Examining a Pain Scale for Chronic Low Back Pain
Turkish Psychometric Properties of Pain Behavior Scale in Patients With Chronic Low Back Pain
This study is testing a new pain scale to see how well it works for people with chronic low back pain in Turkey.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 18 Years to 55 Years |
| Sex | All |
| Sponsor | Acibadem University Academic / other |
| Locations | 1 site (Istanbul, None Selected) |
| Trial ID | NCT06113185 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the Turkish validity of the Pain Behavior Scale specifically for individuals suffering from chronic non-specific low back pain. It will assess both intra-rater and inter-rater reliability, as well as the presence and severity of pain behaviors during functional movements. The study will utilize a survey approach to gather data on pain behaviors and physical performance tests, providing a comprehensive assessment tool that has not been previously available in this context.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-55 who have experienced non-specific low back pain for more than three months.
Not a fit: Patients with serious underlying pathologies, spinal stenosis, or those who are pregnant will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved assessment and management of chronic low back pain through a validated pain behavior scale.
How similar studies have performed: While this approach is novel in the Turkish context, similar studies have shown success in validating pain assessment tools in other populations.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Non-specific low back pain for more than three months * Being between the ages of 18-55 * Adequate cognitive functions (reading, writing, recall, orientation, language) Exclusion Criteria: * Presence of a serious underlying pathology (e.g. cancer, infection or cauda equina syndrome) * Presence of spinal stenosis * Presence of signs of radiculopathy (presence of neural symptoms such as pain radiating to the lower extremities, weakness, numbness and tingling sensation) * Presence of fracture or surgical history in the relevant area * Presence of rheumatic disease history * Presence of pregnancy
Where this trial is running
Istanbul, None Selected
- Acıbadem Health Group — Istanbul, None Selected, Turkey (Türkiye) (Recruiting)
Study contacts
- Principal investigator: Elif E Safran, asst. prof. — Acibadem Healthcare Group
- Study coordinator: Elif E Safran, asst. prof.
- Email: elif.bayraktar@acibadem.edu.tr
- Phone: 500 4047
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.