was performed with the patient supine and the thighs positioned over the edge of the examining table.
The patient was told to grasp the thigh of the untested limb and pull it toward the chest to flatten the back and stabilise the pelvis, preventing an increase in lumbar lordosis.
A standard stretch position for the iliopsoas muscle is demonstrated with the hip extended and the leg hanging freely with normal knee flexion.
A positive test was indicated if the hip remained flexed against gravity on tested limb.
Additionally, if there was also knee extension on the tested limb then further testing was needed to decide between a tight iliopsoas or rectus femoris muscle.
This was done by passively extending the knee of the tested limb to neutralize the effect of the rectus femoris and find if there was still no change in hip flexion.
|
12 day
|
|
Visual Assessment through toe touching
Time Frame: 12 day
|
The patient was seated on the examining table with the pelvis in a vertical position and the legs extended.
The patient was asked to actively flex foreword in order to bring the forehead to the knees.
The normal functioning of the erector spinae should display an even 'C' shaped curve and a distance of 10cm from the knees to the forehead.
There should be also no knee flexion and involve no pelvic tilting.
Any deviation from these norms indicates shortness of the erector spinae muscles.
|
12 day
|
|
Prone Hip Extension Co-ordination Test
Time Frame: 12 day
|
The patient lay prone and raised the tested thigh into extension with the knee held in an extended position.
The researcher then palpated the lumbar erector spinae and gluteus maximus muscles.
A normal activation sequence was then observed and palpated which involved first the hamstring and gluteus maximus muscles, then the contralateral lumbar erector spinae muscles and lastly the ipsilateral lumbar erector spinae muscles.
A positive test result occurred if the lumbar erector spinae contracted before the gluteus maximus muscles did.
|
12 day
|
|
Trunk Flexion Co-ordination and Strength Test
Time Frame: 12 day
|
The patient lay supine with the arms either behind the neck or forward across the body and knees bent.
The researcher then contacted the patient's heels or positioned a hand under the patient's lumbar spine.
The patient was then asked to complete a posterior pelvic tilt and raise the trunk up until the scapulae cleared the table.
This position was maintained for 2 seconds.
The patient then held the pelvic tilt while lowering their back to the table.
The patient was then instructed to perform 10 repetitions while holding the last repetition for 30 seconds.
A positive test result occurred if the patient could not perform 10 repetitions without the lumbar spine or heels rising off the table.
|
12 day
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Nadia Ishtiaq, MS, Riphah International University
Publications and helpful links
General Publications
- Childs JD, Piva SR, Fritz JM. Responsiveness of the numeric pain rating scale in patients with low back pain. Spine (Phila Pa 1976). 2005 Jun 1;30(11):1331-4. doi: 10.1097/01.brs.0000164099.92112.29.
- Koes BW, van Tulder MW, Thomas S. Diagnosis and treatment of low back pain. BMJ. 2006 Jun 17;332(7555):1430-4. doi: 10.1136/bmj.332.7555.1430. No abstract available.
- Kahl C, Cleland JA. Visual analogue scale, numeric pain rating scale and the McGill pain Questionnaire: an overview of psychometric properties. Physical therapy reviews. 2005;10(2):123-8.
- Waters T. The effect of Bruegger's exercise on chronic low back pain in association with lower crossed syndrome: University of Johannesburg (South Africa); 2014.
- May S, Johnson R. Stabilisation exercises for low back pain: a systematic review. Physiotherapy. 2008;94(3):179-89
- Nourbakhsh MR, Arabloo AM, Salavati M. The relationship between pelvic cross syndrome and chronic low back pain. Journal of back and musculoskeletal rehabilitation. 2006;19(4):119-28.
- Kudchadkar GS, Gurudut P, Welling A. Comparative effect of mat pilates and egoscue exercises in asymptomatic individuals with lumbar hyperlordosis: A randomized controlled trial. Indian Journal of Physical Therapy and Research. 2019;1(2):79-88.
- Sequeira S, Gurudut P, Kage V. Exploring effects of Egoscue versus lumbar stabilisation exercises for lower crossed syndrome on postural stability and hyperlordotic posture correction. Comparative Exercise Physiology. 2023:1-12.
- Vehrs Z. The Effect of Egoscue Corrective Exercises on Chronic Knee and Hip Pain: Brigham Young University; 2014.
- Laxmi V R, G N, V S, G M, Gopinath Y, G T. Efficacy of Janda's approach versus bruegger's exercise in pelvic cross syndrome and its impact on quality of life. International Journal of Research in Pharmaceutical Sciences. 2020;11:1701-6.
- Macintyre NJ, Bennett L, Bonnyman AM, Stratford PW. Optimizing reliability of digital inclinometer and flexicurve ruler measures of spine curvatures in postmenopausal women with osteoporosis of the spine: an illustration of the use of generalizability theory. ISRN Rheumatol. 2011;2011:571698. doi: 10.5402/2011/571698. Epub 2011 Feb 7.
- Khan N, Nouman M, Iqbal MA, Anwar K, Sajjad AG, Hussain SA. Comparing the Effect of Stretching and Muscle Energy Technique in the Management of Lower Cross Syndrome. Pakistan Journal of Medical & Health Sciences. 2022;16(07):31-
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/MS-PT/01721
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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