Low Back Pain Clinical Trial
Official title:
Effects of Bilateral Asymmetrical Limbs Proprioceptive Neuromuscular Facilitation on Multifidus Muscle in Chronic Low Back Pain (CLBP)
Verified date | February 2021 |
Source | University of Karachi |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The low back pain is a leading cause to limit individual functional activities worldwide and 60%-80% of adults are probable to get low back pain at least once in life time. Whereas, the chronic low back pain prevalence is 10%.The current literature suggests that any exercise is beneficial for reducing chronic nonspecific low back pain. This limits evidence regarding superiority of specific exercise for low back pain treatment. Therefore, a randomized control trial will be conducted at department of physiotherapy to assess which treatment is more effective in chronic low back pain at department of physiotherapy, institute of physical medicine and rehabilitation, Dow University of Health Sciences after synopsis approval. Overall 150 participants with 18-40 years old having chronic low back pain will be eligible and they will be included through non-probability, purposive sampling technique. The written informed consent will be taken from all the participants. They will be divided through systematic random sampling method into two groups, 75 in each group. Group A (experimental group) will receive Bilateral, asymmetrical limbs PNF pattern exercises and group B (control group) will receive Swiss ball exercises. All participants will be assessed using assessment form. Pain and functional disability will be measured by subjective outcome tools, visual analogue scale with 0-10cm and Oswestry disability index , respectively. Range of movement of lumbar and multifidus muscle activity will be measured by objective outcome tool, modified-modified Schober's test and surface electromyography, respectively. The pre & post treatment outcomes will be collected and recorded. Treatment sessions will be given thrice a week for 5 weeks. A maximum drop-out rate of 20% is expected. The Mean ± SD will be calculated for quantitative variables and frequencies and percentages for qualitative variables. The recorded outcome variables before and after the five weeks of treatment will be compared and analysed. The p-value of 0.05 will be considered as level of significant.
Status | Completed |
Enrollment | 150 |
Est. completion date | January 17, 2021 |
Est. primary completion date | December 15, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 40 Years |
Eligibility | Inclusion Criteria: - Chronic Low back pain (pain for > 3 month) Exclusion Criteria: - Any history related to spinal surgery - Previous administration of epidural injections. - Low Back Pain due to specific pathology, - Neurological deficits (like stroke) - Clinical disorder contraindicated to exercise. |
Country | Name | City | State |
---|---|---|---|
Pakistan | Aftab Ahmed Mirza Baig | Karachi | Sindh |
Lead Sponsor | Collaborator |
---|---|
University of Karachi |
Pakistan,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual analogue scale | The visual analogue scale is used for measurement of pain intensity. It is a continuous scale. It comprises a horizontal or vertical 10 centimeters or 100 millimeters line. The participant is asked to indicate a point of pain intensity by placing a line perpendicular to the Visual analogue scale line. The scale is most commonly referred by "no pain" with score of 0 and "worst imaginable pain" with score of 100 on the scale. The higher scores shows higher pain intensity and lower scores shows lower pain intensity. | Change from baseline pain intensity at 5 weeks. | |
Primary | Modified Modified Schober's test. | It is used during physical examination to assess the lumbar range of movement. It is highly co-related with lumbar range of movement measured through radiograph. | Change from baseline lumbar range of movement at 5 weeks. | |
Primary | Surface electromyography | It is a record of the electrical activity associated with muscular contraction. The electromyography is recorded and the peak amplitude [maximal voluntary isometric contraction] is selected manually and recorded. | Change from baseline multifidus muscle activity at 5 weeks | |
Secondary | Oswestry Disability Index | It is a standard questionnaire with questions regarding pain and the disabling effect on daily activities. Its score ranges from 0 to 100 (no disability to maximum disability). Cut off value score "9" shows sensitivity 62% and specificity 55%. | Change from baseline functional disability at 5 weeks |
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