[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100659263":3},{"organization":4,"outcomesModule":7,"designInfo":30,"detailedDescription":15,"studyPopulation":33,"armGroups":34,"interventions":15,"overallOfficials":15,"centralContacts":15,"locations":15,"responsibleParty":37,"collaborators":15,"id":41,"slug":42,"hasResults":43,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":15,"eligibilityCriteria":47,"healthyVolunteers":43,"sex":48,"minAge":49,"maxAge":50,"enrollmentInfo":51,"targetDuration":15,"studyType":54,"phases":15,"briefSummary":55,"conditions":56,"keywords":15,"overallStatus":59,"whyStopped":15,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":64,"completionDateStruct":65,"leadSponsor":67,"locationsCount":15},{"fullName":5,"class":6},"Pamukkale University","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":19,"otherOutcomes":15},[9,13,17],{"measure":10,"description":11,"timeFrame":12},"Objective Cervical Range of Motion Measured by Cervical Range of Motion (CROM) Device.","Active cervical range of motion in degrees (°).","Baseline (Single evaluation session).",{"measure":14,"description":15,"timeFrame":16},"Perceived Cervical Range of Motion (S-ROM-Neck)",null,"Baseline (Single evaluation session)",{"measure":18,"description":15,"timeFrame":12},"Pain Intensity Evaluated by Visual Analog Scale (VAS).",[20,22,24,26,28],{"measure":21,"description":15,"timeFrame":12},"Functional Lifting Capacity Evaluated by Progressive Isoinertial Lifting Evaluation (PILE) Test.",{"measure":23,"description":15,"timeFrame":12},"Unloaded Walking Speed Evaluated by 2x20-Meter Walking Test.",{"measure":25,"description":15,"timeFrame":12},"Deep Cervical Flexor Muscle Endurance Evaluated by Cranio-Cervical Flexion Test",{"measure":27,"description":15,"timeFrame":12},"Deep Cervical Extensor Muscle Endurance Test.",{"measure":29,"description":15,"timeFrame":12},"Fear of Movement Evaluated by Tampa Scale for Kinesiophobia (TSK).",{"allocation":15,"interventionModel":15,"interventionModelDescription":15,"primaryPurpose":15,"observationalModel":31,"timePerspective":32,"maskingInfo":15},"COHORT","PROSPECTIVE","Female participants recruited from outpatient physical therapy and rehabilitation clinics, university campus announcements, and local community health networks.",[35],{"label":36,"type":15,"description":15,"interventionNames":15},"Women with Chronic Nonspecific Neck Pain",{"type":38,"investigatorFullName":39,"investigatorTitle":40,"investigatorAffiliation":5,"oldNameTitle":15,"oldOrganization":15},"SPONSOR_INVESTIGATOR","Borna Farhoomand","MSc, Physiotherapist","100659263","comparing-patient-reported-symptoms-to-objective-neck-range-of-motion-and-physical-capacity-in-women-with-chronic-neck-pain-100659263",false,"NCT07862387","Comparing Patient-Reported Symptoms to Objective Neck Range of Motion and Physical Capacity in Women With Chronic Neck Pain.","Do Patient-Reported Outcomes Reflect Objective Cervical Mobility and Physical Capacity in Women With Chronic Neck Pain?","Inclusion Criteria:\n\n* Presence of chronic nonspecific neck pain lasting for at least 3 months,\n* Ability to understand test instructions and complete self-reported questionnaires,\n* Willingness to participate in all physical performance and range of motion assessments,\n* Voluntary provision of written informed consent.\n\nExclusion Criteria:\n\n* Specific cervical spine pathologies, including cervical radiculopathy, myelopathy, or severe spinal stenosis,\n* History of cervical spine surgery or severe neck trauma\u002Ffracture,\n* Inflammatory, systemic, or autoimmune diseases affecting the musculoskeletal system (e.g., rheumatoid arthritis, ankylosing spondylitis),\n* Neurological, neuromuscular, or vestibular disorders that impair balance, coordination, or strength,\n* Current pregnancy,\n* History of receiving physical therapy, manual therapy, or cervical injections within the past 3 months,\n* Severe cognitive or psychiatric disorders preventing compliance with evaluation protocols.","FEMALE","18 Years","45 Years",{"count":52,"type":53},96,"ESTIMATED","OBSERVATIONAL","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",[57,58],"Chronic Pain","Neck Pain","NOT_YET_RECRUITING","2026-10-01",{"date":62,"type":63},"2026-10-07","ACTUAL",{"date":60,"type":53},{"date":66,"type":53},"2027-02-28",{"name":39,"class":6}]