[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"subacromial-pain-syndrome\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:subacromial-pain-syndrome":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,12,0,[8,45,67,94,123,143,166,191,214,242,267,294],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100547551","effects-of-corrective-external-support-and-regional-vibration-applications-in-subacromial-pain-syndrome-100547551",false,"NCT06409442","Effects of Corrective External Support and Regional Vibration Applications in Subacromial Pain Syndrome","Effects of Corrective External Support and Regional Vibration Applications Added to the Rehabilitation Program in Subacromial Pain Syndrome: Randomized Controlled Study","Inclusion Criteria:\n\n* Volunteering to participate in the study,\n* Being over 18 years of age,\n* Having diagnosed with subacromial impingement syndrome,\n* SIS-related complaints have persisted for at least 3 months,\n* Not having received any treatment for shoulder problems in the last 6 months,\n* No history of shoulder injury other than subacromial impingement and\u002For shoulder symptoms requiring treatment for the last 1 year,\n* To be able to read and write Turkish in order to complete all evaluations and applications in the study and to carry out evaluations that require reading and writing.\n\nExclusion Criteria:\n\n* Having a history of fractures and surgery in the upper extremity and cervicothoracic region,\n* Having another neurological, orthopedic or rheumatic shoulder problem such as frozen shoulder or instability,\n* Having a systemic musculoskeletal disease,\n* Known chest deformity, scoliosis diagnosis and physical disability,\n* Presence of a skin problem or a condition that may be a contraindication to the application in the area where KT or LVT will be applied.","ALL","18 Years",{"count":19,"type":20},63,"ESTIMATED","INTERVENTIONAL",[23],"NA","Sixty three individuals with chronic subacromial pain syndrome will be included in our study. In the evaluations to be made to the participants; Pain intensity will be measured with the Visual Analogue Scale (VAS), joint movement and shoulder proprioception will be measured with the inclinometer, and shoulder muscle strength will be measured with the digital hand dynamometer. In addition, functionality and disability levels will be determined by SPADI and Short form-Questionnaire for Arm, Shoulder and Hand Problems (Q-DASH). Supraspinatus tendon thickness and acromiohumeral space measurements will be made by ultrasonographic imaging. Patient satisfaction will be evaluated with the Visual Analog Patient Satisfaction Scale survey and quality of life will be evaluated with the SF-12 survey (The 12-item Short Form Survey).\n\nParticipants will be randomly divided into 3 groups of 21 participants each. In addition to the standard physiotherapy program, taping around the shoulder will be applied to the kinesio taping group, and localized vibration therapy around the shoulder will be applied to the localized vibration therapy group, in addition to the standard physiotherapy program. The Control Group (CG) will receive the same physiotherapy program as the other groups and will attend the same number of sessions as the other groups, accompanied by a physiotherapist. Evaluations will be made and analyzed before treatment, after 3 weeks of treatment, after 6 weeks of treatment, at 12 weeks and at the end of 24 weeks.",[26],"Subacromial Pain Syndrome",[28,29,30,31],"shoulder impingement syndrome","pain","physical therapy and rehabilitation","ultrasonography","RECRUITING","2026-06-23",{"date":35,"type":36},"2026-06-26","ACTUAL",{"date":38,"type":36},"2024-06-24",{"date":40,"type":20},"2027-05-30",{"name":42,"class":43},"Dokuz Eylul University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":51,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":55,"phases":4,"briefSummary":56,"conditions":57,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":44},"100642755","the-effect-of-unstable-loads-on-scapular-kinematics-and-muscle-activation-during-overhead-press-in-overhead-athletes-with-subacromial-pain-syndrome-100642755","NCT07646899","The Effect of Unstable Loads on Scapular Kinematics and Muscle Activation During Overhead Press in Overhead Athletes With Subacromial Pain Syndrome","The inclusion criteria for both the experimental and control groups were as follows: (1) amateur or recreational overhead athletes aged 18-40 years (e.g., volleyball, tennis, baseball); (2) sport participation history of more than 3 years; (3) weekly overhead sport participation of more than 4 hours; (4) ability to meet the minimum loading requirements of the equipment for both stable and unstable conditions, defined as a 15-repetition maximum (15RM) for stable shoulder press of ≥10 kg and unstable shoulder press of ≥8 kg.