[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"shoulder-impingement-syndrome\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:shoulder-impingement-syndrome":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,52,81,112,136,162,188,207,239,256,278],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":4,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":51},"100610542","the-role-of-pectoralis-minor-tightness-in-the-development-of-rotator-cuff-tears-100610542",false,"NCT07228936","The Role of Pectoralis Minor Tightness in the Development of Rotator Cuff Tears","The Role of Pectoralis Minor Muscle Tightness in the Development of Rotator Cuff Tears: A Propensity Score Matched Case-Control Study","PMinor-Rotator","Inclusion criteria consisted of patients aged 18-55 years who were scheduled to undergo surgical treatment for a partial-thickness rotator cuff tear (case group) and individuals aged 18-55 years with no evidence of rotator cuff or other shoulder pathology on magnetic resonance imaging (control group). Patients were excluded if they had a history of trauma, thoracic outlet syndrome, systemic inflammatory disease, prior surgery on the affected shoulder, and declined participation in the examination.",true,"ALL","18 Years","55 Years",{"count":22,"type":23},90,"ESTIMATED","OBSERVATIONAL","This study investigates whether tightness of a small chest muscle called the pectoralis minor is associated with the development of partial rotator cuff tears in the shoulder. Using a propensity score matched case-control design, the study compares patients with rotator cuff tears (case group, n=45) to patients with intact rotator cuffs (control group, n=45).\n\nAdults aged 18-55 with shoulder pain who are evaluated by MRI and\u002For shoulder arthroscopy at Gazi University Hospital may be invited. The case group includes patients found to have partial rotator cuff tears during arthroscopy. The control group includes patients whose rotator cuff was documented as intact by MRI. Groups are matched 1:1 on age, sex, BMI, and dominant side.\n\nBefore surgery, two trained clinician measures shoulder posture and pectoralis minor length using simple external tools (a digital caliper and ruler-like square). For arthroscopy patients, the surgeon records general arthroscopic findings. No extra procedures are added for research.\n\nWe expect to include 90 participants total. The primary hypothesis is that pectoralis minor tightness is more prevalent in patients with rotator cuff tears compared to controls. A secondary hypothesis is that tears in patients with pectoralis minor tightness more often partial-thickness bursal side rotator cuff tear. Results may help clinicians understand shoulder mechanics and improve prevention or rehabilitation strategies.",[27,28,29,30],"Shoulder Impingement Syndrome","Rotator Cuff Injuries","Pectoralis Minor Tightness","Pectoralis Minor Muscle Tension",[32,28,33,34,35,36,37,38],"rotator cuff","Posture","Scapula","Pectoralis Muscles","Arthroscopy","Shoulder Joint","Pectoralis Minor","RECRUITING","2026-06-20",{"date":42,"type":43},"2026-06-25","ACTUAL",{"date":45,"type":43},"2025-03-18",{"date":47,"type":23},"2026-06-30",{"name":49,"class":50},"Gazi University","OTHER",1,{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":17,"sex":18,"minAge":58,"maxAge":59,"enrollmentInfo":60,"targetDuration":4,"studyType":62,"phases":63,"briefSummary":65,"conditions":66,"keywords":68,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":51},"100640584","prone-row-exercise-versus-lateral-pull-down-exercise-in-shoulder-impingement-syndrome-with-scapular-dyskinesia-100640584","NCT07577791","Prone Row Exercise Versus Lateral Pull Down Exercise In Shoulder Impingement Syndrome With Scapular Dyskinesia","Inclusion Criteria:\n\n* -Fifty-four male and female.\n* Individuals diagnosed with SIS and aged between 40-65 years with right-hand dominance (Andrea et al., 2024).\n* Participants experiencing shoulder pain persisting for a minimum duration of 3 months (Lucas et al., 2022).\n* Subjects with a primary complaint of shoulder impingement and scapular dyskinesia according to Neer's classification specifically in stages I and II are referred by an orthopedist (El Melhat et al., 2025).\n* Body mass index (BMI) is ≥ 25 kg\u002Fm² (Maryam et al., 2023).\n* Individuals with a positive Lateral Scapular Slide Test (LSST), defined as a side-to-side scapular difference of 1.5 cm or more in any of the three arm positions, indicating scapular asymmetry associated with dyskinesis (Kibler, 2003; Odom, 2001).