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High Intensity Laser vs Instrument-assisted Soft Tissue Mobilization on Trapezius Myofascial Pain Syndrome

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

High Intensity Laser
Myofascial Pain Syndrome
Instrument Assisted Soft Tissue Mobilization
Trapezius Muscle Strain

Treatments

Device: High Intensity Laser
Other: Conventional treatment
Other: Instrument-assisted Soft Tissue Mobilization

Study type

Interventional

Funder types

Other

Identifiers

NCT06990932
Ahmed-005701

Details and patient eligibility

About

The purpose of the study was to

  1. Investigate the effect of high-intensity laser therapy versus Instrument-assisted soft tissue mobilization on pain level in patients with myofascial pain syndrome of upper trapezius muscle.
  2. Investigate the effect of High intensity laser therapy versus Instrument-assisted soft tissue mobilization on ROM in patients with myofascial pain syndrome of upper trapezius muscle

Full description

Myofascial pain syndrome is a common musculoskeletal pain affecting 30% of patients in primary care. It is characterized by trigger points in the upper trapezius muscle, which is linked to neck and shoulder pain. Non-invasive treatments like exercises, manipulation, and physical agents have been suggested for managing neck pain. Laser therapy, including low-level and high-intensity, has been found effective in reducing pain intensity and improving functional activity. Instrument-assisted soft tissue mobilization is another technique used to treat Myofascial pain syndrome. Instrument-assisted soft tissue mobilization stimulates connective tissue remodeling, resorbing excessive fibrosis, and promoting collagen repair and regeneration. The study aims to investigate the effect of high intensity laser therapy versus Instrument-assisted soft tissue mobilization in treating Myofascial pain syndrome of the upper trapezius muscle.

Enrollment

60 patients

Sex

All

Ages

20 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. The patient age ranged from 20 to 50 years
  2. Presence of myofascial trigger points in the upper trapezius muscle
  3. Having neck discomfort symptoms that were triggered by certain neck positions and by palpating the cervical musculature for at least three months
  4. Patient willing and able to participate in an exercise program safely

Exclusion criteria

  1. medical red flag history (such as tumour, fracture, metabolic diseases, rheumatoid arthritis and osteoporosis)
  2. Neck pain with cervical radiculopathy or neck pain associated with externalized cervical disc herniation.
  3. If the patient had previous surgery in the neck area (irrespective of the reason for the operation)
  4. Neck pain accompanied by vertigo caused by vertebra basilar insufficiency or accompanied by non-cervicogenic headaches

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 3 patient groups

High Intensity Laser
Experimental group
Description:
this group consists of 20 subjects will receive conventional treatment combined with High-intensity laser therapy, three times per week for one month
Treatment:
Other: Conventional treatment
Device: High Intensity Laser
Instrument-assisted soft tissue mobilization
Active Comparator group
Description:
this group consists of 20 subjects will receive conventional treatment combined with Instrument-assisted soft tissue mobilization, three times per week for one month
Treatment:
Other: Instrument-assisted Soft Tissue Mobilization
Other: Conventional treatment
conventional treatment
Active Comparator group
Description:
this group consists of 20 subjects will receive conventional treatment only, three times per week for one month
Treatment:
Other: Conventional treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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