- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04801212
The Effects of Lumbar Stabilization Exercises With and Without Jaw Movements in Non-specific Low Back Pain.
May 3, 2023 updated by: Muhammad Khan, University of Lahore
Core stability strength & coordination is necessary to perform smooth & coordinated upper & lower extremity movements & function.
Altered core stability muscle strength, coordination & poor motor control can cause low back pain (LBP).
Physical therapists especially those working with children having neurodevelopmental problems or adults with neurological disorders such as stroke are aware of the concepts of global movements.
In this concept, alterations in one body segment may bring changes in other body segments.
In neurological rehabilitation, the concept of Neuro-Developmental Technique (NDT) introduced by Bobath got worldwide recognition.
This concept states that there are specific key points in the neck, & shoulders that can facilitate normal movements by enhancing the activity of core musculature in functional movements for instance, sit to stand & walking.
This concept was further explored by Burnstein and suggested that biomechanically body joints and motor control works together as functional unit and not as single limb movement.
Bobath and proprioceptive neuromuscular facilitation (PNF) concepts further explained that movements of the eye, head and neck facilitate trunk movements.
Electromyography studies have shown that both single and rhythmical jaw opening and closing movements not only produced well-coordinated jaw and head-neck movements but also produced atlanto-occipital and cervical spine joints movements.
The author further concluded that mouth opening and closing in fetal yawning is associated with head extension-flexion movements indicating that functional connections between the jaw and head-neck is innate.
A human jaw or masticatory system is connected to the motor system through cranial nerves unlike central motor system which is connected to the body through spinal motor system.
Brainstem central pattern generator (CPG) control masticatory system through descending pathways and are involved in voluntary movements of the jaw such as mouth opening and closing.
The higher brain centers cortical masticatory area and primary motor cortex control these movements.
In the current back pain literature core stability exercises have been used in the management of chronic low back pain.
The jaw is connected to the head-neck and neck is connected to the trunk.
Therefore there is to study the effects of core stability exercises performed with and without jaw movements in the management of chronic low back pain.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
A randomized experimental controlled trial will be carried out to compare the effectiveness of core stabilization exercises performed with and without jaw movements in the management of nonspecific chronic low back pain.
A total of 80 male and female volunteers having subjects with chronic nonspecific low back pain will be recruited in this study.
All subjects will be assessed for transverse abdominal muscle strength contraction, pain and disability using Pressure Biofeedback Unit (BPU), Numeric Pain Rating Scale (NPRS 0-10cm) and Ronald Morris Disability Questionnaire (RMDQ 0-24) respectively.
The scores on the mentioned scales will be documented as per guidelines.
After baseline assessment, all subjects will be allocated to two groups through computer-generated random sampling.
Group 1 will perform core stability exercises alone; Group 2 will perform core stability exercises with teeth clenching This study will be conducted at the Physiotherapy Department of Sindh Institute of Physical Medicine and Rehabilitation (SIPM&R).
The computer-generated random sampling technique will be used to allocate the participants into the study groups.
Data will be analyzed using SPSS 22 and one-way repeated measure ANOVA will be applied to see the mean difference in the 2 groups.
For pair-wise comparison, the Tukey test will be applied.
For pain and disability scales Friedman's test will be applied to see the two scales' median differences.
Study Type
Interventional
Enrollment (Actual)
80
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
SIndh
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Karachi, SIndh, Pakistan, 75400
- Sindh Institute of Physical Medicine & Rehabilitation
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 45 years (Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
· Participants having chronic low back pain lasting more than 12 weeks.
- Age 20-45 years
- Participants having nonspecific chronic low back pain with or without referred leg pain.
- Both male and female patients.
- Currently seeking care for low back pain.
- No known TMJ pathology.
- Had Magnetic Resonance Image (MRI) to exclude serious pathology and been diagnosed by the consultant and non-specific low back pain.
Exclusion Criteria:
· Participants with known or suspected serious spinal pathology (fracture, metastatic, inflammatory or infective diseases of the spine, cauda equine syndrome/widespread neurological disorder, lumbar spondylosis, stenosis, spondylolisthesis).
- Compromised nerve root
- Previous spinal surgery or scheduled for major surgery during the treatment.
- Co-morbid health conditions that would prevent active participation in the exercise programs such as asthma.
- Low back pain having less than 12 weeks history.
- Known Temporomandibular joint pathology or jaw pain.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: core stability exercises with teeth clenching
The intervention frequency will be 2 sessions per week for the duration of 6 weeks, comprising of 45 minutes session.
Both groups will receive heat pack on lumbar spine for 12 minutes and both interventions will be held under the supervision of qualified Musculoskeletal Physiotherapists.
During intervention and after 6 weeks of intervention, both groups will be given a home exercise program consist of same exercises they have carried out in the clinic for the duration another 6 weeks.
The participants will be asked to keep diaries of their exercises they have carried out each week.
|
The intervention frequency will be 2 sessions per week for the duration of 6 weeks, comprising of 45 minutes session.
Both groups will receive heat pack on lumbar spine for 12 minutes and both interventions will be held under the supervision of qualified Musculoskeletal Physiotherapists.
During intervention and after 6 weeks of intervention.
The intervention frequency will be 2 sessions per week for the duration of 6 weeks, comprising of 45 minutes session.
Both groups will receive heat pack on lumbar spine for 12 minutes and both interventions will be held under the supervision of qualified Musculoskeletal Physiotherapists.
During intervention and after 6 weeks of intervention.
|
Active Comparator: core stability exercises alone
The intervention frequency will be 2 sessions per week for the duration of 6 weeks, comprising of 45 minutes session.
