Effect of Acupuncture Dry Needle in Treatment of Chronic Mechanical Low Back Pain

Sponsor
Prince Sattam Bin Abdulaziz University (Other)
Overall Status
Completed
CT.gov ID
NCT06140264
Collaborator
(none)
30
1
2
5.7
5.3

Study Details

Study Description

Brief Summary

Low back pain affects about 60% to 90% of the working-age population in modern industrial society. Chronic mechanical low back pain (CMLBP) is the most common problem of the working-age population in modern industrial society; it causes a substantial economic burden due to the wide use of medical services and absence from work. The purpose of this trial was to evaluate the short-term effect of acupuncture dry needle in treatment of chronic mechanical low back pain.

Condition or Disease Intervention/Treatment Phase
  • Other: Acupuncture dry needle
N/A

Detailed Description

Low back pain affects about 60% to 90% of the working-age population in modern industrial society. Chronic mechanical low back pain (CMLBP) is the most common problem of the working-age population in modern industrial society; it causes a substantial economic burden due to the wide use of medical services and absence from work. The purpose of this trial was to evaluate the short-term effect of acupuncture dry needle in treatment of chronic mechanical low back pain. Thirty patients their age ranged from 18 - 43 years participated in our study and divided randomly into two equal groups suffering from nonspecific low back pain. The first group (A) consist of 15 patients receiving acupuncture dry needle over trigger points of back muscles followed by stretching and strengthening exercises for back muscles, the second group (B) consist of 15 patients receiving only stretching and strengthening exercises for back muscles. The following parameters including pain severity, functional disability and lumbar range of motion (flexion, extension, right side bending and left side bending) were measured before and after treatment.

Study Design

Study Type:
Interventional
Actual Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Short Term Effect of Acupuncture Dry Needle in Treatment of Chronic Mechanical Low Back Pain: A Randomized Controlled Clinical Trial
Actual Study Start Date :
Sep 1, 2022
Actual Primary Completion Date :
Jan 11, 2023
Actual Study Completion Date :
Feb 21, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Acupuncture dry needle

This group received acupuncture dry needle over trigger points of back muscles followed by stretching and strengthening exercises for back muscles, 2 sessions per week for 2 weeks.

Other: Acupuncture dry needle
The muscles that have been treated iliocostalis lumborum, quadratus lumborum, gluteus medius and piriformis muscles. The patients received 2 sessions per week for 2 weeks.

No Intervention: Stretching and strengthening exercises

This group received only stretching and strengthening exercises for back muscles.

Outcome Measures

Primary Outcome Measures

  1. Pain intensity [Four weeks]

    Pain was assessed by Visual Analog Scale (VAS). VAS is a scale that allows continuous data analysis and uses a 10 cm line with 0 in one end (no pain) and 10 (worst pain) on the other end. Patients were asked to place a mark along the line to denote their level of pain.

Secondary Outcome Measures

  1. Functional disability [Four weeks]

    Functional disability of each patient was assessed by Oswestery disability questionnaire. It is valid and reliable tool. It is consists of 10 multiple choice questions for back pain, patient select one sentence out of six that best describe his pain, Higher scores indicated great pain. Scores (0-20%) minimal disability, Scores (20%- 40%) moderate, Scores (40% - 60%) severe, Scores (60%-80%) crippled, Scores (80% - 100%) patients are confined to bed.

  2. Lumbar range of motion [Four weeks]

    Modified-modified Schober flexion technique was used based on the work of Williams et al17 this method is reliable and valid in measuring range of motion of lumbar flexion. The investigator stood behind the standing patient to identify the posterior superior iliac spines with her or his thumbs, and then an ink mark was drawn along the midline of the lumbar spine horizontal to the posterior superior iliac spines. Another ink mark was made 15 cm above the original mark; the distance between superior and inferior skin marks was measured. Then the investigator instructed the patient to bend forward into full lumbar flexion and the new distance between superior and inferior skin marks was measured.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 43 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age ranges from 18 to 43 years old14.

  2. Pain of at least 30 mm to 70 mm on a visual analogue scale (VAS) from 0 mm (no pain) to 100 mm (worst imaginable pain).

  3. Presence of MTrPs at least in 4 muscles on any side.

  4. Patients had lower back myofascial pain syndrome for at least 3 months ago.

Exclusion Criteria:

A history of previous back surgery, neurologic deficit, current lower extremity symptoms, cardiopulmonary disease with decreased activity tolerance, rheumatologic conditions, polyarticular osteoarthritis, rheumatoid arthritis and advanced lumbar degenerative disease, patients receiving other treatment in the form of physical therapy or medication for the duration of the study that may interfere with the results of this study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Walid Kamal Abdelbasset Al-Kharj Riyadh Saudi Arabia 11942

Sponsors and Collaborators

  • Prince Sattam Bin Abdulaziz University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Prince Sattam Bin Abdulaziz University
ClinicalTrials.gov Identifier:
NCT06140264
Other Study ID Numbers:
  • RHPT/022/035
First Posted:
Nov 18, 2023
Last Update Posted:
Nov 18, 2023
Last Verified:
Nov 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Prince Sattam Bin Abdulaziz University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 18, 2023