- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06612918
Effect of High-intensity Laser Acupuncture on Muscle Performance, Pain and Quality of Life in Low Back Pain
Effect of High-Intensity Laser Acupuncture on Muscle Performance, Pain, and Quality of Life in Patients With Chronic Nonspecific Low Back Pain: A Randomized Controlled Trial
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Giza, Egypt, 11251
- Egypt
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- The patients had CNSLBP with age from 20 to 40 years from both genders.
- Patients will be referred from an orthopedist with diagnosis of chronic low back pain without underlying pathological causes.
- The patients with chronic nonspecific low back pain more than 3months. Minimum pain intensity of 30 mm on the visual analogue scale (VAS) for pain, which ranges from 0 to 100 mm.
- Patients with normal BMI ranges between 18.5:24.9 kg/m2.
- The study populations must be willing to participate in the study
Exclusion Criteria:
- Neurological, infectious diseases and systemic illness such as rheumatologic diseases,systemic lupus erythematosus, diabetes mellitus type I or II.
- Psychiatric/mental deficit.
- Patients who had a previous surgical history (within 6 months) will also excluded.
- participation in other treatment within the previous 3 month.
- Pregnancy.
- History of spinal fracture, tumor, osteoporosis
- use of medication, such as corticosteroids, anticonvulsants, and antiinflammatory drugs that may affect the outcome of the study.
- prior history of adverse effects to physical stimulation therapy.
- significant physical or mental deficiencies preventing a clear understanding of the study procedure.
- spinal stenosis, thyroid dysfunctions, obesity, pace-maker.
Study Plan
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 |
|---|---|
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Experimental: high-intensity laser acupuncture and the exercise program
The patients will receive high-intensity laser acupuncture and the exercise program three times a week for four weeks.
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The experimental group will receive high-intensity lasers, and the treatment will be performed at 15 acupuncture points: unilateral GV3, GV4, and GV5, and bilateral BL 20, BL23, BL24, BL25, BL40, and GB30.
Exercises program: The patients will perform this exercise program in the form of: strengthening exercises for abdominal and back muscles; lumbar stabilization exercises; and stretching exercises.
Other Names:
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Sham Comparator: sham laser acupuncture and exercises program.
The patients will receive sham acupuncture laser and the exercise program three times a week for four weeks.
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The patients will receive a sham laser acupuncture and the exercise program in the form of: strengthening exercises for abdominal and back muscles; lumbar stabilization exercises and stretching exercises.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
muscle performance
Time Frame: up to four weeks]
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Isokinetic dynamometer will be used for measuring muscle performance of back extensors and flexors
|
up to four weeks]
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muscle performance
Time Frame: follow up after 1 month
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Isokinetic dynamometer will be used for measuring muscle performance of back extensors and flexors
|
follow up after 1 month
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Intensity
Time Frame: up to four weeks
|
Visual Analogue Scale (VAS) will be used by the patient to mark his/her level of pain between 0 to100 milliliters line. Zero usually represents 'no pain at all' whereas the upper limit represents 'the worst pain ever possible'. |
up to four weeks
|
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Pain Intensity
Time Frame: follow up after 1 month
|
Visual Analogue Scale (VAS) will be used by the patient to mark his/her level of pain between 0 to100 milliliters line. Zero usually represents 'no pain at all' whereas the upper limit represents 'the worst pain ever possible'. |
follow up after 1 month
|
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Quality of Life (WHOQOL-BREF)
Time Frame: up to four weeks
|
The World Health Organization Quality-of-Life Scale (WHOQOL-BREF) will be used in assessment of quality-of-life.The Arabic translation of the WHOQOL-BREF has impressive reliability and validity indices.
There will be four domains.
The four domain scores will denote an individual perception of quality of life in each particular domain.Domain scores are scaled in a positive direction higher scores denote higher quality of life.
|
up to four weeks
|
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Quality of Life (WHOQOL-BREF)
Time Frame: follow up after 1 month
|
The World Health Organization Quality-of-Life Scale (WHOQOL-BREF) will be used in assessment of quality-of-life.The Arabic translation of the WHOQOL-BREF has impressive reliability and validity indices.
There will be four domains.
The four domain scores will denote an individual perception of quality of life in each particular domain.Domain scores are scaled in a positive direction higher scores denote higher quality of life.
|
follow up after 1 month
|
Collaborators and Investigators
Sponsor
Collaborators
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 (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
- P.T.REC/012/005224
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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