Actively Recruiting

Phase Not Applicable
Age: 25Years - 45Years
All Genders
ID06796881

Instrument Assisted Soft Tissue Mobilization Versus Myofascial Release in Patients With Chronic Non-Specific Low Back Pain

Led by Cairo University · Updated on 2025-01-28

66

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of two types of soft tissue treatments, instrumental-assisted soft tissue mobilization and myofascial release, on people with chronic nonspecific low back pain. This condition affects many workers and limits daily and work activities, and current treatments often do not provide satisfactory relief. The study aims to compare these treatments by measuring pain intensity, pressure pain threshold, back function, and range of motion. Participants are divided into three groups: one group receives instrumental-assisted soft tissue mobilization along with exercises, another group receives myofascial release with exercises, and a control group receives exercises only. The instrumental-assisted mobilization uses a special tool applied for 40-120 seconds followed by a 5-minute ice pack. The myofascial release involves a therapist applying specific pressure techniques for 5 minutes on each side of the lower back. All groups participate in a 6-week exercise program including several strengthening exercises. During the study, participants will be assessed at the start and after 6 weeks for changes in pain using a visual analogue scale, pressure pain threshold with an algometer, lumbar spine range of motion in multiple directions using a device, and back function with a disability index questionnaire. The study is randomized and single-blind with 66 patients aged 25 to 45. The lead sponsor is Cairo University, and monitoring will focus on these outcomes to better understand treatment effects on chronic low back pain.

CONDITIONS

Brief Title

Instrument Assisted Soft Tissue Mobilization Versus Myofascial Release in Patients With Chronic Non¬Specific Low Back Pain

Who Can Participate

Age: 25Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with chronic non-specific low back pain for more than 3 months
  • Age between 25 and 45 years
Not Eligible

You will not qualify if you...

  • Serious spinal pathologies such as fractures, tumors, or inflammatory diseases (e.g., ankylosing spondylitis)
  • Nerve root compromise, disk herniation, spondylolisthesis with neurological involvement, or spinal canal narrowing
  • Pregnant women
  • Cancer patients
  • Lower limb injuries
  • Body mass index (BMI) greater than 25

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 weeks

Participants receive either instrument assisted soft tissue mobilization with exercises, myofascial release with exercises, or exercises only over a 6-week period to manage chronic non-specific low back pain.

12 treatment sessions over 6 weeks

Trial Site Locations

Total: 1 location

1

the Outpatient Clinic of the Police Authority Hospital

Cairo, Egypt

Actively Recruiting

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Research Team

D

Dalia salah Ahmed Elshatoury, physical therapist

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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