\n* All participants must have the cognitive ability to understand instructions and provide informed consent, consistent with standards highlighted in recent informed consent meta-analyses (Tam et al., 2015).\n\nExclusion Criteria:\n\n* History of shoulder surgery, dislocation, or fracture (Crawshaw et al., 2010).\n* History of neurological disorders (Crawshaw et al., 2010).\n* Participants will be excluded if they had cervical spine pain or any signs of cervical radiculopathy (Magee, 2014).\n* Individuals with chronic low back pain will be also excluded (Mohamed et al., 2022).\n* Pregnant women will be excluded from participation in this study.","40 Years","65 Years",{"count":61,"type":23},54,"INTERVENTIONAL",[64],"NA","The purpose of this study is to compare the prone row exercise, and the lateral pull down exercise, in individuals diagnosed with shoulder impingement syndrome and scapular dyskinesia regarding latissimus dorsi strength, middle trapezius strength, lower trapezius strength, rhomboids strength, Visual analog scale score, Shoulder pain and disability index score and scapular stability test values.",[27,67],"Scapular Dyskinesis",[69,70],"shoulder impingement syndrome","scapular dyskinesia","NOT_YET_RECRUITING","2026-05-09",{"date":74,"type":43},"2026-05-13",{"date":76,"type":23},"2026-08-29",{"date":78,"type":23},"2026-09-30",{"name":80,"class":50},"Cairo University",{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":4,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":18,"minAge":88,"maxAge":59,"enrollmentInfo":89,"targetDuration":4,"studyType":62,"phases":91,"briefSummary":92,"conditions":93,"keywords":97,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":51},"100615288","graded-motor-imagery-and-task-oriented-exercise-in-shoulder-impingement-100615288","NCT07290660","Graded Motor Imagery and Task-Oriented Exercise in Shoulder Impingement","Effectiveness of Graded Motor Imagery and Task-Oriented Exercise Training in Shoulder Impingement Syndrome","Inclusion Criteria:Adults aged 25-65 years\n\nDiagnosed with Stage I or Stage II shoulder impingement syndrome by an Orthopedics or Physical Medicine and Rehabilitation physician\n\nPositive Neer and Hawkins tests\n\nUnilateral shoulder pain for at least 3 months\n\nNo participation in any physiotherapy program for shoulder problems within the last year\n\nAbility to cooperate and follow instructions\n\nA score of 24 or above on the Standardized Mini-Mental Test -\n\nExclusion Criteria:\n\nHistory of previous shoulder surgery\n\nLocal corticosteroid injection within the last three months\n\nPresence of uncontrolled neurological, cardiac, or systemic diseases that may interfere with function\n\nCognitive impairments that may affect proper understanding or execution of the motor imagery program\n\nA score below 24 on the Standardized Mini-Mental Test\n\n\\-","25 Years",{"count":90,"type":23},66,[64],"This study aims to compare the effects of graded motor imagery and task-oriented exercise training in individuals with shoulder impingement syndrome. A total of 66 participants aged 25-65 years will be randomly assigned to one of three groups: conventional physiotherapy, graded motor imagery, or task-oriented exercise training. All groups will receive standardized electrotherapy, while the intervention groups will additionally complete 6-week graded motor imagery or task-oriented exercise programs.\n\nPrimary outcomes include pain intensity, shoulder range of motion, muscle strength, proprioception, functional status, kinesiophobia, laterality recognition, movement imagery ability, and patient satisfaction. Assessments will be conducted before and after the intervention by the same physiotherapist. The study aims to determine whether motor imagery-based or task-oriented rehabilitation provides additional benefits compared with conventional physiotherapy in individuals with shoulder impingement syndrome.",[27,94,95,96],"Pain","Motor Imagery Training","Task Oriented Training",[98,99,100,101,102],"Shoulder impingement syndrome","Graded motor imagery","Task-oriented exercise","Rehabilitation","pain","2025-12-05",{"date":105,"type":43},"2025-12-18",{"date":107,"type":43},"2025-12-01",{"date":109,"type":23},"2026-12-30",{"name":111,"class":50},"Fenerbahce