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Recruiting NCT06869668

The Relationship Between Disability, Fear Avoidance Beliefs, Physical Performance and Quality of Life in Chronic Low Back Pain

Observational Low Back Pain Chronic Low-back Pain (cLBP)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Correlation.
Who it may be relevant to
Registry conditions: Low Back Pain, Chronic Low-back Pain (cLBP). Basic parameters: 18 years — 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The aim of this study was to determine the multidimensional profile of individuals with chronic low back pain (CLBP) and to determine the relationship between disability and fear avoidance beliefs, physical performance and quality of life in this population. Individuals with chronic low back pain between the ages of 18-50 will be included in the study. Disability level of the participants will be assessed with Oswestry Disability Index (ODI), fear avoidance attitudes with Avoidance Beliefs Questionnaire-Physical Activity (FABQ-PA), and quality of life with Short Form-12 (SF-12). Trunk endurance, functional mobility and static-dynamic balance will be assessed for physical performance. Trunk endurance will be assessed with McGill endurance tests, functional mobility with Timed Up and Go Test (TUG), dynamic balance with Y-balance test, and static balance with single leg stance test.

Interventions

  • Other Correlation
    Correlation between outcomes

Primary outcome measures

  • Oswestry Disability Index (ODI) [Time frame: Day 1]
  • Fear Avoidance Beliefs Questionnaire [Time frame: Day 1]
  • Short Form-12/SF-12 [Time frame: Day 1]
  • McGill Trunk Muscle Endurance Tests [Time frame: Day 1]
  • Timed Up and Go Test (TUG) [Time frame: Day 1]
  • Y balance test [Time frame: Day 1]
  • Single leg stance test [Time frame: Day 1]
  • Visual Analog Scale [Time frame: Day 1]

Eligibility criteria

Inclusion criteria

  • Back pain for at least 3 months
  • Pain intensity ≥ 3 on the Visual Analog Scale

Exclusion criteria

  • History of spinal surgery/trauma
  • Other back pain (associated with rheumatic diseases, multiple sclerosis, malignancy, etc.) instability conditions such as spondylolysis and spondylolisthesis
  • Pregnancy
  • Obesity (BMI ≥ 30 kg/m²)
  • Presence of orthopedic problems or chronic diseases that may interfere with testing

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Turkey (Türkiye) · 1 center
  • Istanbul University-Cerrahpasa — Istanbul

Identifiers

NCT: NCT06869668 · takgullereker

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