Comparing Patient-Reported Symptoms to Objective Neck Range of Motion and Physical Capacity in Women With Chronic Neck Pain.

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorBorna Farhoomand

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

96 Participants
are grouped into 1 trial group
Group A: Women with Chronic Nonspecific Neck Pain

Trial outcomes

Primary outcomes

1

Objective Cervical Range of Motion Measured by Cervical Range of Motion (CROM) Device.

Active cervical range of motion in degrees (°).

Time frame
Baseline (Single evaluation session).
2

Perceived Cervical Range of Motion (S-ROM-Neck)

Time frame
Baseline (Single evaluation session)
3

Pain Intensity Evaluated by Visual Analog Scale (VAS).

Time frame
Baseline (Single evaluation session).

Secondary outcomes

1

Functional Lifting Capacity Evaluated by Progressive Isoinertial Lifting Evaluation (PILE) Test.

Time frame
Baseline (Single evaluation session).
2

Unloaded Walking Speed Evaluated by 2x20-Meter Walking Test.

Time frame
Baseline (Single evaluation session).
3

Deep Cervical Flexor Muscle Endurance Evaluated by Cranio-Cervical Flexion Test

Time frame
Baseline (Single evaluation session).
4

Deep Cervical Extensor Muscle Endurance Test.

Time frame
Baseline (Single evaluation session).

Other outcomes

Locations

This trial has no 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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