Efficacy Of Non-Invasive High Power Laser Acupuncture Stimulation In Chronic Non-Specific Low Back Pain

Sponsor
Cairo University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05970419
Collaborator
(none)
60
1
2
3.7
16.3

Study Details

Study Description

Brief Summary

This study will be conducted to answer the following question: Does high power laser acupuncture has any effect on pain, back range of motion, function, quality of life, fatigue and level of satisfaction in chronic nonspecific low back pain patients?

Condition or Disease Intervention/Treatment Phase
  • Other: high power laser acupuncture (HPLA)
  • Other: conventional treatment
  • Other: Sham laser
N/A

Detailed Description

The aims of this study are:
  1. To investigate the effect of high power laser acupuncture on pain in chronic nonspecific low back pain patients

  2. To investigate the effect of high power laser acupuncture on back range of motion (flexion, extension, side bending and rotation) in chronic nonspecific low back pain patients.

  3. To investigate the effect of high power laser acupuncture on function in chronic nonspecific low back pain patients.

  4. To investigate the effect of high power laser acupuncture on quality of life in chronic nonspecific low back pain patients.

  5. To investigate the effect of high power laser acupuncture on back muscle fatigue in chronic nonspecific low back pain patients.

  6. To investigate the effect of high power laser acupuncture on level of satisfaction in chronic nonspecific low back pain patients.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Efficacy Of Non-Invasive High Power Laser Acupuncture Stimulation In Chronic Non-Specific Low Back Pain
Anticipated Study Start Date :
Aug 10, 2023
Anticipated Primary Completion Date :
Oct 30, 2023
Anticipated Study Completion Date :
Nov 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: High power laser acupuncture group

This group will receive high power laser acupuncture (HPLA) +conventional therapy

Other: high power laser acupuncture (HPLA)
HPLA will be provided in Wave length 1064 (nm) Energy Density (0.510-0.1780 J/cm 2) Power Average (3000 W) pulsed Time per Point (14s) for acupoints. Although a maximum power of 8000 W was reported in two studies, the average power of the lasers used in t

Other: conventional treatment
Superficial heat (hot packs). Will be applied 10 - 15 minutes. Guideline-endorsed treatment is to stay active, return to normal activity, and to exercise. Different exercise types are used in the treatment of CLBP such as strength and aerobic training on land as well as specific exercises such as motor control exercises (MCE). General exercises activating the extensor (paraspinals) and flexor (abdominals) muscle groups will be used.

Active Comparator: Conventional treatment group

This group will receive sham laser and The first line of chronic nonspecific low back pain treatment is the conventional treatment.

Other: conventional treatment
Superficial heat (hot packs). Will be applied 10 - 15 minutes. Guideline-endorsed treatment is to stay active, return to normal activity, and to exercise. Different exercise types are used in the treatment of CLBP such as strength and aerobic training on land as well as specific exercises such as motor control exercises (MCE). General exercises activating the extensor (paraspinals) and flexor (abdominals) muscle groups will be used.

Other: Sham laser
sham laser (Not active)

Outcome Measures

Primary Outcome Measures

  1. Assessing the change in intensity of pain [at baseline and after 4 weeks of intervention]

    By using visual analoge scale (VAS). It is a valid and reliable measure to assess pain intensity level by patients by making a mark determining a decimal number from 0 to 100 (mm) on line with 'no pain' to the left and severe pain could be to the right. The subjects will rate their perception of pain by making a mark on the VAS line. The distance from the left to the mark will be measured and the accuracy will be adjusted to one decimal place.

  2. Assessing the change in Back Range of Motion [at baseline and after 4 weeks of intervention]

    By using the Back Range of Motion Instrument (BROM). It is a valid and reliable measure to assess back range of motion (flexion, extension, side bending and rotation) The BROM is uses a patented inclinometer based instrument for measuring lateral side bend in the preferred upright position. The magnetic inclinometer and reference eliminate hip substitution errors. The BROM Basic includes two Universal Inclinometers for measuring flexion and extension of the lumbar spine.

  3. Assessing the change in Quality of Life [at baseline and after 4 weeks of intervention]

    By using the short version of the WHO Quality of Life Instrument in Arabic. It will be used to assess quality of life. The World Health Organization Quality-of-Life Scale (WHOQOL-BREF) provides a reliable, valid, and brief assessment of quality-of-life. There will be a four-domain score. The four domain scores will denote an individual perception of quality of life in each particular domain. Domains scores are scaled in a positive direction higher score denote higher quality of life. The mean score of items within each domain is used to calculate the domain score. Mean scores are then multiplied by 4 in order to make domain scores comparable with the scores used in the WHOQOL-100.

  4. Assessing the change in endurance of the trunk extensor muscles [at baseline and after 4 weeks of intervention]

    By using Biering-Sorensen test. The Sorensen test allows for a rapid, simple, and reproducible evaluation of the isometric endurance of the trunk extensor muscles. It discriminates between healthy individuals and patients with low back pain and may predict the occurrence of low back pain in the near future. The test consists in measuring the amount of time a person can hold the unsupported upper body in a horizontal prone position with the lower body fixed to the examining table. The Biering-Sørensen test for measuring back muscle fatigue is valid and provides reliable measures of position-holding time and can discriminate between subjects with and without nonspecific low back pain.

  5. Assessing the change in patient satisfaction [at baseline and after 4 weeks of intervention]

    By using The MedRisk Instrument for Measuring Patient Satisfaction (MRPS). A Self-report measures that sample a variety of items provide clinicians with an array of information that may assist in assessing patient satisfaction. The MRPS questionnaire is valid and reliable for measuring patient satisfaction. It has a 2-factor structure: "internal," relating to the patient-therapist interaction, and "external," describing no therapist issues such as admissions and clinic environment.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
Subjects will be included in this study will be having all of the following criteria:
  1. Age over 18 years of age.

  2. Both genders (males and females).

  3. Normal BMI ranges between 18.5:24.9 kg/m2.

  4. 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.

  1. CNSLBP patients will be diagnosed based on the standard criteria, including pain and tenderness on lower back and a negative result for all special tests for lumber neurological examination.
Exclusion Criteria:
  1. History of any surgical procedure in the back or the lower extremities.

  2. Back pain secondary to known specific pathology (e.g. infection, tumor, osteoporosis, fracture, structural deformity, inflammatory disorder (e.g. ankylosing spondylitis) or cauda equine syndrome).

  3. Patient with lumbar instability including spondylolisthesis.

  4. Red flags (e.g. fever, unexplained weight loss, progressive weakness, radiation to lower limb, bowel and bladder dysfunction).

  5. Pregnancy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Outpatient clinic faculty of physical therapy cairo university Dokki Egypt

Sponsors and Collaborators

  • Cairo University

Investigators

  • Principal Investigator: Tasnim Mohamed, Cairo University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Tasnim Mohamed Elfeky, Principal Investigator, Cairo University
ClinicalTrials.gov Identifier:
NCT05970419
Other Study ID Numbers:
  • Tasnim Mohamed Elfeky
First Posted:
Aug 1, 2023
Last Update Posted:
Aug 1, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 1, 2023