Both groups will receive heat pack on lumbar spine for 12 minutes and both interventions will be held under the supervision of qualified Musculoskeletal Physiotherapists.
During intervention and after 6 weeks of intervention, both groups will be given a home exercise program consist of same exercises they have carried out in the clinic for the duration another 6 weeks.
The participants will be asked to keep diaries of their exercises they have carried out each week.
|
The intervention frequency will be 2 sessions per week for the duration of 6 weeks, comprising of 45 minutes session.
Both groups will receive heat pack on lumbar spine for 12 minutes and both interventions will be held under the supervision of qualified Musculoskeletal Physiotherapists.
During intervention and after 6 weeks of intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Numeric Pain Rating Scale
Time Frame: At baseline
|
The Numeric Pain Rating Scale (NPRS) is a unidimensional measure of pain intensity in adults, including those with chronic pain due to rheumatic diseases.
|
At baseline
|
Numeric Pain Rating Scale
Time Frame: At 6th weeks
|
The Numeric Pain Rating Scale (NPRS) is a unidimensional measure of pain intensity in adults, including those with chronic pain due to rheumatic diseases.
|
At 6th weeks
|
Numeric Pain Rating Scale
Time Frame: At 12th weeks
|
The Numeric Pain Rating Scale (NPRS) is a unidimensional measure of pain intensity in adults, including those with chronic pain due to rheumatic diseases.
|
At 12th weeks
|
Roland Morris Questionnaire (RMQ):
Time Frame: At baseline
|
RMQ is a standardized subjective assessment questionnaire that is used as Outcome tool to assess functional disability in acute and sub-acute low back pain.
|
At baseline
|
Roland Morris Questionnaire (RMQ):
Time Frame: At 6th weeks
|
RMQ is a standardized subjective assessment questionnaire that is used as Outcome tool to assess functional disability in acute and sub-acute low back pain.
|
At 6th weeks
|
Roland Morris Questionnaire (RMQ):
Time Frame: At 12th weeks
|
RMQ is a standardized subjective assessment questionnaire that is used as Outcome tool to assess functional disability in acute and sub-acute low back pain.
|
At 12th weeks
|
Pressure Biofeedback unit (PBU):
Time Frame: At baseline
|
Pressure Biofeedback unit (PBU) PBU is a reliable and valid tool for recording core stability muscle strength .
|
At baseline
|
Pressure Biofeedback unit (PBU):
Time Frame: A 6th weeks
|
Pressure Biofeedback unit (PBU) PBU is a reliable and valid tool for recording core stability muscle strength .
|
A 6th weeks
|
Pressure Biofeedback unit (PBU):
Time Frame: At 12th weeks
|
Pressure Biofeedback unit (PBU) PBU is a reliable and valid tool for recording core stability muscle strength .
|
At 12th weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Muhammad Khan, MSAPT, University of Lahore
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Tsao H, Druitt TR, Schollum TM, Hodges PW. Motor training of the lumbar paraspinal muscles induces immediate changes in motor coordination in patients with recurrent low back pain. J Pain. 2010 Nov;11(11):1120-8. doi: 10.1016/j.jpain.2010.02.004.
- Sung PS. Disability and back muscle fatigability changes following two therapeutic exercise interventions in participants with recurrent low back pain. Med Sci Monit. 2013 Jan 14;19:40-8. doi: 10.12659/msm.883735.
- Raine S, Meadows L, Lynch-Ellerington M. Bobath Concept: Theory and Clinical Practice in Neurological Rehabilitation. Wiley-Blackwell. 2009. 4- Bernstein, N. The Coordination and Regulation of Movement. Pergamon Press, Oxford. Bishop, B. 1967.
- Adler SS, Beckers D, Buck M. PNF in Practice: An Illustrated Guide. New York, NY: Springer. 2007.
- Voss DE, Ionta MK, Myers BJ. Proprioceptive Neuromuscular Facilitation. Patterns and Techniques. Philadelphia, PA: Harper & Row Publishers. 1985.
- HUMPHREY T. The spinal tract of the trigeminal nerve in human embryos between 7 1/2 and 8 1/2 weeks of menstrual age and its relation to early fetal behavior. J Comp Neurol. 1952 May;97(1):143-209. doi: 10.1002/cne.900970109. No abstract available.
- Zafar H, Eriksson PO, Nordh E, Haggman-Henrikson B. Wireless optoelectronic recordings of mandibular and associated head-neck movements in man: a methodological study. J Oral Rehabil. 2000 Mar;27(3):227-38. doi: 10.1046/j.1365-2842.2000.00505.x.
- Zafar H, Nordh E, Eriksson PO. Temporal coordination between mandibular and head-neck movements during jaw opening-closing tasks in man. Arch Oral Biol. 2000 Aug;45(8):675-82. doi: 10.1016/s0003-9969(00)00032-7.
- Barry J. Sessle ,LimorAvivi-Arber, and Gregory M. Murray. Motor Control of Masticatory Muscles. Craniofacial Muscles: A New Framework for Understanding the Effector Side of Craniofacial Muscle Control. L.K. McLoon and F.H. Andrade (eds.) Toronto. 2013.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 1, 2021
Primary Completion (Actual)
April 30, 2023
Study Completion (Actual)
April 30, 2023
Study Registration Dates
First Submitted
February 3, 2021
First Submitted That Met QC Criteria
March 13, 2021
First Posted (Actual)
March 16, 2021
Study Record Updates
Last Update Posted (Estimate)
May 4, 2023
Last Update Submitted That Met QC Criteria
May 3, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 00001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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