[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cervical-pain\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cervical-pain":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,48,80,108,130,149,170],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":31,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100635425","patient-reported-outcome-measurements-registration-in-spinal-pathologies-and-neuromodulation-100635425",false,"NCT07552519","Patient Reported Outcome Measurements Registration in Spinal Pathologies and Neuromodulation","Patient Reported Outcome Measurements Registration in Spinal Pathologies and Neuromodulation: a Prospective Real-world Data Collection With Pre-determined Follow-up Moments","PROMSPINE","Inclusion Criteria:\n\n1. Clinical diagnosis of spinal disease\n2. Clinical indication to perform treatment of this disease\n3. willing and capable to provide informed consent\n4. Age ≥18 y\n\nExclusion Criteria:\n\nnot able to provide consent","ALL","18 Years",{"count":20,"type":21},5000,"ESTIMATED","OBSERVATIONAL","Longitudinal prospective observational data collection with questionnaires and categorical diagnostic and therapeutic registration and follow-up in spinal pathologies and neuromodulation",[25,26,27,28,29,30],"Spinal Pathologies","Pain","Cervical Pain","Lumbar Pain Syndrome","Neurostimulation","Disc Degenerative Disease",[32,33,34],"neuromodulation","pain","spinal pathologies","RECRUITING","2026-04-20",{"date":38,"type":39},"2026-04-27","ACTUAL",{"date":41,"type":21},"2026-04",{"date":43,"type":21},"2030-06-01",{"name":45,"class":46},"Jessa Hospital","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":47},"100597417","effect-cervical-proprioceptive-training-cervical-proprioception-neck-pain-100597417","NCT07058220","Effect Cervical Proprioceptive Training Cervical Proprioception Neck Pain:","Physical Therapist at 23 July Hospital Marg Egypt","Inclusion Criteria:\n\n* they had non-specific neck pain\n\nExclusion Criteria:\n\n* they had positive spurling test.","25 Years","45 Years",{"count":58,"type":21},25,"INTERVENTIONAL",[61],"NA","Twenty-two male and female patients with neck pain participated in this study, aged from 25-40 years. They randomly distributed into 2 group: group (A, study) consisted of 11 patients received cervical proprioceptive training, while group (B, control) consisted of 11 patients received usual care. The treatment was performed 3 times per week for 1 month. The cervical proprioception (flexion, extension, right and left rotations) was assessed by Revel laser method as active joint angular reproduction \\[absolute error\\].",[64,27],"Cervical Joint Position Error",[66,67,68,69,70],"neck pain","cervical proprioception","training","exercise","proprioceptive error","2025-07-05",{"date":73,"type":39},"2025-07-10",{"date":75,"type":39},"2025-04-01",{"date":77,"type":21},"2025-09-01",{"name":79,"class":46},"Cairo University",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":87,"sex":17,"minAge":18,"maxAge":88,"enrollmentInfo":89,"targetDuration":4,"studyType":59,"phases":91,"briefSummary":92,"conditions":93,"keywords":96,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":47},"100521420","predictors-of-response-to-manual-physiotherapy-using-somatosensory-profiles-in-patients-with-cervicobrachial-pain-100521420","NCT06069362","Predictors of Response to Manual Physiotherapy Using Somatosensory Profiles in Patients With Cervicobrachial Pain","Prediction of Response to Manual Physiotherapy Using Somatosensory Profiles in Patients With Cervicobrachial Pain","Inclusion Criteria:\n\n* Subjects with unilateral cervicobrachial pain\n\nExclusion Criteria:\n\n* Signs of severe disease, cervical myelopathy, tumour, rheumatic diseases or a neurological pathology of central origin.\n* Cervicobrachial pain of traumatic origin or as a result of whiplash.\n* Previous surgical intervention of the cervical spine.",true,"80 Years",{"count":90,"type":21},91,[61],"The goal of this clinical trial is to investigate about the characteristics that predict response to physiotherapy treatment in patients with nerve related neck arm pain. The main question to answer is whether there is a subgroup that responds better to physiotherapy treatment.