\n\nThe individual inclusion criteria for the experimental group were: (1) diagnosis of subacromial pain syndrome, defined as at least 3 positive findings out of 5 clinical tests (Painful Arc test, Neer impingement test, Empty Can test, Hawkins-Kennedy impingement test, and Resisted External Rotation test); (2) Visual Analogue Scale (VAS) score of ≤3 during shoulder press performance; (3) symptoms present on the dominant side.\n\nThe individual inclusion criteria for the control group were: absence of shoulder pain within the past 6 months, including no pain at the glenohumeral joint, acromioclavicular joint, sternoclavicular joint, scapulothoracic joint, or cervical spine.\n\nThe exclusion criteria were as follows: (1) history of surgical intervention for fracture or dislocation of the shoulder or elbow joint within the past 6 months; (2) direct trauma to the cervical spine or upper extremity within the past 1 month; (3) shoulder pain or neurological symptoms of cervical origin; (4) any condition preventing the completion of the experimental protocol; (5) bilateral shoulder pain.",true,"40 Years",{"count":54,"type":20},27,"OBSERVATIONAL","The research aims to compare the differences between stable and unstable load conditions during shoulder pressing in overhead athletes with SAPS and to compare the differences between SAPS and healthy athletes with stable and unstable load conditions.",[26],"2026-06-09",{"date":60,"type":36},"2026-06-15",{"date":62,"type":36},"2024-09-26",{"date":64,"type":20},"2026-06-30",{"name":66,"class":43},"National Yang Ming Chiao Tung University",{"id":68,"slug":69,"hasResults":11,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":4,"eligibilityCriteria":73,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":74,"targetDuration":4,"studyType":21,"phases":76,"briefSummary":77,"conditions":78,"keywords":79,"overallStatus":84,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":44},"100637677","effects-of-dry-needling-in-athletes-with-subacromial-pain-syndrome-100637677","NCT07621016","Effects of Dry Needling in Athletes With Subacromial Pain Syndrome","Effects of Dry Needling on Proprioception, Dynamic Stability, Strength, Pain Perception, and Disability in Athletes With Subacromial Pain Syndrome","Inclusion Criteria:\n\n* Men and women aged between 18 and 40 years.\n* Clinical diagnosis of subacromial pain syndrome (SAPS) according to the Dutch Orthopaedic Association criteria: presence of a painful arc and at least two positive tests among the following: Hawkins-Kennedy test, Neer sign, Jobe test, Drop Arm test, or Gerber test.\n* Participation in sports involving predominant upper-limb activity between 2 and 4 hours per week.\n\nExclusion Criteria:\n\n* Previous surgery involving the upper extremities.\n* Diagnosis of specific shoulder pathologies other than SAPS at the time of the study.\n* Receipt of medical or physiotherapy treatment within the month prior to the intervention.\n* Needle phobia or refusal to receive dry needling treatment.\n* Presence of vestibular disorders, balance impairments, or vascular alterations that could interfere with study measurements.\n* Confirmed or suspected pregnancy.",{"count":75,"type":20},40,[23],"The goal of this clinical trial is to evaluate whether dry needling combined with therapeutic exercise improves shoulder proprioception in amateur athletes with subacromial pain syndrome. The study will also assess its effects on dynamic stability, strength, pain, and functional disability.\n\nThe main questions this study aims to answer are:\n\nDoes dry needling improve shoulder proprioception compared with therapeutic exercise alone? Does dry needling improve dynamic shoulder stability and muscle strength? Does dry needling reduce pain and upper limb disability?