[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"mechanical-neck-pain\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:mechanical-neck-pain":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,12,0,[8,45,65,87,109,135,157,182,207,233,257,279],{"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":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100648486","tens-versus-ultrasound-with-exercise-for-mechanical-neck-pain-100648486",false,"NCT07723586","TENS Versus Ultrasound With Exercise for Mechanical Neck Pain.","Therapeutic Benefit of Two Modalities TENS and Ultrasound Along With Exercises in the Management of Mechanical Neck Pain; A Randomized Clinical Trial","Inclusion Criteria:\n\n* Diagnosed and referred patients with mechanical neck pain.\n* Participants with subacute or chronic neck pain.\n* Participants willing to participate in the study.\n* Participants with a Visual Analog Scale (VAS) pain score greater than 5 (moderate to severe pain).\n\nExclusion Criteria:\n\n* Participants with other musculoskeletal disorders, including rheumatoid arthritis, cervical spondylosis, spondylolisthesis, cervical radiculopathy, malignancy, or neurological disorders.\n* Participants with a history of trauma or whiplash injury.\n* Participants with chronic pain conditions such as fibromyalgia.\n* Participants with vertigo or dizziness.","ALL","18 Years","45 Years",{"count":20,"type":21},44,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized clinical trial aims to compare the effectiveness of Transcutaneous Electrical Nerve Stimulation (TENS) and therapeutic ultrasound, both combined with therapeutic exercises, in the management of mechanical neck pain.\n\nA total of 44 participants male and female both with mechanical neck pain will be randomly allocated into two equal groups at the physiotherapy OPD of DOW Institute of Physical Medicine \\& Rehabilitation, Dow University of Health Sciences, Karachi. Group A will receive TENS with exercise, while group B will receive ultrasound with the same exercise protocol.\n\nBoth groups will receive 9 treatment sessions over 2 weeks. Outcomes will include pain intensity, functional disability, and cervical range of motion, assessed before and after the intervention.",[27],"Mechanical Neck Pain",[27,29,30,31],"TENS","Therapeutic Ultrasound","Algometer","RECRUITING","2026-07-21",{"date":35,"type":36},"2026-07-23","ACTUAL",{"date":38,"type":21},"2026-08-15",{"date":40,"type":21},"2026-09-15",{"name":42,"class":43},"Dow University of Health Sciences","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":63,"locationsCount":44},"100648569","effects-of-thoracic-spine-and-cervical-spine-mobilization-on-pain-functional-disability-and-quality-of-life-in-patients-with-mechanical-neck-pain-100648569","NCT07723001","Effects of Thoracic Spine and Cervical Spine Mobilization on Pain, Functional Disability, and Quality of Life in Patients With Mechanical Neck Pain.","Inclusion Criteria:\n\nParticipants of both genders aged between 20 and 40 years with a clinical diagnosis of mechanical neck pain will be included in the study. Eligible participants must have a history of neck pain lasting more than 4 weeks (subacute to chronic) and demonstrate mild to moderate functional disability, defined by a Neck Disability Index (NDI) score between 10% and 50%.\n\nExclusion Criteria:\n\nParticipants will be excluded if they present with signs or symptoms of cervical radiculopathy or myelopathy, such as a positive Spurling's test accompanied by neurological deficits, dermatomal numbness, or myotome weakness. Individuals with a history of cervical spine fracture, dislocation, or spinal surgery, as well as those with inflammatory, infectious, or neoplastic spinal conditions, will also be excluded. Additional exclusion criteria include diagnosed osteoporosis or prolonged use of systemic corticosteroids, severe cervical spine instability or vertebrobasilar insufficiency, recent trauma to the cervical or thoracic spine within the past 6 months, presence of systemic neurological disorders, pregnancy, and current participation in another physiotherapy or clinical trial for neck pain.","20 Years","40 Years",{"count":54,"type":21},66,[24],"Mechanical neck pain (MNP) is characterized as neck discomfort mostly originating from musculoskeletal components such as cervical facet joints, intervertebral discs, ligaments, and musculature, in the absence of indications of nerve root compression or severe pathological conditions. Although recent evidence supports the use of both cervical