Effects of IASTM and Vibration Therapy on Neck Pain from Cervical Disc Herniation
Effects of Instrument-Assisted Soft Tissue Mobilization and Vibration Therapy on Pain, Functional Status, Proprioception, and Kinesiophobia in Individuals With Cervical Disc Herniation
NA · Medipol University · NCT06903000
This study is testing whether instrument-assisted soft tissue therapy or vibration therapy can help people with neck pain from a herniated disc feel better and move more easily compared to regular exercise.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 66 (estimated) |
| Ages | 30 Years to 60 Years |
| Sex | All |
| Sponsor | Medipol University (other) |
| Locations | 1 site (Istanbul, Beykoz) |
| Trial ID | NCT06903000 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of instrument-assisted soft tissue mobilization (IASTM) and vibration therapy on pain and functionality in individuals with cervical disc herniation. A total of 66 participants will be randomly assigned to one of three groups: vibration therapy, IASTM, or conventional exercise. All groups will receive standard physiotherapy, while the intervention groups will also receive their respective therapies. The effectiveness of these approaches will be evaluated using various outcome measures, including pain scales and functional assessments.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals diagnosed with cervical disc herniation who have experienced neck pain for at least three weeks.
Not a fit: Patients with additional orthopedic or neurological disorders, or those who have received physiotherapy in the past six months, may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide effective non-surgical treatment options for patients suffering from neck pain due to cervical disc herniation.
How similar studies have performed: Other studies have shown promising results with similar therapeutic approaches, indicating potential for success in this study.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Have a diagnosis of cervical disc herniation. * Have a complaint of neck pain lasting at least 3 weeks. * Have a restriction in cervical range of motion. Exclusion Criteria: * Have any additional orthopedic or neurological disorders besides cervical problems. * Have a history of previous trauma to the cervical region. * Have received physiotherapy within the past 6 months. * Are unable to tolerate vibration therapy.
Where this trial is running
Istanbul, Beykoz
- Emre Dansuk — Istanbul, Beykoz, Turkey (RECRUITING)
Study contacts
- Principal investigator: Emre Dansuk, PhD — Medipol University
- Study coordinator: Emre Dansuk, PhD
- Email: edansuk@medipol.edu.tr
- Phone: +9053377790434
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Intervertebral Disc Displacement, Neck Pain, Cervical disc herniation, Neck pain, Instrument-assisted soft tissue mobilization, Vibration therapy, Proprioception, Kinesiophobia