\n\nResearchers will compare a group receiving dry needling plus therapeutic exercise with a group performing therapeutic exercise alone to determine whether the combined intervention produces better outcomes.\n\nParticipants will:\n\nBe randomly assigned to one of the two treatment groups. Perform a home-based therapeutic exercise program for 3 weeks. Complete assessments of proprioception, dynamic stability, strength, pain, and functional disability before and after the intervention.",[26],[80,81,82,83],"subacromial pain syndrome","dry needling","shoulder proprioception","shoulder pain","NOT_YET_RECRUITING","2026-06-03",{"date":87,"type":36},"2026-06-05",{"date":89,"type":20},"2026-06",{"date":91,"type":20},"2027-03",{"name":93,"class":43},"Universidad Europea de Valencia",{"id":95,"slug":96,"hasResults":11,"nctId":97,"briefTitle":98,"officialTitle":98,"acronym":4,"eligibilityCriteria":99,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":100,"enrollmentInfo":101,"targetDuration":4,"studyType":21,"phases":103,"briefSummary":104,"conditions":105,"keywords":110,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":115,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":44},"100634930","the-effect-of-an-exercise-program-based-on-attentional-focus-shifting-on-clinical-outcomes-in-rotator-cuff-related-shoulder-pain-100634930","NCT07546084","The Effect of an Exercise Program Based on Attentional Focus Shifting on Clinical Outcomes in Rotator Cuff Related Shoulder Pain","Inclusion Criteria:\n\n* Having symptoms persisting for at least 3 months\n* Experiencing pain intensity of at least 3 on the Numeric Pain Rating Scale (NPRS) during activity\n* Presence of a painful arc during shoulder flexion or abduction\n* Positive Neer test or Hawkins-Kennedy test\n* Pain provoked by resisted external rotation\u002Fabduction of the humerus, or a positive Jobe (Empty Can) test\n* Having a clinical diagnosis of subacromial pain syndrome, rotator cuff tendinopathy, subacromial bursitis, or symptomatic partial\u002Ffull-thickness rotator cuff tear\n* Being able to understand and complete questionnaires in Turkish\n\nExclusion Criteria:\n\n* Presence of adhesive capsulitis (≥30% limitation in passive range of motion)\n* Advanced osteoarthritis of the shoulder\n* History of fracture or dislocation affecting the shoulder region\n* Advanced acromioclavicular joint pathology\n* Massive rotator cuff tear (positive lag signs)\n* Previous shoulder surgery\n* Presence of neurological disorders\n* Diagnosis of rheumatoid arthritis\n* History of cancer\n* Symptomatic cervical spine pathology\n* Corticosteroid injection to the shoulder within the past 6 weeks\n* Cognitive impairments that may interfere with the ability to perform clinical tasks or execute attention shift-based exercises","65 Years",{"count":102,"type":20},46,[23],"The aim of this clinical trial is to investigate the effects of an attention shift-based rehabilitation program on clinical outcomes in individuals with rotator cuff-related shoulder pain (RCRSP). The study will evaluate the effects of an attention shift approach, in which motor tasks targeting regions outside the shoulder are performed concurrently with standard shoulder exercises, on pain, functional status, and pain catastrophizing. These results will be compared with those of a standard shoulder rehabilitation program.\n\nThe main questions this study aims to answer are:\n\nIs there a difference in pain levels between individuals with RCRSP who participate in an attention shift-based rehabilitation program and those who participate in a standard exercise program? Is there a difference between these two rehabilitation approaches in terms of shoulder function and pain catastrophizing?\n\nParticipants will:\n\nBe randomly assigned to either an attention shift-based rehabilitation group or a standard shoulder rehabilitation group Participate in supervised exercise sessions twice per week for 6 weeks Attend sessions lasting approximately 60-75 minutes Undergo clinical assessments at baseline and at week 6",[106,26,107,108,109],"Rotator Cuff Related Shoulder Pain","Shoulder Bursitis","Shoulder Tendinopathy","Rotator Cuff Tears of the Shoulder",[111,112,113],"Rotator cuff","Shoulder pain","attention shift","2026-04-20",{"date":116,"type":36},"2026-04-22",{"date":118,"type":20},"2026-05-15",{"date":120,"type":20},"2027-06-15",{"name":122,"class":43},"Istanbul