and thoracic mobilization for mechanical neck pain, there remains limited comparative research examining their combined or relative effects on pain, functional disability, and quality of life. A total of 66 Participants with mechanical neck pain (\\> 4 weeks) will be randomly allocated into two groups: Group A (Cervical spine Maitland mobilization group) will receive cervical spine Maitland mobilization throughout the 8-week intervention period, with sessions conducted twice weekly from pre-treatment to post-treatment assessment, Each session will be lasted approximately 30 minutes, consisting of manual therapy followed by standardized therapeutic exercises, supervised exercises will be performed for approximately 15 minutes. Additionally, participants in both groups will be prescribed a daily home exercise program lasting 10-15 minutes. Group B (Thoracic Plus Cervical Spine Maitland Mobilization) will receive combined thoracic and cervical spine Maitland mobilization, Thoracic mobilization will be applied to the upper thoracic segments (T1-T4) using central PA Technique. Grades III and IV mobilizations for thoracic stiffness and restore extension mobility, while lower grades will be applied in cases of increased pain sensitivity. Thoracic mobilization will be delivered for approximately 6-8 minutes, after that cervical mobilization with same protocol of supervised exercise and home pan for mechanical neck pain will be used. Each treatment session will be lasted approximately 30 minutes. Outcome measures will include: Pain intensity assessed using the Visual Analogue Scale (VAS) Functional disability will be evaluated using the Neck Disability Index (NDI), Health-related quality of life will be measured using the Short Form-36 (SF-36). The primary objective of this study is to evaluate the effects of cervical spine mobilization and thoracic spine mobilization on pain intensity, functional disability, and quality of life in patients with mechanical neck pain.",[27],"2026-07-20",{"date":35,"type":36},{"date":61,"type":36},"2026-05-01",{"date":40,"type":21},{"name":64,"class":43},"Lahore University of Biological and Applied Sciences",{"id":66,"slug":67,"hasResults":11,"nctId":68,"briefTitle":69,"officialTitle":69,"acronym":4,"eligibilityCriteria":70,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":71,"targetDuration":4,"studyType":22,"phases":73,"briefSummary":74,"conditions":75,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":44},"100647678","comparative-impact-of-integrated-neuromuscular-inhibition-technique-dry-cupping-and-dry-needling-on-mechanical-neck-pain-a-randomized-controlled-trial-100647678","NCT07711041","Comparative Impact of Integrated Neuromuscular Inhibition Technique, Dry Cupping and Dry Needling on Mechanical Neck Pain; A Randomized Controlled Trial","Inclusion Criteria:\n\n* Medically competent men and women will be included They had chronic MTrPs in the upper trapezius for more than 6 months Diagnostic criteria of being a tight band with a palpable nodule and distant pain when subjected to pressure\n\nExclusion Criteria:\n\n* subjects with previous neck or shoulder pathology (e.g., fracture, sur¬gery, inflammatory and infectious diseases), cervical disc pathology, systemic disorder, fibromyalgia, those who underwent physical therapy for at least the previous 3 months",{"count":72,"type":21},80,[24],"This study ill include four treatment groups. Group A who will receive traditional physical therapy, group B who will receive INIT plus traditional physical therapy , group C who will receive dry cupping therapy plus traditional physical therapy or group D will receive Dry needling therapy plus traditional physical therapy . All groups completed 4 weeks of intervention.",[27,76,77],"Dry Needling Technique","Dry Cupping Technique","2026-07-14",{"date":80,"type":36},"2026-07-17",{"date":82,"type":21},"2026-07",{"date":84,"type":21},"2027-05",{"name":86,"class":43},"Beni-Suef University",{"id":88,"slug":89,"hasResults":11,"nctId":90,"briefTitle":91,"officialTitle":91,"acronym":4,"eligibilityCriteria":92,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":93,"enrollmentInfo":94,"targetDuration":4,"studyType":22,"phases":96,"briefSummary":97,"conditions":98,"keywords":4,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":44},"100645798","impact-of-adding-integrated-neuromuscular-inhibition-technique-to-cervical-stabilization-exercise-in-chronic-mechanical-neck-pain-100645798","NCT07699458","Impact of Adding Integrated Neuromuscular Inhibition Technique to Cervical Stabilization Exercise in Chronic Mechanical Neck Pain","Inclusion Criteria:\n\n1. Age from 18-44 year\n2. Their body mass index will be ranging from (18-25) Kg\u002Fm2\n3. All patient has active cervical trigger point of the upper fiber of the Trapezius detected by pincer palpation\n4. Subjects must have characteristics of trigger points hardened, thickened taut bands in MPS patients.