Actively Recruiting
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
Eligibility Criteria
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
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
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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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