University",{"id":113,"slug":114,"hasResults":11,"nctId":115,"briefTitle":116,"officialTitle":116,"acronym":4,"eligibilityCriteria":117,"healthyVolunteers":11,"sex":18,"minAge":88,"maxAge":58,"enrollmentInfo":118,"targetDuration":4,"studyType":62,"phases":120,"briefSummary":121,"conditions":122,"keywords":123,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":4},"100611223","impact-of-core-stability-training-on-function-in-patient-with-shoulder-impingement-syndrome-among-manual-operated-hand-workers-100611223","NCT07237789","Impact of Core Stability Training on Function in Patient With Shoulder Impingement Syndrome Among Manual Operated Hand Workers","Inclusion Criteria:\n\nmanually operated hand workers (males and females), Age from 25-to\n\n-40 years, Shoulder impingement syndrome, and with No previous history of shoulder surgery that may affect their performance.\n\nExclusion Criteria:\n\nPatient who has a history of shoulder instability, History of shoulder dislocation, Patient who has current symptoms related to the cervical spine, Patient who has a history of acromioclavicular pain, and Low back pain (LBP) will be excluded.",{"count":119,"type":23},40,[64],"Even at the early stage of employment exposure to mechanical factors such as lifting heavy weights, working with hands at or above shoulder level, and pushing or pulling heavy loads are independent risk factors for new-onset shoulder pain . Shoulder-related problems among workers doing spading are 53.1% and 57.7% among workers brick carrying tasks, these shoulder issues may be the result of repetitive awkward movement (beyond ninety degree raising with abduction position) of the shoulder during these activities .",[27],[124,125,126,127],"Core Stability","Function","Hand Worker","Shoulder Impingement","2025-11-18",{"date":130,"type":43},"2025-11-20",{"date":132,"type":23},"2025-12",{"date":134,"type":23},"2026-02",{"name":80,"class":50},{"id":137,"slug":138,"hasResults":11,"nctId":139,"briefTitle":140,"officialTitle":141,"acronym":142,"eligibilityCriteria":143,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":144,"targetDuration":4,"studyType":62,"phases":146,"briefSummary":147,"conditions":148,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":151,"lastUpdatePostDateStruct":152,"startDateStruct":154,"completionDateStruct":156,"leadSponsor":158,"locationsCount":161},"100574488","performance-and-safety-of-lightforce-therapy-lasers-on-shoulder-soft-tissue-inflammation-pain-reduction-100574488","NCT06759935","Performance and Safety of LightForce® Therapy Lasers on Shoulder Soft Tissue Inflammation Pain Reduction","Randomized, Sham Controlled, Single Blind Study on the Performance and Safety of Photo Biomodulation Therapy (PBMT) With LightForce® Therapy Lasers on Shoulder Soft Tissue Inflammation Pain Reduction","SHINE","Inclusion Criteria:\n\n1. Patient male or female with age ≥18 years old\n2. Patient with diagnosis of shoulder soft tissue inflammation due to SAIS\u002FRCT (as confirmed by physical examination and\u002For imaging) to be treated by LightForce® Therapy Lasers according to its indications.\n3. Patient suffering from shoulder soft tissue inflammation due to SAIS\u002FRCT pain for more than 3 months prior to enrollment\n4. Pain (either persistent or during activities) score reported by the subject at baseline ≥ 40 mm measured on VAS\n5. Patient able to provide written informed consent\n\nExclusion Criteria:\n\n1. Patient with musculoskeletal pathological conditions not to be treated with\u002Fcontraindication to the use of LightForce® Therapy Lasers according to its intended use and indications\n2. Patients who are taking drugs that have heat or light sensitive contraindications, such as but not limited to certain types of steroids\n3. Patients who are administered with corticosteroids, should discontinue the treatment at least 2 weeks prior to study treatment start\n4. Pregnant females or females of childbearing potentially planning to become pregnant during the study participation\n5. Patients who had systemic inflammatory conditions (i.e.rheumatoid arthritis, polymyalgia rheumatica)\n6. Patients who underwent intra-articular injection (Ialuronic acid, platelet rich plasma or corticosteroids) in the shoulder in the last 3 months\n7. Patients who have a disease that would limit their participation in exercises (i.e. severe chronic obstructive pulmonary disease, severe heart failure, cerebrovascular event history)\n8. Patients with a prior history of surgical intervention and implantation of a metal implant into the affected shoulder\n9. Patients with a diagnosis of active cancer\n10. Patients with tattoos covering more than 30% of the area to be treated with LightForce® Therapy Lasers\n11. Patients who are mentally or physically incapacitated\n12. Patient participating in other clinical study or has completed a clinical study less than 30 days prior to enrollment\n13. Patient affected by shoulder soft tissue acute inflammation due to recent sport injury or trauma\n14. Patients with other musculoskeletal problems of the shoulder joint such as calcifying tendinitis, full thickness rotator-cuff tear, adhesive capsulitis, fibromyalgia, recent surgery or fracture of the shoulder joint, and\u002For undergoing to specific physiotherapy for these (\"recent\" is defined as within 30 days prior to enrollment).