\n\nExclusion Criteria:\n\n1. Individuals with a recent history of neck or back surgery.\n2. Individuals with recent history of trauma or fracture.\n3. Individuals with congenital and pathological disorders of the cervical spine.\n4. Individuals with any psychiatric diseases","44 Years",{"count":95,"type":21},63,[24],"the goal of this clinical trial is to study the Impact of adding integrated neuromuscular inhibition technique to cervical stabilization exercise in chronic mechanical neck pain",[27],"NOT_YET_RECRUITING","2026-07-07",{"date":102,"type":36},"2026-07-13",{"date":104,"type":21},"2026-08-25",{"date":106,"type":21},"2027-01-25",{"name":108,"class":43},"Cairo University",{"id":110,"slug":111,"hasResults":11,"nctId":112,"briefTitle":113,"officialTitle":114,"acronym":4,"eligibilityCriteria":115,"healthyVolunteers":11,"sex":16,"minAge":116,"maxAge":117,"enrollmentInfo":118,"targetDuration":4,"studyType":22,"phases":119,"briefSummary":120,"conditions":121,"keywords":122,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":129,"completionDateStruct":131,"leadSponsor":133,"locationsCount":4},"100627824","eye-exercises-and-self-cervical-mobilization-in-office-workers-with-neck-pain-100627824","NCT07453654","Eye Exercises and Self-Cervical Mobilization in Office Workers With Neck Pain","Effects of Eye Exercises and Self-Cervical Mobilization on Pain, Cervical Proprioception, and Quality of Life in Office Workers With Neck Pain: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Office workers aged 25-50 years.\n* Desk-based work for ≥6 months.\n* Computer use ≥4 hours\u002Fday, ≥5 days\u002Fweek.\n* Mechanical neck pain (recurrent in the last 3 months or chronic ≥4 weeks).\n\nExclusion Criteria:\n\n* History of cervical fracture\u002Ftrauma or cervical surgery.\n* Neurological deficit (e.g., radiculopathy\u002Fmyelopathy) or vestibular disorder.\n* Cervical disc herniation, fibromyalgia, or rheumatologic disease.\n* Significant visual disorder\u002Fstrabismus or conditions affecting oculomotor\u002Fvestibulo-ocular function.\n* Participation in a neck\u002Feye exercise program within the last 6 months.\n* Regular use of analgesics or muscle relaxants.\n* Pregnancy.\n* Hemophilia or bleeding\u002Fcoagulation disorders.","25 Years","50 Years",{"count":54,"type":21},[24],"This randomized controlled trial will evaluate the effects of eye exercises and eye exercises plus self-cervical mobilization versus ergonomic education in office workers with mechanical neck pain. A total of 66 participants will be randomized to one of three groups and followed for 6 weeks. Outcomes assessed at baseline and week 6 include pain (VAS), cervical proprioception (joint position error), neck disability (NDI), cervical range of motion, and quality of life (Nottingham Health Profile).",[27],[123,124,125],"Mechanical neck pain","Office workers","Eye exercises","2026-03-12",{"date":128,"type":36},"2026-03-16",{"date":130,"type":21},"2026-03-20",{"date":132,"type":21},"2026-10-20",{"name":134,"class":43},"Bahçeşehir University",{"id":136,"slug":137,"hasResults":11,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":4,"eligibilityCriteria":70,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":141,"targetDuration":4,"studyType":22,"phases":143,"briefSummary":144,"conditions":145,"keywords":146,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":149,"lastUpdatePostDateStruct":150,"startDateStruct":152,"completionDateStruct":154,"leadSponsor":156,"locationsCount":44},"100595068","the-synergistic-effects-of-integrated-neuromuscular-inhibition-technique-and-dry-cupping-therapy-on-pain-modulation-and-functional-recovery-on-myofascial-trigger-points-of-upper-trapezius-100595068","NCT07027644","The Synergistic Effects of Integrated Neuromuscular Inhibition Technique and Dry Cupping Therapy on Pain Modulation and Functional Recovery on Myofascial Trigger Points of Upper Trapezius","The Synergistic Effects of Integrated Neuromuscular Inhibition Technique and Dry Cupping Therapy on Pain Modulation and Functional Recovery on Myofascial Trigger Points of Upper Trapezius: A Randomized Controlled Trial",{"count":142,"type":21},130,[24],"The