Actively Recruiting

Phase Not Applicable
Age: 30Years - 60Years
All Genders
Healthy Volunteers
ID07293676

The Effects of Instrument-Assisted Soft Tissue Mobilization and Vibration Therapy on Pain, Functionality, and Kinesiophobia in Individuals With Lumbar Disc Herniation

Led by Istanbul Medipol University Hospital · Updated on 2026-03-27

45

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of Instrument-Assisted Soft Tissue Mobilization (IASTM) and vibration massage therapy on pain, physical function, and fear of movement (kinesiophobia) in adults with lumbar disc herniation. The study compares these therapies to conventional exercise to understand their impact on these symptoms in individuals diagnosed with disc herniation at the protrusion level who have experienced pain for at least three months. Participants will be randomly assigned to one of three groups: a conventional home exercise program, IASTM treatment, or percussion (vibration) massage therapy. The exercise group will perform stretching and strengthening exercises twice daily for four weeks with weekly phone follow-ups. The IASTM group will receive twice-weekly sessions using specialized stainless-steel tools applied to specific lower back muscles over six minutes per session. The vibration massage group will receive twice-weekly 10-minute sessions using a Theragun device targeting muscles in the lower back. During the study, participants will be assessed at the start and after four weeks of treatment using tools measuring pain levels (Visual Analog Scale), disability (Oswestry Disability Index), and fear of movement (Tampa Scale of Kinesiophobia). Researchers will monitor participants' adherence to exercise, collect feedback on symptoms, and observe changes in functionality and pain. The total study duration per participant covers the four-week treatment period, with safety and results monitored by Istanbul Medipol University Hospital.

CONDITIONS

Brief Title

IASTM and Vibration Effects on Pain, Functionality, and Kinesiophobia in Lumbar Disc Herniation

Who Can Participate

Age: 30Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals between 30 and 60 years of age
  • Diagnosed with lumbar disc herniation at the protrusion level
  • No cognitive, intellectual, or mental impairments and able to express themselves
  • Pain level greater than 5 on the Visual Analog Scale
  • Experiencing pain for at least 3 months
Not Eligible

You will not qualify if you...

  • History of lumbar surgery
  • Pregnancy
  • Spinal tumor or any other malignancy within the past six months
  • Received physiotherapy for low back pain within the last six months
  • Orthopedic conditions such as fractures
  • Neurological, rheumatological, or psychological disorders
  • Diagnosed with infection, spondylosis, spondylolysis, osteoporosis, or ankylosing spondylitis

AI-Screening

AI-Powered 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 - 4 weeks

Participants receive one of three interventions: a home-based exercise program performed twice daily for four weeks, instrument-assisted soft tissue mobilization administered twice a week for eight sessions, or percussion massage therapy administered twice a week for eight sessions. The treatments aim to improve pain, functionality, and kinesiophobia related to lumbar disc herniation.

Twice weekly visits for 8 sessions or daily home exercises with weekly phone follow-up

Trial Site Locations

Total: 1 location

1

Istanbul Medipol University

Istanbul, Turkey (Türkiye), 34820

Actively Recruiting

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Research Team

İ

İlayda Gundogmus

B

Burak Menek, PhD

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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