\n15. Patients with other clinically significant co-morbidities that make the patient unsuitable for study participation, at the discretion of the investigator",{"count":145,"type":23},130,[64],"DJO UK Ltd (ENOVIS) is conducting this study to assess the effectiveness of LightForce® Therapy Lasers on pain reduction in shoulder soft tissue inflammation. In detail this study will assess superiority of LightForce® Therapy Lasers combined with standard of care, represented by physiotherapy\u002Fexercise program compared to sham laser combined with standard of care (physiotherapy\u002Fexercise program) on pain reduction in subjects with shoulder soft tissue inflammation due to Impingement (Subacromial impingement syndrome (SAIS)) or Rotator Cuff Tendinopathy (RCT),. In addition, this study allows to collect post market clinical data on the safety and performance of LightForce® Therapy Lasers, when used, following the normal clinical practice, in accordance with its approved and CE marked intended use.",[149,27,150],"Shoulder Pain","Rotator Cuff Tendinitis","2025-11-14",{"date":153,"type":43},"2025-11-17",{"date":155,"type":43},"2025-02-21",{"date":157,"type":23},"2026-12",{"name":159,"class":160},"DJO UK Ltd","INDUSTRY",10,{"id":163,"slug":164,"hasResults":11,"nctId":165,"briefTitle":166,"officialTitle":167,"acronym":4,"eligibilityCriteria":168,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":59,"enrollmentInfo":169,"targetDuration":4,"studyType":62,"phases":171,"briefSummary":172,"conditions":173,"keywords":174,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":178,"lastUpdatePostDateStruct":179,"startDateStruct":181,"completionDateStruct":183,"leadSponsor":185,"locationsCount":4},"100607608","effectiveness-of-kinesiologic-taping-and-dry-needling-in-the-treatment-of-subacromial-pain-syndrome-100607608","NCT07190768","Effectiveness of Kinesiologic Taping and Dry Needling in the Treatment of Subacromial Pain Syndrome","The Comparison of the Effectiveness of Kinesiologic Taping and Dry Needling in the Treatment of Subacromial Pain Syndrome: a Randomize Trial","Inclusion Criteria:\n\nAge 18-65 years\n\nPain in the upper, outer arm, especially during shoulder elevation\n\nShoulder pain lasting more than 6 weeks with or without partial rotator cuff tear\n\nAt least three of the following findings:\n\nPainful arc during flexion or abduction\n\nPositive Neer test\n\nPositive Hawkins-Kennedy test\n\nPainful resisted external rotation\n\nPositive Jobe's test\n\nDiagnosis confirmed by MRI evaluation when indicated\n\nExclusion Criteria:\n\nParticipation in a physical therapy program or receipt of injection therapy within the past 3 months\n\nPrevious shoulder surgery\n\nPresence of joint contracture\n\nComplete tendon rupture\n\nCervical radiculopathy\n\nSystemic inflammatory disease (e.g., rheumatoid arthritis, ankylosing spondylitis)\n\nKnown allergy to tape or materials used in interventions\n\nBleeding disorders\n\nLocal infection or open wound in the treatment area\n\nCognitive dysfunction that prevents cooperation\n\nHistory of malignancy",{"count":170,"type":23},100,[64],"This study aims to compare the effectiveness of two common physiotherapy methods, Kinesiologic Taping (KT) and Dry Needling (DN), in the treatment of Subacromial Pain Syndrome (SAPS), a frequent cause of shoulder pain. The trial also investigates whether using KT and DN together provides greater benefits than using them separately. The main goal is to determine which treatment approach is more effective in reducing pain and improving shoulder function in patients with SAPS.",[149,27],[175,176,177],"Kinesiologic taping","shoulder pain","dry needling","2025-09-23",{"date":180,"type":43},"2025-09-24",{"date":182,"type":23},"2025-10-01",{"date":184,"type":23},"2026-10-01",{"name":186,"class":187},"Bursa City