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Not yet recruiting NCT07033377

Psychometric Validation of Persian CBQ-NSCLBP

Observational Nonspecific Chronic Low Back Pain

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: Self-administered paper-based questionnaires.
Who it may be relevant to
Registry conditions: Nonspecific Chronic Low Back Pain. Basic parameters: 18 years — 65 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
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Cross-Cultural Adaptation and Psychometric Validation of the Persian Version of the Cognitive Behavioral Questionnaire in Nonspecific Chronic Low Back Pain

Overview

This study aims to translate, culturally adapt, and psychometrically validate the Persian version of the Cognitive Behavioral Questionnaire in Nonspecific Chronic Low Back Pain (CBQ-NSCLBP). The process will follow standard cross-cultural adaptation guidelines, including forward-backward translation, expert review, and pilot testing. The psychometric properties, including internal consistency, test-retest reliability, and construct validity, will be evaluated in a sample of Persian-speaking adults with nonspecific chronic low back pain.

Detailed description

Chronic low back pain (CLBP) is a common and persistent musculoskeletal condition that affects a large portion of the population and can lead to long-term disability. It is typically defined as pain in the lower back that lasts for more than 12 weeks and often impacts daily function and quality of life.

In addition to physical symptoms, people with CLBP frequently experience cognitive and behavioral challenges, such as fear-avoidance beliefs, catastrophizing, and difficulty concentrating. These factors can contribute to ongoing disability and interfere with the rehabilitation process.

The Cognitive Behavioral Questionnaire for Nonspecific Chronic Low Back Pain (CBQ-NSCLBP) was developed to assess these cognitive-behavioral aspects in people with nonspecific CLBP. However, it has only been validated in one population and has not yet been adapted for Persian-speaking individuals.

This study aims to translate and culturally adapt the CBQ-NSCLBP into Persian and evaluate its psychometric properties in individuals with nonspecific chronic low back pain

Interventions

  • Other Self-administered paper-based questionnaires
    Participants will complete the Persian version of the CBQ-NSCLBP and other self-report measures as part of a psychometric validation study. No clinical or therapeutic intervention is involved.

Primary outcome measures

  • CBQ-NSCLBP [Time frame: Baseline and within 6 to 10 days after enrollment]

Eligibility criteria

Inclusion criteria

  • Age between 18 - 65 years old.
  • Experiencing nonspecific low back pain for at least 6 months.
  • Have a physician-confirmed diagnosis.
  • Be able to read and understand Persian.
  • Be willing to participate and provide written informed consent.

Exclusion criteria

  • Specific causes of low back pain (e.g., spinal infection, tumor, fracture, inflammatory disease, radiculopathy, or other neurological disorders).
  • Severe psychiatric disorders or cognitive impairments interfering with questionnaire comprehension.
  • History of surgery for low back pain.
  • Abnormal bowel or bladder function.
  • Pregnant at the time of participation.
  • Not fluent in Persian.

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
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07033377 · MEDI-CBQNSCLBP-Pe

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