[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cervicalgia\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cervicalgia":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,47,80,107,134],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100585725","validating-a-clinical-prediction-rule-to-guide-manual-therapy-and-exercise-for-neck-pain-relief-100585725",false,"NCT06906107","Validating a Clinical Prediction Rule to Guide Manual Therapy and Exercise for Neck Pain Relief","Validation of a Clinical Prediction Rule to Identify Patients With Neck Pain Likely to Benefit From Cervical Spinal Manipulation: A Randomized Clinical Trial","Inclusion Criteria:\n\n* Ages 18 to 70\n* Primary complaint of neck pain with or without unilateral upper extremity symptoms\n* Neck Disability Index (NDI) score of 10 or greater\n* Numeric Pain Rating Scale score of 2 or greater\n\nExclusion Criteria:\n\n* History of whiplash injury within the past 6 weeks\n* Diagnosis of cervical spinal stenosis\n* Bilateral upper extremity symptoms\n* Red flags noted in the patient's Neck Medical Screening Questionnaire (i.e. tumor, fracture, rheumatoid arthritis, osteoporosis, severe atherosclerosis, dizziness, diplopia, drop attacks, bilateral numbness, nausea, prolonged history of steroid use)\n* Evidence of central nervous system involvement, to include hyperreflexia, sensory disturbances in the hand, intrinsic muscle wasting of the hands, unsteadiness during walking, nystagmus, loss of visual acuity, impaired sensation of the face, altered taste, the presence of pathological reflexes (i.e. positive Hoffman's and\u002For Babinski reflexes)\n* Two or more positive neurological signs consistent with significant nerve root compression, including any two of the following:\n\n  1. Muscle weakness involving a major muscle group of the upper extremity\n  2. Diminished upper extremity muscle stretch reflex (biceps, triceps, or brachioradialis)\n  3. Diminished or absent sensation to pinprick or light touch in any upper extremity dermatome\n* Prior neck surgery\n* Current pregnancy, pregnancy within 6 months, or currently lactating\n* Pending legal action pertaining to their neck pain\n* Currently receiving manual therapy treatment for neck pain through chiropractic or physical therapy care\n* Inability to read English at the 8th grade reading level\n* Inability to legally provide informed consent for any other reason\n* Inability to comply with the treatment and follow-up schedule","ALL","18 Years","70 Years",{"count":20,"type":21},160,"ESTIMATED","INTERVENTIONAL",[24],"NA","Neck pain is a common issue that can lead to long-term disability and lost work time for many individuals. Despite numerous studies, finding effective treatment strategies has been challenging. One possible reason for this is that treatments may not have been tested on the specific groups of people who would benefit most. A method was developed to identify people with neck pain who are likely to see significant improvements from a manipulation technique used by physical therapists, called cervical spine thrust joint manipulation. The investigators believe that patients identified as likely responders to cervical spine manipulation will show greater improvements in disability. The investigators aim to test whether this method works with different patients and therapists across the country through a multicenter randomized clinical trial. In this study, 160 patients with primary complaints of neck pain will be enrolled from 9 clinical sites. Designed with stringent criteria for inclusion, this study is a testament to our commitment to participant safety and the effectiveness of the treatment. Participants will be randomly assigned to one of two groups: (1) one group will receive 2 sessions of cervical spine manipulation followed by 3 sessions of exercise, and (2) the other group will receive 2 sessions of gentle hands-on treatment followed by 3 sessions of exercise. The primary goal is to measure changes in disability 4 weeks after starting treatment, with follow-ups after one week, 4 weeks, 3 months, and 6 months to assess both immediate and long-term effects. By providing crucial data on the reliability of our method in identifying patients who will benefit most from cervical spine manipulation, this study has the potential to significantly enhance decision-making leading to rapid improvement. Results from this study will provide clearer guidelines on the optimal use of cervical spine manipulation, potentially revolutionizing the way patients recover from neck pain.",[27,28,29],"Neck Pain Musculoskeletal","Neck