University",{"id":124,"slug":125,"hasResults":11,"nctId":126,"briefTitle":127,"officialTitle":127,"acronym":4,"eligibilityCriteria":128,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":100,"enrollmentInfo":129,"targetDuration":4,"studyType":21,"phases":130,"briefSummary":131,"conditions":132,"keywords":134,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":136,"lastUpdatePostDateStruct":137,"startDateStruct":138,"completionDateStruct":140,"leadSponsor":142,"locationsCount":44},"100624925","the-effect-of-a-dual-task-technique-based-exercise-program-on-clinical-outcomes-in-rotator-cuff-related-shoulder-pain-100624925","NCT07415967","The Effect of a Dual-Task Technique-Based Exercise Program on Clinical Outcomes in Rotator Cuff Related Shoulder Pain","Inclusion Criteria:\n\n* Aged between 18 and 65 years\n* Diagnosis of impingement syndrome, subacromial bursitis, rotator cuff tendinopathy, or partial rotator cuff tear\n* Shoulder pain level ≥3 according to the Numeric Pain Rating Scale (NPRS)\n* Shoulder pain persisting for at least 3 months\n\nExclusion Criteria:\n\n* Diagnosis of shoulder instability, adhesive capsulitis, or full-thickness or massive rotator cuff tear\n* Presence of musculoskeletal, neurological, and\u002For psychological conditions that would prevent participation in an exercise program\n* History of shoulder surgery\n* Having received physiotherapy or corticosteroid injection treatment for shoulder pain within the past 6 months\n* Presence of cognitive impairment that would prevent participation in dual-task exercise activities",{"count":102,"type":20},[23],"The aim of this clinical trial is to investigate the effects of a dual-task-based exercise program on clinical outcomes in individuals with rotator cuff-related shoulder pain. The study will evaluate the effects of a dual-task exercise approach, in which physical exercises are performed concurrently with cognitive tasks, on pain, functional status, pain catastrophizing and kinesiophobia. These results will be compared with those of a standard shoulder rehabilitation program. The main questions this study aims to answer are:\n\n* Is there a difference in pain levels between individuals with rotator cuff-related shoulder pain who participate in a dual-task-based exercise program and those who participate in a standard exercise program?\n* Is there a difference between these two exercise approaches in terms of shoulder function and psychosocial factors?\n\nParticipants will:\n\n* Participate in either a dual-task-based shoulder exercise program or a standard shoulder exercise program twice per week for 6 weeks.\n* Undergo clinical assessments at baseline, at week 6, and at week 12.",[106,133,26],"Shoulder Pain Syndrome",[111,112,135],"Dual-task exercise","2026-04-15",{"date":114,"type":36},{"date":139,"type":36},"2026-02-16",{"date":141,"type":20},"2027-06-16",{"name":122,"class":43},{"id":144,"slug":145,"hasResults":11,"nctId":146,"briefTitle":147,"officialTitle":148,"acronym":4,"eligibilityCriteria":149,"healthyVolunteers":11,"sex":16,"minAge":150,"maxAge":4,"enrollmentInfo":151,"targetDuration":4,"studyType":55,"phases":4,"briefSummary":153,"conditions":154,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":157,"lastUpdatePostDateStruct":158,"startDateStruct":160,"completionDateStruct":162,"leadSponsor":163,"locationsCount":44},"100597333","neuropathic-characteristics-of-subacromial-pain-syndrome-100597333","NCT07057128","Neuropathic Characteristics of Subacromial Pain Syndrome","Descriptors of Neuropathic Pain and Its Association With Central Sensitization in Subacromial Pain Syndrome","Inclusion Criteria:\n\n1. Clinical diagnosis of subacromial pain syndrome (SAPS)\n2. Age ≥ 19 years\n3. Shoulder pain lasting for at least 3 months\n4. Shoulder pain intensity rated as 3 or higher on the Visual Analog Scale (VAS) in the past week\n5. Positive findings on the following clinical tests:\n\nHawkins-Kennedy test Painful arc test Infraspinatus muscle strength test\n\nExclusion Criteria:\n\n1. History of inflammatory disease involving the shoulder joint\n2. History of neurological disorders\n3. History of prior shoulder surgery\n4. Positive drop arm test\n5. Loss of passive range of motion in the shoulder joint\n6. Presence of muscle strength loss\n7. Structurally confirmed shoulder pathology based on imaging studies\n8. Full-thickness tear of the rotator cuff muscles\n9. Presence