Hospital","OTHER_GOV",{"id":189,"slug":190,"hasResults":11,"nctId":191,"briefTitle":192,"officialTitle":192,"acronym":193,"eligibilityCriteria":194,"healthyVolunteers":17,"sex":18,"minAge":88,"maxAge":58,"enrollmentInfo":195,"targetDuration":4,"studyType":24,"phases":4,"briefSummary":197,"conditions":198,"keywords":4,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":199,"lastUpdatePostDateStruct":200,"startDateStruct":202,"completionDateStruct":204,"leadSponsor":206,"locationsCount":51},"100576799","electromyographic-activity-of-posterior-oblique-sling-muscles-in-patients-with-shoulder-impingement-syndrome-100576799","NCT06789991","Electromyographic Activity of Posterior Oblique Sling Muscles in Patients With Shoulder Impingement Syndrome","EMG","Inclusion Criteria:\n\n1. Both male and female patients with shoulder impingement syndrome.\n2. patients complain from unilateral shoulder pain with chronic conditions of SIS ≥ 3 months.\n3. Patient age from 25 to 40 years.\n4. Patients with Positive impingement tests.\n5. Patients with painful arc of movement (60°- 120°)\n\nExclusion Criteria:\n\n1. Patients with Numbness or tingling of upper extremity.\n2. Patients with Shoulder fracture or previous shoulder surgery, and Acromioclavicular or shoulder dislocation.\n3. Patients with Any traumatic injury to the lower limb in the previous 6 months.\n4. Any spine surgery within the last 2 years.\n5. Patients with history of lower back pain in past 12 months .\n6. Patients with history of lower extremity dysfunctions in the past 12 months .\n7. Participants who had taken any drugs (e.g. statins and spasmed), which have effects on the skeletal muscles.\n8. Open wounds, rashes, psoriasis, skin irritations, or skin conditions of any kind in the region of electrode placement\n9. Participants with a Body Mass Index (BMI) ≥ 30",{"count":196,"type":23},60,"this study aims to assess the gluteus maximus muscle electromyographic activity and the latissimus dorsi muscle electromyographic activity in patients with shoulder impingement syndrome , to improve the assessment procedure and the rehabilitation program for treating patients with shoulder impingement syndrome more effectively. .",[27],"2025-01-22",{"date":201,"type":43},"2025-01-23",{"date":203,"type":23},"2025-01",{"date":205,"type":23},"2025-04",{"name":80,"class":50},{"id":208,"slug":209,"hasResults":11,"nctId":210,"briefTitle":211,"officialTitle":212,"acronym":4,"eligibilityCriteria":213,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":214,"enrollmentInfo":215,"targetDuration":4,"studyType":62,"phases":217,"briefSummary":218,"conditions":219,"keywords":224,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":230,"lastUpdatePostDateStruct":231,"startDateStruct":233,"completionDateStruct":235,"leadSponsor":237,"locationsCount":51},"100570881","the-clinical-efficacy-of-different-durations-of-suprascapular-nerve-pulsed-radiofrequency-100570881","NCT06713005","The Clinical Efficacy of Different Durations of Suprascapular Nerve Pulsed Radiofrequency","The Clinical Efficacy of Different Durations of Suprascapular Nerve Pulsed Radiofrequency Treatment in Chronic Soulder Pain","Inclusion Criteria:\n\n* Patients aged 18-80 years\n* Shoulder pain caused by impingement syndrome\n* Shoulder pain due to supraspinatus tendinosis\n* Diagnosis of impingement syndrome and supraspinatus tendinosis confirmed through physical examination and radiological imaging (MRI)\n* Pain persisting for 3 months or longer\n* Numeric Pain Rating Scale (NRS) score of 4 or higher despite conservative treatment\n\nExclusion Criteria:\n\n* Patients unwilling to participate in the study\n* Presence of chronic pain due to other conditions\n* Presence of cervical radiculopathy\n* History of opioid use\n* Uncontrolled diabetes (HbA1c \\> 8)\n* History of shoulder surgery on the affected side\n* Uncontrolled psychiatric disorders despite medical treatment\n* History of cancer\n* History of stroke","80 Years",{"count":216,"type":23},30,[64],"Chronic shoulder pain due to impingement syndrome and supraspinatus tendinosis is a debilitating condition. Suprascapular nerve innervates most part of shoulder joint. Supraspinatus nerve block can be used as a part of pain therapy. However, its efficacy is short-lasting. To prolong analgesia, short bursts of electrical stimulation to suprascapular nerve may be applied. To the date there is no consensus about duration of these type of stimulation. Investigators' aim is to investigate efficacy of two different