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CompletedNCT07196709Updated Jul 9, 2026

Effect of High-power Laser Acupuncture on Fatigue and Proprioception in Low Back Pain

An interventional study of high-power laser acupuncture and the exercise program and sham laser acupuncture and the exercises program in Chronic Nonspecific Low-back Pain, sponsored by Cairo University. Completed at 1 site in Egypt. Open to participants aged 20 Years to 40 Years. Per ClinicalTrials.gov, last updated 2026-07-09.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
20 Years to 40 Years
Sex
All
01

Study summary

To investigate the effect of high-intensity laser acupuncture on fatigue, proprioception, back pain and Pain self-efficacy in patients with chronic nonspecific low back pain (CNLBP).

Read the detailed description

Chronic non-specific low back pain (CNSLBP) is a persistent back pain that affects people of all ages and significantly impacts individuals' functional activities. Fatigue and impaired proprioception are common complaints associated with CNSLBP, contributing to diminished physical performance and exacerbation of symptoms. While various treatment modalities exist, there is ongoing interest in exploring novel approaches to manage this condition effectively.Laser photobiomodulation (PBM) therapy is a noninvasive that stimulates cells, pain receptors, and the immune system and can cause analgesic effects. Recently, high-power lasers have been used for managing musculoskeletal dysfunction that allows for more energy deposition in deep tissues, resulting in both biological and thermal effects. High-power laser acupuncture (HPLA) has emerged as a promising intervention that combines the therapeutic effects of high-power laser therapy and the principles of acupuncture point stimulation on the body (acupoints) to induce physiological effect. However, there is limited evidence supporting this combined approach. For that, this study aims to investigate the effect of HPLA on fatigue, proprioception back pain and Pain self-efficacy in patients with CNSLBP. With this current randomized controlled trial, we seek to provide evidence-based insights into the potential effects of this combined approach on measurements of fatigue, proprioception, back pain and Pain self-efficacy.

02

Conditions studied

  • Chronic Nonspecific Low-back Pain

Keywords

  • low back pain
  • high-power laser acupuncture
  • fatigue
  • proprioception
  • Pain self-efficacy
03

In context

Low Back Pain

2,818 studies on the registry are indexed under Low Back Pain; 482 are open to participants now.

This study's enrollment of 60 is close to the median of 60 across 2,268 interventional studies indexed under Low Back Pain.

Browse Low Back Pain studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 1. The patients had CNSLBP with age from 20 to 40 years from both genders.

    2. Patients diagnosis with chronic low back pain without underlying pathological causes.

    3. 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.

    4. Patients with BMI ranges between 18.5:29.9 kg/m2.

    5. The study populations must be willing to participate in the study

Exclusion criteria

Exclusion Criteria:

  1. Neurological, infectious diseases and systemic illness such as rheumatologic diseases,systemic lupus erythematosus, diabetes mellitus type I or II.
  2. Psychiatric/mental deficit.
  3. Patients who had a previous surgical history (within 6 months) will also excluded
  4. participation in other treatment within the previous 3 month.
  5. Pregnancy.
  6. History of spinal fracture, tumor, osteoporosis
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    high-power laser acupuncture and the exercise program

    The patients will receive high-power laser acupuncture and the exercise program three times a week for 4 weeks.

    Device: high-power laser acupuncture and the exercise program

  • 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.

    Device: sham laser acupuncture and the exercises program

Interventions

  • Devicehigh-power laser acupuncture and the exercise program

    The experimental group will receive high-power 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

    Also known as: high-intensity laser acupuncture

  • Devicesham laser acupuncture and the exercises program

    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.

    Also known as: sham laser acupuncture

06

What researchers measure

Primary outcomes

  1. fatigue

    Isokinetic dynamometer will be used for measuring fatigue of back muscles.

    Time frame: up to six weeks

  2. fatigue

    The Biering-Sørensen test will be used for measuring fatigue of back muscles

    Time frame: up to six weeks

  3. proprioception

    Isokinetic dynamometer will be used for assessing lumber proprioception

    Time frame: up to six weeks

Secondary outcomes

  1. Pain Intensity

    The Visual Analogue Scale (VAS) will be used by the patient to mark his/her level of pain on a 0 to 100 millimeter line. Zero usually represents 'no pain at all,' whereas the upper limit represents 'the worst pain ever possible.' Higher scores represent worse pain intensity, and lower scores represent less pain.

    Time frame: up to six weeks

  2. Pain-Related Self-Efficacy

    The Arabic version of the Pain Self-Efficacy Questionnaire (PSEQ-A) will be used to assess patients ' confidence in managing pain and performing daily activities. Higher scores reflect greater self-efficacy, indicating stronger confidence in coping with pain.

    Time frame: up to six weeks

07

Study locations

1 site
  • Doaa Ayoub Elimy
    Giza, 11251, Egypt
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07196709
Lead sponsor
Cairo University
Responsible party
Doaa Ayoub Elimy Mohammed (Lecturer of physical therapy for basic science department., faculty of physical Therapy, Cairo University) — Principal investigator
First posted
Sep 29, 2025
Start date
Nov 30, 2025
Primary completion
Jun 30, 2026
Completion
Jun 30, 2026
Last update
Jul 9, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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