purpose of the study is to investigate the Synergistic Effects of the Integrated Neuromuscular Inhibition Technique and Dry Cupping Therapy on Pain Modulation and functional recovery on Myofascial Trigger Points of the upper trapezius",[27],[147,148],"Dry cupping","Integrated Neuromuscular Inhibition technique","2025-08-06",{"date":151,"type":36},"2025-08-07",{"date":153,"type":36},"2025-06-20",{"date":155,"type":21},"2025-09-20",{"name":86,"class":43},{"id":158,"slug":159,"hasResults":11,"nctId":160,"briefTitle":161,"officialTitle":162,"acronym":4,"eligibilityCriteria":163,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":52,"enrollmentInfo":164,"targetDuration":4,"studyType":22,"phases":166,"briefSummary":167,"conditions":168,"keywords":169,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":173,"lastUpdatePostDateStruct":174,"startDateStruct":176,"completionDateStruct":178,"leadSponsor":180,"locationsCount":44},"100596065","deep-cervical-flexor-and-sensorimotor-training-for-chronic-neck-pain-100596065","NCT07040605","Deep Cervical Flexor and Sensorimotor Training for Chronic Neck Pain","Effect of Deep Cervical Flexor Muscle Training and Sensorimotor Training in Patient With Chronic Mechanical Neck Pain","Inclusion Criteria:\n\n* Participants aged between 20-40 years.\n* participant having neck pain report more than 4 in NPRS, and at least within the last three months known as chronic pain.\n* participant with CVA more than 45 degrees and less than 50.\n* Participant with poor cervical muscle endurance.\n\nExclusion Criteria:\n\n* Participant with acute neck pain (less than three month).\n* Participant with radiated neck pain.\n* Participant who undergone recent surgeries within the thoracic, shoulder girdle, and cervical spine regions.\n* Participants who were already undergoing treatment for neck pain.\n* Participant with fixed spinal deformity.\n* Pregnant women.",{"count":165,"type":21},60,[24],"This randomized controlled trial aims to investigate the effectiveness of deep cervical flexor muscle training combined with sensorimotor (proprioception) training in patients with chronic mechanical neck pain. The study will be conducted in outpatient clinic of the faculty of physical therapy- Cairo University, involving 60 participants aged 20-40 years with neck pain persisting for more than three months. Participants will be randomly allocated into an experimental group receiving conventional physical therapy plus deep flexor and sensorimotor training, and a control group receiving conventional treatment alone. Outcome measures will include pain intensity, craniovertebral angle (CVA), cervical range of motion (ROM), segmental mobility, neuromotor control, proprioception (head repositioning accuracy), and respiratory function (FEV1 and PEF). Assessments will be performed at baseline and after four weeks of intervention. The study seeks to provide evidence-based recommendations for physiotherapy management of mechanical neck pain, particularly addressing the gaps in literature within the regional context.",[27],[170,171,172],"mechanical neck pain","sensorimotor training","Deep cervical flexors muscles","2025-06-26",{"date":175,"type":36},"2025-06-29",{"date":177,"type":36},"2025-06-19",{"date":179,"type":21},"2025-12",{"name":181,"class":43},"Al-Neelain University",{"id":183,"slug":184,"hasResults":11,"nctId":185,"briefTitle":186,"officialTitle":187,"acronym":4,"eligibilityCriteria":188,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":18,"enrollmentInfo":189,"targetDuration":4,"studyType":22,"phases":191,"briefSummary":192,"conditions":193,"keywords":194,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":198,"lastUpdatePostDateStruct":199,"startDateStruct":201,"completionDateStruct":203,"leadSponsor":205,"locationsCount":44},"100562090","comparison-of-sustained-natural-apophyseal-glide-amp-instrument-assisted-soft-tissue-mobilization-100562090","NCT06598644","Comparison of Sustained Natural Apophyseal Glide &Amp; Instrument Assisted Soft Tissue Mobilization","Comparison of Cervical Sustained Natural Apophyseal Glide and Instrument Assisted Soft Tissue Mobilization on Mechanical Neck Pain","Inclusion Criteria:\n\n* • Both genders (males and females)\n\n  * Age between 20 and 45 years\n  * History of neck pain \\>3 month, with tenderness on palpation present on sternocleidomastoid and Levator scapulae muscles and pain aggravated by activities involving turning head towards the side\n  * Patients with pain on NPRS (at least 3)\n\nExclusion Criteria:\n\n* • patients with recent