\n\nParticipants will be assessed for clinical and neurophysiological characteristics prior to treatment. Afterwards they will receive 6 sessions of manual physiotherapy treatment along with home nerve gliding exercises once a week. Baseline measurements will be taken again after treatment to know if there have been any changes.",[94,95,27],"Cervical Radicular Pain","Cervical Radiculopathy",[97,98],"Cervicobrachial pain","Nerve related neck arm pain","2025-03-25",{"date":101,"type":39},"2025-03-26",{"date":103,"type":39},"2023-04-20",{"date":105,"type":21},"2025-07-20",{"name":107,"class":46},"University of Deusto",{"id":109,"slug":110,"hasResults":11,"nctId":111,"briefTitle":112,"officialTitle":112,"acronym":4,"eligibilityCriteria":113,"healthyVolunteers":11,"sex":114,"minAge":115,"maxAge":116,"enrollmentInfo":117,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":119,"conditions":120,"keywords":4,"overallStatus":121,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":125,"completionDateStruct":127,"leadSponsor":129,"locationsCount":47},"100573079","biomechanical-risk-factors-of-cervical-pain-in-pregnant-women-100573079","NCT06741605","Biomechanical Risk Factors of Cervical Pain in Pregnant Women","Inclusion Criteria:\n\n* Pregnant women in their third trimester suffering from cervical pain.\n* They have experienced cervical pain starting during pregnancy.\n* They reported no neck pain or neck-related disorders during the previous year and were screened for the absence of cervical pathology during a physical examination.\n\nExclusion Criteria:\n\n* Objective signs of structural pathology on physical examination, including but not limited to shoulder bursitis, impingement, tendonitis, fracture, cervical nerve or disc impairment, radiculopathy, or loss of upper extremity sensory or motor function.\n* Acute injury of the neck or shoulders (\\\u003C12 weeks before the study).\n* History of fibromyalgia or musculoskeletal pain present in more than 4 body regions concurrently.\n* Self-reported systemic illness, including cancer, rheumatic, cardiovascular, or neurological disease\n* Untreated psychiatric condition\n* Previous surgery involving the cervical spine or shoulders\n* Uncontrolled hypertension (resting systolic blood pressure \\>150 mm Hg, or diastolic blood pressure \\>90 mm Hg).","FEMALE","20 Years","35 Years",{"count":118,"type":21},116,"The purpose of the study is to assess the biomechanical risk factors for neck pain in pregnant women.",[27],"NOT_YET_RECRUITING","2024-12-15",{"date":124,"type":39},"2024-12-19",{"date":126,"type":21},"2024-12-20",{"date":128,"type":21},"2025-03-01",{"name":79,"class":46},{"id":131,"slug":132,"hasResults":11,"nctId":133,"briefTitle":134,"officialTitle":134,"acronym":4,"eligibilityCriteria":135,"healthyVolunteers":87,"sex":17,"minAge":55,"maxAge":116,"enrollmentInfo":136,"targetDuration":4,"studyType":59,"phases":138,"briefSummary":139,"conditions":140,"keywords":4,"overallStatus":121,"whyStopped":4,"lastUpdateSubmitDate":141,"lastUpdatePostDateStruct":142,"startDateStruct":144,"completionDateStruct":146,"leadSponsor":148,"locationsCount":4},"100554089","effect-of-cervical-stabilization-exercises-on-proprioception-and-hand-grip-strength-in-sedentary-office-workers-100554089","NCT06494553","Effect of Cervical Stabilization Exercises on Proprioception and Hand Grip Strength in Sedentary Office Workers","Inclusion Criteria:\n\n* Age range between 25 and 35 years.\n* Both male and female patients were included.\n* Informed consent was obtained from all participants.\n* Subjects with cervical pain lasting for more than 3 months (chronic pain).\n* Cooperative patients who were able to follow instructions for assessment procedures.\n* body mass index (18.5 - 29.99 Kg\u002Fm2).\n\nExclusion Criteria:\n\n* Unwillingness to participate in the treatment.\n* Pre-existing heart or respiratory diseases.\n* Acute cervical pain.\n* Cervical disc or spondylosis.\n* History of any major cervical spine surgery.\n* Subjects taking analgesics.\n* Any fracture of cervical region.",{"count":137,"type":21},52,[61],"The purpose of the study is to evaluate the effect of cervical stabilization exercises on pain intensity level, cervical range of motion, proprioception, and handgrip strength in sedentary office workers.",[27],"2024-07-02",{"date":143,"type":39},"2024-07-10",{"date":145,"type":21},"2024-07",{"date":147,"type":21},"2024-10",{"name":79,"class":46},{"id":150,"slug":151,"hasResults":11,"nctId":152,"briefTitle":153,"officialTitle":154,"acronym":4,"eligibilityCriteria":155,"healthyVolunteers":11,"sex":17,"minAge":156,"maxAge":18,"enrollmentInfo":157,"targetDuration":4,"studyType":59,"phases":159,"briefSummary":160,"conditions":161,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":162,"lastUpdatePostDateStruct":163,"startDateStruct":165,"completionDateStruct":166,"leadSponsor":168,"locationsCount":47},"100553892","chitosan-phonophresis-on-cervical-in-smartphone-addicted-users-100553892","NCT06491992","Chitosan Phonophresis on Cervical IN Smartphone Addicted Users","Effect of Chitosan Phonophresis on Cervical Pain and Disability in Smartphone Addicted Users","Inclusion Criteria:\n\n* Their age will be ranged from 16-18 years\n* body mass index will be 26.58 kg\u002Fm2.