[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"shoulder-impingement\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:shoulder-impingement":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,42,70],{"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":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100561225","comparison-of-manual-therapy-versus-radial-shock-waves-in-the-shoulder-pain-treatment-100561225",false,"NCT06587399","Comparison of Manual Therapy Versus Radial Shock Waves in the Shoulder Pain Treatment","Comparison of Manual Therapy Versus Low-medium Energy Radial Shock Waves in the Treatment of Subacromial Syndrome in a Randomized Clinical Trial","Inclusion Criteria:\n\n* Unilateral shoulder pain with no history of trauma.\n* Pain of at least 4\u002F10 on the Visual Analogue Scale for a minimum period of 3 months.\n* Be positive in at least 3 of the following 5 tests: painful arc test, Neer impingement test, Hawkins-Kennedy test, Jobe test, external rotation test against resistance for the infraspinatus tendon.\n\nExclusion Criteria:\n\n* Presence of red flags.\n* Diagnosis of shoulder instability.\n* Diagnosis of frozen shoulder.\n* Diagnosis of complete rupture of the common rotator cuff tendon.\n* Diagnosis of cervical radiculopathy.\n* Diagnosis of whiplash.\n* Diagnosis of degenerative disease of the glenohumeral joint.","ALL","18 Years","80 Years",{"count":20,"type":21},88,"ESTIMATED","INTERVENTIONAL",[24],"NA","Subacromial syndrome represents the third leading cause of pain in the general population. There is no clear pathophysiological explanation, nor a specific treatment. Manual therapy stands out as one of the reference treatments for this disease, however, it is complex to develop a specific protocol. On the other hand, shock waves have still not received adequate attention in the treatment of this pathology. The aim of this study will focus on using manual treatment using ischemic pressure, joint mobilizations and myofascial techniques in comparison to shock wave therapy to determine which is more effective.\n\nThis study will be a randomized, single-blind clinical trial with third-party evaluation. In it 88 subjects suffering from subacromial syndrome will participate. 44 patients will receive treatment through manual therapy over 6 weeks and other 44 patients through low-med energy radial shock waves for 6 weeks.\n\nAll subjects will complete their treatment with a 12-week home-based therapeutic exercise program.\n\nThe main endpoint of the study will be pain measured using the visual analogue scale (VAS) in motion. Pain will also be assessed using the VAS scale at rest and overnight. The Spadi Spanish version questionnaire will be used, shoulder strength will be measured using a handheld dynamometer and the ranges of motion will be measured.\n\nData will be measured before and one year after treatment.",[27,28],"Shoulder Impingement","Shoulder Pain","RECRUITING","2025-06-01",{"date":32,"type":33},"2025-06-03","ACTUAL",{"date":35,"type":33},"2024-09-30",{"date":37,"type":21},"2026-09-15",{"name":39,"class":40},"University of Alcala","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":46,"acronym":47,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":16,"minAge":49,"maxAge":50,"enrollmentInfo":51,"targetDuration":4,"studyType":53,"phases":4,"briefSummary":54,"conditions":55,"keywords":56,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":66,"leadSponsor":68,"locationsCount":4},"100592836","correlation-between-shoulder-impingement-and-cervical-proprioception-100592836","NCT06998615","Correlation Between Shoulder Impingement and Cervical Proprioception","CP","Inclusion Criteria:\n\n* Diagnosis: Patients diagnosed with shoulder impingement\n* Age: Patients aged between 25 and 45 years.\n* Pain and mobility issues: Patients must report mild to moderate pain and\u002For restricted range of motion (ROM) in shoulder joint .\n* Ability to provide informed consent: Participants must be able to understand the study protocol and provide written informed consent to participate.\n* Medical stability: Patients must be medically stable and able to engage in physical assessment\n\nExclusion Criteria:\n\n* any patient aged below 25 or above 45 years old\n* Subjects have malignancy: Patients with severe neurological, musculoskeletal, disorders that could interfere with the study interventions\n* Subjects have history of shoulder trauma, fractures and surgeries:\n* Subjects have neck dysfunction\n* Cognitive impairment: Patients with significant cognitive impairment or mental health conditions that would hinder their ability to understand or comply with the study protocol.","25 Years","45 Years",{"count":52,"type":21},68,"OBSERVATIONAL","this study will be conducted to evaluate the correlation between shoulder impingement and cervical proprioception",[27],[57,58,59,60],"shoulder impingement","neck proprioception","correlation","cervical proprioception","NOT_YET_RECRUITING","2025-05-30",{"date":64,"type":33},"2025-06-04",{"date":62,"type":21},{"date":67,"type":21},"2025-07-30",{"name":69,"class":40},"Cairo University",{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":22,"phases":79,"briefSummary":80,"conditions":81,"keywords":4,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":4},"100564172","analysis-of-sleep--recovery-following-rotator-cuff-repair-surgery-100564172","NCT06625723","Analysis of Sleep & Recovery Following Rotator Cuff Repair Surgery","Investigating the Impact of a Sleep Aid on Sleep and Recovery Following Rotator Cuff Repair Surgery","Inclusion Criteria:\n\n* Rotator Cuff Tear\n\nExclusion Criteria:\n\n* Prior ipsilateral shoulder surgery\n* Ipsilateral upper extremity neurological deficit",{"count":78,"type":21},60,[24],"Postoperative recovery following a rotator cuff repair surgery can be challenging. In particular, sleeping is difficult given the restrictions of the operative shoulder. This study aims to evaluate a postoperative sleep device that will allow for safe and comfortable positioning of the arm, with the anticipated effect to improve postoperative recovery and sleep.",[82,83,28,84,27],"Rotator Cuff Tears","Rotator Cuff Injuries","Shoulder Injuries","2024-11-14",{"date":87,"type":33},"2024-11-18",{"date":89,"type":21},"2024-12-01",{"date":91,"type":21},"2027-04-01",{"name":93,"class":40},"New York Presbyterian Hospital"]