duration of stimulation (pulsed radiofrequency) on chronic shoulder pain.",[220,27,221,222,223],"Suprascapular Nerve","Pulsed Radiofrequency","Chronic Pain","Supraspinatus Tendinopathy",[225,226,227,228,229],"pulsed radiofrequency","suprascapular nerve","chronic pain","impingement syndrome","Supraspinatus tendinopathy","2024-12-24",{"date":232,"type":43},"2024-12-27",{"date":234,"type":23},"2025-01-01",{"date":236,"type":23},"2025-07-01",{"name":238,"class":50},"Ankara University",{"id":240,"slug":241,"hasResults":11,"nctId":242,"briefTitle":243,"officialTitle":243,"acronym":4,"eligibilityCriteria":244,"healthyVolunteers":11,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":245,"targetDuration":4,"studyType":24,"phases":4,"briefSummary":246,"conditions":247,"keywords":4,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":248,"lastUpdatePostDateStruct":249,"startDateStruct":250,"completionDateStruct":252,"leadSponsor":254,"locationsCount":51},"100574077","role-of-dynamic-ultrasound-in-assessment-of-shoulder-impingement-syndrome-100574077","NCT06754592","Role of Dynamic Ultrasound in Assessment of Shoulder Impingement Syndrome","Inclusion Criteria:\n\n* male and female patients present with shoulder pain with positive clinical tests suggestive of shoulder impingement syndrome\n\nExclusion Criteria:\n\n* History of shoulder surgery, instability disorders, shoulder girdle fracture, radiation therapy to the shoulder, neoplastic lesions, and congenital anomalies of the shoulder. Patients having contraindications to perform MRI (Patients with electrically, magnetically, or mechanically activated implants, pacemakers, cochlear implants, or any metallic orthopedic implants) and claustrophobic patients).",{"count":216,"type":23},"This study aims to evaluate the effectiveness of dynamic high-resolution ultrasonography in identifying various abnormalities of the shoulder impingement syndrome, especially the subacromial type, and to determine the added value of dynamic ultrasonography compared to static examination of such cases. Furthermore, we will compare these findings to MRI, which we regard as the standard in our cases.",[27],"2024-12-23",{"date":234,"type":43},{"date":251,"type":23},"2024-12-26",{"date":253,"type":23},"2025-06-30",{"name":255,"class":50},"Sohag University",{"id":257,"slug":258,"hasResults":11,"nctId":259,"briefTitle":260,"officialTitle":261,"acronym":4,"eligibilityCriteria":262,"healthyVolunteers":11,"sex":18,"minAge":263,"maxAge":264,"enrollmentInfo":265,"targetDuration":4,"studyType":62,"phases":267,"briefSummary":268,"conditions":269,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":270,"lastUpdatePostDateStruct":271,"startDateStruct":273,"completionDateStruct":275,"leadSponsor":277,"locationsCount":51},"100531143","the-effect-of-lower-limb-kinetic-chain-exercise-in-shoulder-impingement-100531143","NCT06195956","The Effect of Lower Limb Kinetic Chain Exercise in Shoulder Impingement","Effects of Lower Limb Kinetic Chain Exercise to Shoulder Rehabilitation Program in Patients With Shoulder Impingement Syndrome","Inclusion Criteria:\n\n* Age ranges between 20 and 45 years old\n* Unilateral shoulder pain lasting more than 6 weeks\n* At least one positive finding in each of these categories:\n\n  1. Painful arc of movement during flexion or abduction\n  2. Positive Neer or Hawkins-Kennedy impingement signs\n  3. Pain on resisted lateral rotation, abduction or Jobe test\n\nExclusion Criteria:\n\n* History of surgery\n* History of fracture or dislocation\n* Type III acromion\n* Rotator cuff tear\n* Long head of biceps tendon tear\n* Cervical radiculopathy","20 Years","45 Years",{"count":266,"type":23},50,[64],"The goal of this clinical trial study is to investigate the effect of performing lower limb kinetic chain exercise on muscle activation of scapular muscle strength ratio in patients with shoulder impingement. the main question it aims to answer is:\n\nDoes the addition of lower limb kinetic chain exercise to a shoulder exercise program improve scapular muscles strength ratio in patients with shoulder impingement? participants will be devided into two groups to be compared: The first group will be given a rehabilitation program consisting of strengthening exercises (for scapular stabilizers and rotator cuff) and stretching exercises (for pectoralis major, pectoralis minor, latissimus dorsi, levator scapula) The second group will be given the same exercises in addition to lower limb kinetic chain