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Clinical Trials/NCT06113185
NCT06113185
Recruiting
Not Applicable

Turkish Psychometric Properties of Pain Behavior Scale in Patients With Chronic Low Back Pain

Acibadem University1 site in 1 country100 target enrollmentFebruary 21, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Low Back Pain
Sponsor
Acibadem University
Enrollment
100
Locations
1
Primary Endpoint
Pain Behavior Scale
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The aim of this study was to examine the Turkish validity of the Pain Behavior Scale in a population with chronic non-specific low back pain and to examine both intra-rater and inter-rater reliability. In addition, since this test package includes a series of functional activities, it is aimed to assess pain behaviors during functional movement in this population and to verify the test-retest reliability of physical performance tests.

Detailed Description

To assess the extent to which individuals with chronic low back pain are affected during functional task performance, the presence or absence of pain behaviors and the severity of observed pain behavior should be considered. The Pain Behavior Scale has potential clinical application both for assessing pain behaviors during regular physical examination and for measuring the presence and severity of pain behaviors during functional movement. There is no similar assessment tool that offers all of these simultaneously. Therefore, this study aimed to examine the Turkish validity of the Pain Behavior Scale in a population with chronic non-specific low back pain and to test its intra- and inter-rater reliability.

Registry
clinicaltrials.gov
Start Date
February 21, 2024
End Date
January 2025
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Acibadem University
Responsible Party
Sponsor

Eligibility 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

Outcomes

Primary Outcomes

Pain Behavior Scale

Time Frame: At the beginning of the study and up to 1 weeks

The Pain Behavior Scale was developed to record the presence and severity of pain behaviors exhibited during physical performance tests. Specific pain behaviors assessed are sighing, breath holding, grimacing, guarding, rubbing and antalgic gait. The Pain Behavior Scale consists of a 4-point scale ranging from "None" (no observed behavior) to "Severe" (marked pain behavior). Two measures are obtained from the scale 1. The presence or absence of each behavior 2. Total score for the severity of general pain behaviors. The scale will be used during the implementation of physical performance tests lasting 10-15 minutes.

Visual Analog Scale

Time Frame: At the beginning of the study

The Visual Analog Scale, which is used to record the intensity of pain, consists of a single 10 cm line; the left end is described as "No pain" and the right end is described as "The most severe pain experienced in life". Patients will be asked to mark the severity of their current pain on the 10 cm line. During the calculation, the marked point will be measured in cm. The higher the score, the more severe the pain.

McGill Pain Questionnaire-Short Form

Time Frame: At the beginning of the study

The McGill Pain Questionnaire Short Form consists of three parts. In the first part, patients are asked to describe their pain with 15 descriptive words (11 sensory and 4 affective). In the second part, the severity of the patient's pain is evaluated. In the third part, patients are asked to mark their current pain intensity on a visual comparison scale.

Secondary Outcomes

  • Fear-Avoidance Beliefs Questionnaire(At the beginning of the study)
  • Oswestry Disability Index(At the beginning of the study)

Study Sites (1)

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