About this trial
Chronic neck pain is a common health condition that causes disability and functional limitations, and while clinicians frequently rely on patient-reported questionnaires to assess symptoms, it remains unclear how accurately these self-reported measures reflect actual physical capacity. This study aims to investigate the relationship between patient-reported outcome measures and objective physical performance assessments in 98 women aged 18-45 years with chronic nonspecific neck pain. Participants will complete questionnaires evaluating perceived neck mobility (S-ROM-Neck), fear of movement (Tampa Scale for Kinesiophobia), and pain intensity (Visual Analog Scale), which will be compared against objective measurements including active cervical range of motion using a CROM device, controlled box-lifting capacity (PILE test), timed unloaded and loaded walking performance, and deep cervical flexor and extensor muscle endurance tests. Ultimately, the findings will clarify whether self-reported questionnaires are sufficient for evaluating physical capacity or if objective performance testing should be routinely integrated into clinical practice
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Presence of chronic nonspecific neck pain lasting for at least 3 months,
Ability to understand test instructions and complete self-reported questionnaires,
Willingness to participate in all physical performance and range of motion assessments,
Voluntary provision of written informed consent.
Disqualifiers
Specific cervical spine pathologies, including cervical radiculopathy, myelopathy, or severe spinal stenosis,
History of cervical spine surgery or severe neck trauma/fracture,
Inflammatory, systemic, or autoimmune diseases affecting the musculoskeletal system (e.g., rheumatoid arthritis, ankylosing spondylitis),
Neurological, neuromuscular, or vestibular disorders that impair balance, coordination, or strength,
Trial population
Female participants recruited from outpatient physical therapy and rehabilitation clinics, university campus announcements, and local community health networks.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Objective Cervical Range of Motion Measured by Cervical Range of Motion (CROM) Device.
Active cervical range of motion in degrees (°).
Perceived Cervical Range of Motion (S-ROM-Neck)
Pain Intensity Evaluated by Visual Analog Scale (VAS).
Secondary outcomes
Functional Lifting Capacity Evaluated by Progressive Isoinertial Lifting Evaluation (PILE) Test.
Unloaded Walking Speed Evaluated by 2x20-Meter Walking Test.
Deep Cervical Flexor Muscle Endurance Evaluated by Cranio-Cervical Flexion Test
Deep Cervical Extensor Muscle Endurance Test.
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Borna Farhoomand
Lead sponsor
Pamukkale University
Sponsor institution
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