exercise",[27],"2024-08-19",{"date":272,"type":43},"2024-08-21",{"date":274,"type":43},"2024-01-20",{"date":276,"type":23},"2024-10-01",{"name":80,"class":50},{"id":279,"slug":280,"hasResults":11,"nctId":281,"briefTitle":282,"officialTitle":283,"acronym":4,"eligibilityCriteria":284,"healthyVolunteers":11,"sex":18,"minAge":263,"maxAge":285,"enrollmentInfo":286,"targetDuration":4,"studyType":62,"phases":287,"briefSummary":288,"conditions":289,"keywords":290,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":292,"lastUpdatePostDateStruct":293,"startDateStruct":295,"completionDateStruct":297,"leadSponsor":299,"locationsCount":51},"100523198","shoulder-impingement-syndrome-and-graded-motor-imagery-100523198","NCT06092502","Shoulder Impingement Syndrome and Graded Motor Imagery","The Effectiveness of Graded Motor Imagery Therapy Applied in Addition to the Traditional Physiotherapy Program in Shoulder Impingement Syndrome","Inclusion Criteria:\n\n* 20-50 years of age with complaints of shoulder pain in the anterio-lateral region lasting more than 6 weeks, with a positive Neer impingement test and\u002For a positive Hawkins-Kennedy test\n* Additionally, patients must have at least one of the symptoms listed. These symptoms are: painful arch on active shoulder elevation, pain with resisted shoulder external rotation in abduction at 90°, and a positive empty can test.\n\nExclusion Criteria:\n\n* Having had a steroid injection into the shoulder within the last 3 months\n\n  * Previous surgery on the neck, thoracic spine or shoulder\n  * Red flags (e.g. tumor, fracture, metabolic diseases, rheumatoid arthritis, osteoporosis, resting blood pressure greater than 140\u002F90 mmHg, history of long-term steroid use)\n  * History of shoulder dislocation, subluxation, fracture, adhesive capsulitis, frozen shoulder, or cervical or thoracic surgery\n  * History of full-thickness rotator cuff tear\n  * History of cervical disc herniation in the last 6 weeks\n  * History of breast cancer on the involved side\n  * Isolated acromioclavicular joint pathology (i.e., pain directly localized over the acromioclavicular joint).\n  * Signs of cervical radiculopathy, radiculitis, or referred pain originating from the cervical spine\n  * Receiving treatment for shoulder pain in the last 3 months\n  * Being currently pregnant (Dunning, 2022)\n  * Scoring ≤24 on the Standardized Mini Mental Test was determined.","50 Years",{"count":216,"type":23},[64],"Graded motor imagery (GMI): used successfully in chronic, complex and painful clinical conditions accompanied by many pain and movement problems; It is a treatment, education and rehabilitation process that is based on recently obtained scientific data and current clinical studies, is individually adapted and approaches the individual holistically with a biopsychosocial model. Nowadays, it is frequently used in the treatment of some neurological diseases. In addition, these approaches are also used in the treatment of some orthopedic diseases including chronic pain. There are a limited number of studies in which the mentioned approaches are used together in stages, and the stages are mostly used alone. There is only one study in the literature on subacromial pain syndrome (SAS), which is the most common cause of shoulder pain and causes radiator cuff problems. Stage 2 SAS patients were included in the study and only one phase of GMI treatment was used in addition to the traditional physiotherapy program. Despite these positive results in favor of GMI, the fact that there is no study using the entire GMI treatment in SAS shows us that a randomized controlled and blinded study with high evidence value should be conducted on this subject. In addition, determining the effect of GMI on changes in central nervous system such as fear of pain, two-point discrimination, and left\u002Fright lateralization speed and accuracy task will help fill the literature gaps on this subject. In the light of this information, the question of planned master's thesis study is the effect of GMI treatment applied in addition to traditional physiotherapy in SAS on pain level, joint range of motion, functionality, pain-related fear, two-point discrimination and left\u002Fright lateralization speed and accuracy compared to only traditional physiotherapy. whether it is superior or not.",[149,27],[149,291],"graded motor imagery","2024-07-10",{"date":294,"type":43},"2024-07-11",{"date":296,"type":43},"2023-10-13",{"date":298,"type":23},"2025-12-13",{"name":300,"class":50},"Nuray Alaca"]