Actively Recruiting
Comparison of the Effectiveness of Mobilization and Myofascial Release Techniques in Patients With Sacroiliac Joint Dysfunction
Led by Kirsehir Ahi Evran Universitesi · Updated on 2026-02-27
42
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Sacroiliac joint dysfunction (SIED) is one of the major causes of chronic mechanical low back pain and is associated with pain, postural control impairment, and functional limitations. While manual therapy approaches are commonly used in the treatment of sacroiliac joint pain, evidence regarding the clinical superiority of different manual techniques is limited. This study was designed as a prospective, randomized controlled trial to compare the effects of myofascial release techniques and sacroiliac joint mobilizations, applied in addition to a traditional physical therapy program, on pain intensity, spinal mobility, postural control, and functional status in women diagnosed with sacroiliac joint dysfunction. The study plans to include female individuals aged 18-65 years with a Visual Analog Scale (VAS) score ≥3 who have been diagnosed with sacroiliac joint dysfunction according to international diagnostic criteria. Participants will be randomly assigned to two groups: one group will receive traditional treatment combined with myofascial release techniques, while the other group will receive traditional treatment combined with sacroiliac joint mobilizations. Interventions will be performed three days per week for six weeks. Primary and secondary outcome measures will include pain intensity (VAS), postural control (Biodex Balance System), spinal mobility, and postural endurance (Spinal Mouse) assessments. Participants will be randomly assigned to two groups: one group will receive traditional treatment combined with myofascial release techniques, while the other group will receive traditional treatment combined with sacroiliac joint mobilizations. Interventions will be performed three days a week for six weeks. Primary and secondary outcome measures will include pain intensity (VAS), postural control (Biodex Balance System), spinal mobility, and postural endurance (Spinal Mouse) assessments. All assessments will be conducted before treatment and at the end of the six-week intervention period. This study aims to provide clinical evidence regarding the comparative effectiveness of manual therapy approaches in the conservative treatment of sacroiliac joint dysfunction and to contribute to clinical decision-making processes.
CONDITIONS
Official Title
Comparison of the Effectiveness of Mobilization and Myofascial Release Techniques in Patients With Sacroiliac Joint Dysfunction
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female individuals aged 18 to 65 years
- Diagnosed with sacroiliac joint dysfunction based on International Association for the Study of Pain criteria
- Localized pain in the sacroiliac joint region, possibly radiating to hip, groin, or lower limbs
- Positive in at least 3 out of 5 sacroiliac joint-specific provocation tests
- Pain intensity of 3 or higher on the Visual Analog Scale (VAS)
- Willingness to participate and provide written informed consent
You will not qualify if you...
- History of surgery involving the spine, pelvis, or lower extremities
- Presence of lumbar disc herniation, spinal stenosis, or acute hip joint pathologies
- Diagnosis of piriformis syndrome or low back/hip pain from other sources than sacroiliac joint
- Known central or peripheral nervous system disease or progressive neurological deficit
- History of rheumatological diseases such as rheumatoid arthritis or ankylosing spondylitis
- Pregnancy or serious systemic disease preventing study participation
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Trial Site Locations
Total: 1 location
1
Kirşehir Ahi Evran University
Center, Kirşehi̇r, Turkey (Türkiye)
Actively Recruiting
Research Team
Ş
Şafak KUZU, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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