injuries or surgeries in and around the neck region\n\n  * Cervical nerve root lesion (radiculopathy)\n  * Traumatic injuries like whiplash injury\n  * malignancy in and around the neck region\n  * rheumatoid arthritis\n  * pregnant females\n  * cervicogenic headache\n  * Patients with unwillingness or inability to provide informed consent\n  * Current participation in another neck pain treatment program",{"count":190,"type":21},56,[24],"The aim of this randomized controlled trial is to evaluate and compare the effectiveness of two therapeutic techniques-Cervical Sustained Natural Apophyseal Glide (SNAG) and Instrument-Assisted Soft Tissue Mobilization (IASTM)-in the treatment of mechanical neck pain. The trial seeks to determine which method is more effective in reducing pain, improving range of motion, and enhancing overall neck function in individuals suffering from mechanical neck pain.",[27],[195,196,197],"cervical SNAGS","Instrument assisted soft tissue mobilization","ergon technique","2025-02-20",{"date":200,"type":36},"2025-02-21",{"date":202,"type":36},"2024-09-20",{"date":204,"type":21},"2025-12-26",{"name":206,"class":43},"Riphah International University",{"id":208,"slug":209,"hasResults":11,"nctId":210,"briefTitle":211,"officialTitle":212,"acronym":4,"eligibilityCriteria":213,"healthyVolunteers":214,"sex":16,"minAge":51,"maxAge":117,"enrollmentInfo":215,"targetDuration":4,"studyType":22,"phases":217,"briefSummary":218,"conditions":219,"keywords":220,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":225,"lastUpdatePostDateStruct":226,"startDateStruct":228,"completionDateStruct":230,"leadSponsor":232,"locationsCount":44},"100573740","effect-of-met-with-and-without-mcte-in-mechanical-neck-pain-100573740","NCT06750211","Effect of MET With and Without MCTE in Mechanical Neck Pain","Effects of Muscle Energy Techniques With and Without Motor Control Therapeutic Exercises on Pain, Range of Motion and Disability in Patients With Mechanical Neck Pain.","Inclusion Criteria:\n\n* • Subjects were between 20 and 50 years old.\n\n  * Pain in cervical or neck region with no radiating pain in one or both upper limbs.\n  * Pain minimum of 3 months.\n  * Neck disability index (NDI) score of should be at least 10%.\n  * Forward head posture.\n\nExclusion Criteria:\n\n* • Neck pain associated with vertigo.\n\n  * Irradiated neck pain.\n  * Vertebral fracture.\n  * Osteoporosis.\n  * Previous neck injury.\n  * Red flags (night pain, severe muscle loss, loss of involuntary control.\n  * Subjects with difficulty in communication or understanding.",true,{"count":216,"type":21},50,[24],"Work had to be done previously on METs and MCTE techniques, but no study has compared both techniques together to make it more comprehensible. The rationale of this will be to find out the combined effect of motor control therapeutic exercises and muscle energy technique for the treatment of pain, range of motion and disability associated with mechanical neck pain. This study will be effective for the clinicians to treat patients of mechanical neck pain.",[27],[221,222,223,224],"Neck pain","Range of motion","Muscle energy technique","Motor control therapeutic exercise","2024-12-20",{"date":227,"type":36},"2024-12-27",{"date":229,"type":36},"2024-07-04",{"date":231,"type":21},"2025-01-08",{"name":206,"class":43},{"id":234,"slug":235,"hasResults":11,"nctId":236,"briefTitle":237,"officialTitle":237,"acronym":238,"eligibilityCriteria":239,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":240,"enrollmentInfo":241,"targetDuration":4,"studyType":22,"phases":242,"briefSummary":243,"conditions":244,"keywords":245,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":249,"lastUpdatePostDateStruct":250,"startDateStruct":252,"completionDateStruct":254,"leadSponsor":256,"locationsCount":4},"100571427","sustained-natural-apophysial-glide-versus-instrument-assisted-soft-tissue-mobilization-in-patients-with-chronic-mechanical-neck-pain-100571427","NCT06720116","Sustained Natural Apophysial Glide Versus Instrument Assisted Soft Tissue Mobilization in Patients With Chronic Mechanical Neck Pain","MNP","Inclusion Criteria:\n\n* Sixety patients of chronic mechanical neck pain diagnosed and reffered from physicians will be participants in the study .\n* Patients of both genders will be included.\n* The age of the participants will beranged from 20 and 55 years\n* The BMI ranged between 18.9 and 25 kg\u002Fm2\n* All patients who suffered from neck pain more than 3 months.