Pain Treatment","Cervicalgia",[31,32,33],"neck pain","manual therapy","physical therapy","RECRUITING","2026-04-09",{"date":37,"type":38},"2026-04-14","ACTUAL",{"date":40,"type":38},"2025-06-01",{"date":42,"type":21},"2026-12-31",{"name":44,"class":45},"Baylor University","OTHER",4,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":65,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":79},"100592637","effects-of-snags--cbt-on-pain-craniovertebral-angle--disability-in-non-specific-neck-pain-100592637","NCT06996015","Effects of SNAGs & CBT on Pain, Craniovertebral Angle & Disability in Non Specific Neck Pain","Effects of SNAGs and Cognitive Behavior Therapy on Pain, Craniovertebral Angle and Disability in Patients With Non-Specific Neck Pain","Inclusion Criteria:\n\n* Age group: 18-28 Years(20)\n* Gender Group: Both male and female participants(20)\n* Individuals with a Craniovertebral angle \\\u003C53(20)\n* Individuals having grade 2 neck pain according to KNGF Guidelines.(21)\n* Individuals having localized pain or stiffness in spine or both combined between C3 and C7 without upper-limb radiculopathy(22)\n* Individual who had not received any treatment for neck pain for the last 3 months will be included in the study.\n* Patients willing to sign written consent form.\n\nExclusion Criteria:\n\n* Those who had undergone spinal surgery(23)\n* Neck pain caused by various pathologies (rheumatoid arthritis, ankylosing spondylitis, fracture, tumor, etc.)(23)\n* Nerve root compression, (23)\n* A positive vertebrobasilar artery test, (23)\n* Severe radiculopathy,(23)\n* Osteoporosis, or osteopenia(23)\n* Long-term use of corticosteroids or anticoagulants (23)","28 Years",{"count":56,"type":21},32,[24],"Non-specific neck pain is a prevalent condition causing discomfort, reduced craniovertebral angle, and disability. This randomized controlled trial will evaluate the combined effects of Sustained Natural Apophyseal Glides (SNAGs) and Cognitive Behavioral Therapy (CBT) on pain, posture, and function. Group A will receive SNAGs and CBT, while Group B will undergo SNAGs with cervical stabilization exercises, twice weekly for four weeks. Outcomes will include pain, craniovertebral angle, and disability, analyzed using SPSS.",[60,61,29,62,63,64],"Neck Pain","Cognitive Behavior Therapy","Posture","Posterior Neck Pain","Neck Pain and Forward Head Posture",[66,67,68,69],"snags","Non-Specific Neck Pain","Craniovertebral Angle","disability","2025-07-03",{"date":72,"type":38},"2025-07-04",{"date":74,"type":38},"2025-06-10",{"date":76,"type":21},"2025-12-10",{"name":78,"class":45},"Riphah International University",1,{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":16,"minAge":87,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":90,"phases":4,"briefSummary":91,"conditions":92,"keywords":93,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":79},"100572334","usg-cmbb-dsa-study-100572334","NCT06731920","USG CMBB DSA Study","The Incidence of Inadvertent Intravascular Injection During Ultrasound-guided Cervical Medial Branch Blocks: a Fluoroscopically Controlled Study","Inclusion Criteria:\n\nConsenting patients over 19 years of age undergoing an ultrasound-guided cervical medial branch blocks as part of their usual care.\n\nExclusion Criteria:\n\nSubjects with one or more of the following characteristics will be excluded from the study:\n\nKnown bleeding disorder or coagulopathy Patients on antiplatelet medication other than aspirin and those on anticoagulants (coumadin, AT III agents) Inability to visualize targeted structures on ultrasound Known allergy to contrast agents","19 Years",{"count":89,"type":21},300,"OBSERVATIONAL","Injections that freeze neck joints can be done using x-rays or ultrasound imaging, which as a newer way of guiding the needle to the right spot. This study will look at how often freezing liquid goes into a blood vessel during neck injections that freeze neck joints when ultrasound guidance is used to place the needle. When this happens, it can go undetected because it does not make the patient feel any different, however it could cause a test block to be falsely negative, leading to the wrong diagnosis. Based on previous studies, we think that this happens rarely, and the purpose of this study is to prove that conclusively",[29],[94,95,96,97],"Ultrasound","cervical medial branch block","safety","digital subtraction angiography","2024-12-11",{"date":100,"type":38},"2024-12-13",{"date":102,"type":21},"2025-01-10",{"date":104,"type":21},"2026-08",{"name":106,"class":45},"Montreal General