of neurodeficit in the upper extremity\n10. Diagnosis of cancer or active infection\n11. Use of medications for neuropathic pain within the past 3 months for any reason","19 Years",{"count":152,"type":20},82,"This single-center observational study aims to investigate neuropathic pain descriptors and their relationship with central sensitization in patients diagnosed with subacromial pain syndrome (SAPS) who have had shoulder pain for at least 3 months. A total of 82 participants aged 19 years or older will be recruited from the Physical Medicine and Rehabilitation outpatient clinic of Izmir City Hospital. After obtaining informed consent, participants will complete validated questionnaires assessing pain severity (VAS), neuropathic pain characteristics (painDETECT), central sensitization (Central Sensitization Inventory), and shoulder function (SPADI). Range of motion will be measured using a goniometer. No imaging or invasive procedures will be performed. Using the central sensitization scale and pain detect, the presence or absence of the 7 pain descriptors will be investigated in patients with subacromial pain syndrome with or without central sensitization and neuropathic pain pattern and it will be investigated whether the contribution of hyperalgesia, one of these pain descriptors, to neuropathic pain and central sensitization in patients with subacromial pain syndrome is greater than the contribution of other pain descriptors.The results of this study are expected to provide insight into pain mechanisms and guide clinical management in patients with SAPS.",[155,156,26],"Neuropathic Pain","Central Sensitization","2026-04-12",{"date":159,"type":36},"2026-04-14",{"date":161,"type":36},"2025-09-15",{"date":89,"type":20},{"name":164,"class":165},"Izmir City Hospital","OTHER_GOV",{"id":167,"slug":168,"hasResults":11,"nctId":169,"briefTitle":170,"officialTitle":171,"acronym":4,"eligibilityCriteria":172,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":173,"enrollmentInfo":174,"targetDuration":4,"studyType":21,"phases":176,"briefSummary":177,"conditions":178,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":182,"lastUpdatePostDateStruct":183,"startDateStruct":185,"completionDateStruct":187,"leadSponsor":189,"locationsCount":44},"100433388","therapeutic-exercise-for-rotator-cuff-tendinopathy--subacromial-pain-syndrome---outcomes-and-mechanisms-100433388","NCT04923477","Therapeutic Exercise for Rotator Cuff Tendinopathy \u002F Subacromial Pain Syndrome - Outcomes and Mechanisms","Mechanisms of Exercise for Rotator Cuff Tendinopathy \u002F Subacromial Pain Syndrome","Inclusion Criteria:\n\n1. the clinical diagnosis for RC tendinopathy will be made with positive 3 of 5 tests: Hawkins-Kennedy, Neer, painful arc, empty can, external rotation resistance test\n2. pain ≥ 3\u002F10 on a numeric pain rating scale\n3. age: 18 - 45 years\n4. Participant must read, sign and date the appropriate Informed consent document.\n5. Participant BMI ≤ 30\n\nExclusion Criteria:\n\n1. Insufficient ability to comprehend and complete the questionnaires,\n2. Inability to attend sessions,\n3. Prior surgery of shoulder, neck or thoracic spine,\n4. Primary complaint of neck or thoracic pain,\n5. Diagnosis of cervical spinal stenosis,\n6. Any serious spinal and shoulder pathology: infections, arthrosis, rheumatic disorders, acute fractures, shoulder dislocation, osteoporosis, or tumors,\n7. 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 and\u002For Babinski reflexes,\n8. two or more neurologic signs of nerve root compression to include myotomal weakness, positive muscle stretch reflex, and dermatomal sensory loss,\n9. any shoulder or arm pain with cervical spine tests of Spurling's Test, cervical rotation to the ipsilateral side, or axial compression test, or\n10. primary adhesive capsulitis defined by passive range of motion loss \\>50% as compared bilaterally of shoulder external rotation, internal rotation, or elevation.