\n\nExclusion Criteria:\n\n* Malignancy\n* cervical and cranial surgery\n* Recent fractures\n* spinal tumors\n* severe disc herniation\n* uncontrolled hypertension\n* Heart Disease ( arrhythmia, pacemaker).\n* Pregnant and breast feeding women.","55 Years",{"count":165,"type":21},[24],"this study will be conducted to investigate the effect of sustained natural apophysial glide and Instrument assisted soft tissue mobilization on pain intensity, cervical range of motion and neck functional disability level in patients with chronic mechanical neck pain",[27],[246,247,248],"Sustained Natural Apophysial Glide","instrument Assisted Soft Tissue Mobilization","Chronic Mechanical Neck Pain","2024-12-03",{"date":251,"type":36},"2024-12-06",{"date":253,"type":21},"2024-12-10",{"date":255,"type":21},"2025-03-30",{"name":108,"class":43},{"id":258,"slug":259,"hasResults":11,"nctId":260,"briefTitle":261,"officialTitle":262,"acronym":4,"eligibilityCriteria":263,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":264,"enrollmentInfo":265,"targetDuration":4,"studyType":22,"phases":266,"briefSummary":267,"conditions":268,"keywords":269,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":271,"lastUpdatePostDateStruct":272,"startDateStruct":274,"completionDateStruct":276,"leadSponsor":278,"locationsCount":44},"100558872","comparison-of-gongs-and-kaltenborn-mobilization-on-neck-pain-100558872","NCT06556771","Comparison of Gongs and Kaltenborn Mobilization on Neck Pain","Comparison of Gongs Mobilization and Kaltenborn Mobilization on Mechanical Neck Pain","Inclusion Criteria:\n\nParticipants falling in this category would be recruited into the study.\n\n* • Age 18 -65 years\n\n  * Both male and female\n  * Primary complaint of neck pain with or without radiating to Upper extremity\n  * Pain confined to posterior aspect of neck with mechanical characteristics such as symptoms provoked by neck movement, by palpation of cervical muscles and by sustained posture.\n  * Subjects who are willing to participate in study.\n  * Patients with Mechanical neck pain\n\nExclusion Criteria:\n\n* Participants falling in this category would be excluded from the study.\n\n  * Bilateral upper extremity symptoms\n  * Whiplash injury\n  * Trauma or tumor around neck\n  * Previous neck surgery\n  * Spinal infection\n  * Cervical radiculopathy and myelopathy\n  * Vascular syndromes","65 Years",{"count":20,"type":21},[24],"The aim of this randomized controlled trial is to find the effect of Gongs mobilization in comparison with Kaltenborn mobilization on mechanical neck pain , range of motion and proprioception.A randomized control trial that will include total 44 participants. The first group will receive Gongs mobilization along with conventional therapy and 2nd group will receive Kaltenborn mobilization along with conventional therapy.",[27],[270],"Gongs mobilization, Kaltenborn mobilization , Mechanical neck pain , proprioception","2024-08-13",{"date":273,"type":36},"2024-08-16",{"date":275,"type":36},"2024-08-09",{"date":277,"type":21},"2025-01-10",{"name":206,"class":43},{"id":280,"slug":281,"hasResults":11,"nctId":282,"briefTitle":283,"officialTitle":284,"acronym":4,"eligibilityCriteria":285,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":286,"targetDuration":4,"studyType":22,"phases":288,"briefSummary":289,"conditions":290,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":291,"lastUpdatePostDateStruct":292,"startDateStruct":294,"completionDateStruct":296,"leadSponsor":298,"locationsCount":300},"100518517","effect-of-dynamic-cupping-versus-myofascial-release-therapy-in-patients-with-mechanical-neck-pain-100518517","NCT06031571","Effect of Dynamic Cupping Versus Myofascial Release Therapy in Patients With Mechanical Neck Pain","Effect of Dry Cupping Massage Versus Myofascial Release Therapy in Patients With Mechanical Non-specific Neck Pain: a Quasi-experimental Study","Inclusion Criteria:\n\n1. Age between 18- 40 years.\n2. Participants have experienced mechanical neck pain for at least the previous 3 months.\n\nExclusion Criteria:\n\n* Participants aged below 18 years-old and those above 40 years old\n* Mechanical neck pain due to trauma, disc protrusion, congenital deformity of the spine, spinal stenosis, and rheumatoid disease.",{"count":287,"type":21},38,[24],"A Quasi-experimental study will investigate the effect of dry cupping massage versus myofascial release on patients with mechanical neck pain.",[27],"2024-06-23",{"date":293,"type":36},"2024-06-25",{"date":295,"type":36},"2023-08-01",{"date":297,"type":21},"2024-07-20",{"name":299,"class":43},"South Valley University",2]