Hospital",{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":4,"eligibilityCriteria":113,"healthyVolunteers":114,"sex":16,"minAge":17,"maxAge":115,"enrollmentInfo":116,"targetDuration":4,"studyType":22,"phases":118,"briefSummary":119,"conditions":120,"keywords":121,"overallStatus":124,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":79},"100548094","pompage-and-photobiomodulation-on-pain-range-of-motion-and-quality-of-life-in-patients-with-neck-pain-100548094","NCT06416527","Pompage and Photobiomodulation on Pain, Range of Motion, and Quality of Life in Patients With Neck Pain","Effects of Pompage Associated or Not With Photobiomodulation on Pain, Range of Motion, and Quality of Life in Patients With Neck Pain: a Controlled, Randomized, and Double Blinded Study","Inclusion Criteria:\n\n* Age between 18 and 62 years;\n* Both genders;\n* Without comorbidities.\n\nExclusion Criteria:\n\n* Presentation of rheumatic or degenerative diseases in the cervical region;\n* Undergoing orthodontic or physiotherapeutic treatment;\n* Initiation of the use of any medication during any phase of the study;\n* Using bite plate.",true,"62 Years",{"count":117,"type":21},30,[24],"The aim of this study is to evaluate the effects of Pompage associated or not with PBM, using a cluster of LEDs, on pain and neck disability. This controlled, randomized, and double-blinded clinical study includes participants of both genders, aged 18 to 55, with non-specific chronic neck pain will be included. Participants will be randomized into two groups: (1) Pompage (n=28) focusing only on manual therapy through Pompage technique and (2) Pompage + PBM Group (n=28) involving the same procedures as the first group, followed by PBM with a LED cluster applied for 10 minutes to the neck region for 10 sessions. Pain and functional disability will be assessed using the visual analog scale (VAS) and Neck Pain Disability Index before and after the intervention. The resulting data will be submitted to statistical analysis considering α=0.05.",[29],[31,122,123,32],"photobiomodulation","LED","NOT_YET_RECRUITING","2024-11-21",{"date":127,"type":38},"2024-11-25",{"date":129,"type":21},"2024-12-30",{"date":131,"type":21},"2025-03",{"name":133,"class":45},"University of Nove de Julho",{"id":135,"slug":136,"hasResults":11,"nctId":137,"briefTitle":138,"officialTitle":139,"acronym":4,"eligibilityCriteria":140,"healthyVolunteers":11,"sex":16,"minAge":141,"maxAge":142,"enrollmentInfo":143,"targetDuration":145,"studyType":90,"phases":4,"briefSummary":146,"conditions":147,"keywords":148,"overallStatus":124,"whyStopped":4,"lastUpdateSubmitDate":151,"lastUpdatePostDateStruct":152,"startDateStruct":154,"completionDateStruct":156,"leadSponsor":158,"locationsCount":4},"100567587","this-observational-study-which-is-being-implemented-by-obtaining-statistical-data-from-a-google-form-filled-out-by-students-of-ukrainian-higher-education-institutions-aims-to-investigate-the-epidemiological-features-of-neck-pain-and-possible-risk-factors-100567587","NCT06670131","This Observational Study, Which is Being Implemented by Obtaining Statistical Data From a Google-form Filled Out by Students of Ukrainian Higher Education Institutions, Aims to Investigate the Epidemiological Features of Neck Pain and Possible Risk Factors","Neck Pain in Ukrainian Higher Education Students: Epidemiology and Risk Factors","Inclusion Criteria:\n\n\\-\n\nExclusion Criteria:\n\n* the presence of injuries, inflammatory and hereditary diseases of the spine\n* inadequate answers to open questions:\n* sleep duration more than 24 hours\n* sleep duration less than 1 hour\n* duration of stay with head tilted forward during the day more than 24 hours\n* height less than 100 cm and more than 220 cm;\n* weight less than 40 kg and more than 150 kg;\n* identical answers to all questions of the questionnaire - all A, all B, etc.","17 Years","45 Years",{"count":144,"type":21},441,"15 Months","The study aims to analyze the epidemiological, demographic, social, behavioural and neuropsychological factors of neck pain in students of higher medical education institutions in Ukraine.\n\nTo achieve the aim of this study, we will conduct an anonymous survey among medical students seeking master's degrees in Ukrainian higher education institutions.\n\nThe questionnaire will be distributed among the student community in special chats and groups in messengers.",[29,60],[31,149,150],"students","risk factors","2024-11-01",{"date":153,"type":38},"2024-11-04",{"date":155,"type":21},"2024-12-01",{"date":157,"type":21},"2026-02-01",{"name":159,"class":45},"Ukrainian Medical Stomatological Academy"]