\n* used a smart phone for more than 1 year for at least 2 hours per day\n* complaining of neck pain after using a smart phone, addiction to smart phone in accordance with the smart phone addiction scale (SAS)\n\nExclusion Criteria:\n\n* any previous head and neck injuries or surgeries\n* any congenital abnormalities or symptomatic deformity in either the cervical or the lumbar spine\n* any uncorrected visual or auditory problems, dizziness, vertigo and headache\n* any systematic diseases, any addiction to alcohol, any additive drugs and sedatives within 48 hours previous to tests\n* body mass index of subjects over25 kg\u002Fm2.","16 Years",{"count":158,"type":21},30,[61],"A phonophoresis-based drug delivery system is a synchronous approach to improve local drug penetration in neuromuscular diseases associated with neuronal damage, excruciating pain, and local inflammation. Chitosan, a semi-synthetic material, is obtained by partial deacetylation of chitin amines, resulting in copolymers of N-acetylglucosamine and N-glucosamine. Its use has been explored in various biomaterial and medical applications. Chitosan has emerged as a cost-effective, biocompatible, and biodegradable material with many desirable biological properties, improvement of homeostasis and antiviral potential. Chitosan was found to suppress pro-inflammatory cytokines and decreased peripheral nerve edema, the polycationic nature of chitosan allows it to absorb protons, which reduces inflammation and provides an analgesic effect.",[27],"2024-07-01",{"date":164,"type":39},"2024-07-09",{"date":162,"type":21},{"date":167,"type":21},"2024-10-15",{"name":169,"class":46},"October 6 University",{"id":171,"slug":172,"hasResults":11,"nctId":173,"briefTitle":174,"officialTitle":175,"acronym":4,"eligibilityCriteria":176,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":177,"enrollmentInfo":178,"targetDuration":4,"studyType":59,"phases":180,"briefSummary":181,"conditions":182,"keywords":184,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":188,"lastUpdatePostDateStruct":189,"startDateStruct":191,"completionDateStruct":193,"leadSponsor":194,"locationsCount":47},"100546608","combined-effects-of-virtual-reality-and-motor-imagery-in-patients-with-non-specific-neck-pain-100546608","NCT06397157","Combined Effects of Virtual Reality and Motor Imagery in Patients With Non-specific Neck Pain","Combined Effects of Virtual Reality and Motor Imagery With Routine Physical Therapy in Patients With Non-specific Neck Pain","Inclusion Criteria:\n\n* Age of the patients should be 18-50 years\n* Both females and males are included\n* Patient should have a consistent pain for 3 months or more.\n* Patient having non-specific neck pain.\n\nExclusion Criteria:\n\n* Specific neck pain caused by metastasis, neoplasia, infectious or inflammatory disorders, bone fractures or traumatic precedents with neck injuries (2)\n* Positive neurological signs or evidence of spinal compression (abnormal diffuse sensitivity, hyperreflexia, or diffuse weakness)\n* Cervical osteoarthritis\n* Spondylarthritis\n* Neck pain associated with vertigo (vestibular involvement)\n* Neck pain associated with whiplash injuries\n* Previous cervical surgeries (2)\n* Headaches before the onset of neck pain and without cervical origin\n* Inability to provide informed consent","50 Years",{"count":179,"type":21},93,[61],"Non-specific neck pain is the most common musculoskeletal symptom which can cause limited cervical mobility, impaired functional status and stress at work. Virtual reality and motor imagery are unique technologies which have beneficial effects on the treatment of non-specific neck pain. Virtual reality is a simulated 3D environment that enables users to explore and interact with a virtual surrounding while motor imagery (MI) is a dynamic mental process of an action, without its actual motor execution. This study aims to investigate the combined effects of Virtual Reality (VR) and Motor Imagery Techniques (MI) with Routine Physical Therapy (RPT) in patients with Non-specific neck pain. This randomized clinical trial will be carried at Railway General Hospital, Rawalpindi on 93 participants meeting the inclusion criteria included in the study through probability convenience sampling technique. 3 groups of participants assigned ramdomly will receive interventions for three days a week for 6 weeks. Group A will receive virtual reality (VR) and motor imagery (MI) along with routine physical therapy for . Group B participants will receive VR along with routine physical therapy while Group C will receive MI along with routine physical therapy. Total treatment time will be 40 minutes. Outcome measure tools will be Numeric pain rating scale to measure pain, the Tampa scale of Kinesiophobia (TSK) for the measurement of kinesiophobia and Neck disability index for disability and functional status.",[27,183,26],"Kinesiophobia",[185,183,26,186,187],"Cervical pain","Motor Imagery","Virtual Reality","2024-06-11",{"date":190,"type":39},"2024-06-13",{"date":192,"type":39},"2023-12-10",{"date":143,"type":21},{"name":195,"class":46},"Riphah International University"]