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Relationship between increased pain sensitivity, knee alignment, pain, and disability in people with sacroiliac joint dysfunction

Evaluating Central Sensitization And Its Association With Pain, Q Angle And Disability Using Denver SI Joint Questionnaire In Sacroiliac Joint Dysfunction: A Diagnostic And Correlational Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/06/113075
Enrollment
93
Registered
2026-06-24
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M545- Low back pain

Interventions

Intervention1: NIL: NIL Intervention2: Nil: Nil Control Intervention1: NIL: NIL

Sponsors

Justice K.S Hegde Charitable Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Both male and female participants aged between 20 50 years. 2) Able to understand instructions and provide informed consent. 3) Presenting with lower back or buttock pain with or without radiation to lower extremities for greater than or equal to 3 months 4) Reporting a pain intensity of 4-7 on the Numerical Pain Rating Scale (NPRS) 5) Presence of pain or local tenderness around posterior superior iliac spine (PSIS) Positive findings in atleast 3 out of 5 pain provocation tests: Distraction, Compression, Thigh thrust, Gaenslen s test and Sacral thrust.

Exclusion criteria

Exclusion criteria: 1) Pregnant women 2) Low back pain with centralization 3) Sacrolitis in inflammatory spondyloarthropathies, rheumatoid arthritis and ankylosing spondylitis 4) History of lumbar or hip surgery or significant pathology 5) Diagnosed lumbar disc herniation, spondylolisthesis, spinal stenosis, or vertebral fracture 6) Presence of inflammatory, neurological or metabolic disorders (rheumatoid arthritis, multiple sclerosis, diabetic neuropathy) 7) Diagnosed psychiatric conditions or any vestibular disorders

Design outcomes

Primary

MeasureTime frame
Central Sensitization Inventory (CSI)Timepoint: one time baseline assessment

Secondary

MeasureTime frame
Numeric Pain Rating Scale (NPRS), Denver Sacroiliac Joint Questionnaire (DSIJQ), Q-angle measurementTimepoint: one time baseline assessment

Countries

India

Contacts

Public ContactDr Saumya Srivastava

Nitte Institute of Physiotherapy

saumyasri2000@nitte.edu.in9740244077

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026