\n11. Has a device or other condition that is not safe for MRI, including pacemakers.","55 Years",{"count":175,"type":20},60,[23],"Rotator cuff tendinopathy, one of the pathologies identified as part of the cluster of shoulder symptoms known as subacromial pain syndrome, is a common musculoskeletal shoulder condition. Resolution of pain and disability is poor despite treatment, with only about 50% reporting full recovery at 12 - 18 months. Prior studies suggest therapeutic exercise when used alone and with other interventions can have positive outcomes; however, not all patients with rotator cuff tendinopathy respond. Few studies have assessed the effects of exercise for individuals with chronic pain, especially brain driven mechanisms, thought to play a key role. In this study, we will use brain imaging to understand the mechanisms, identify predictors of a positive response to exercise, and the relationship to biomechanical and pain-related factors in patients with RC tendinopathy. The findings from this study will optimize the delivery and treatment response to exercise for individuals with shoulder pain.",[179,180,181,26],"Rotator Cuff Tendinosis","Rotator Cuff Tendinitis","Rotator Cuff Injuries","2026-01-30",{"date":184,"type":36},"2026-02-03",{"date":186,"type":36},"2021-06-08",{"date":188,"type":20},"2026-12-31",{"name":190,"class":43},"University of Southern California",{"id":192,"slug":193,"hasResults":11,"nctId":194,"briefTitle":195,"officialTitle":195,"acronym":4,"eligibilityCriteria":196,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":100,"enrollmentInfo":197,"targetDuration":4,"studyType":21,"phases":199,"briefSummary":200,"conditions":201,"keywords":203,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":205,"lastUpdatePostDateStruct":206,"startDateStruct":208,"completionDateStruct":210,"leadSponsor":212,"locationsCount":44},"100617878","which-patient-group-shows-greater-improvement-with-patient-education-alone-in-rotator-cuff-related-shoulder-pain---a-cohort-study-100617878","NCT07324343","Which Patient Group Shows Greater Improvement With Patient Education Alone in Rotator Cuff-Related Shoulder Pain? - A Cohort Study","Inclusion Criteria:\n\n* Individuals aged 18-65 years\n* Shoulder pain persisting for at least 4 weeks\n* Diagnosed by an orthopedic physician with impingement, subacromial bursitis, rotator cuff (RC) tendinopathy, or partial tear\n* Activity-related pain ≥3 on the NPRS\n* Cognitively able to understand the education and provide written informed consent\n\nExclusion Criteria:\n\n* History of shoulder surgery\n* Diagnosis of frozen shoulder, full-thickness or massive rotator cuff (RC) tear, or instability\n* Presence of neurological or psychiatric conditions that prevent exercise\n* History of physical therapy-rehabilitation or injection treatment within the past 6 months\n* Pain persisting for more than 12 months",{"count":198,"type":20},116,[23],"The primary aim of this study is to determine the clinical effectiveness of patient education alone in individuals with rotator cuff-related shoulder pain and to identify which patient subgroups benefit more from this approach. In addition, the translation and cultural adaptation of the \"Patient Knowledge Questionnaire (PKQ-RCRSP)\" into Turkish will be carried out to measure the level of patient knowledge regarding patient education.",[133,26,106,202],"Patient Education",[204,106],"patient education","2025-12-24",{"date":207,"type":36},"2026-01-07",{"date":209,"type":36},"2025-09-01",{"date":211,"type":20},"2026-12-01",{"name":213,"class":43},"Istanbul University - Cerrahpasa",{"id":215,"slug":216,"hasResults":11,"nctId":217,"briefTitle":218,"officialTitle":219,"acronym":4,"eligibilityCriteria":220,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":100,"enrollmentInfo":221,"targetDuration":4,"studyType":21,"phases":223,"briefSummary":224,"conditions":225,"keywords":226,"overallStatus":84,"whyStopped":4,"lastUpdateSubmitDate":233,"lastUpdatePostDateStruct":234,"startDateStruct":236,"completionDateStruct":238,"leadSponsor":240,"locationsCount":4},"100597834","predictive-model-for-pens-response-in-subacromial-pain-syndrome-100597834","NCT07063641","Predictive Model for PENS Response in Subacromial Pain Syndrome","Development of a Predictive Model to Identify Clinical Factors Associated With Response to Percutaneous Electrical Nerve Stimulation in Patients With Subacromial Pain Syndrome","Inclusion Criteria:\n\nAdults aged between 18 and 65 years.\n\nClinical diagnosis of subacromial pain syndrome (SAPS), based on the following clinical criteria:\n\n* Pain localized to the anterolateral shoulder region.\n* Symptoms present for more than 6 weeks.\n* Painful arc during shoulder abduction.\n* Positive Neer or Hawkins-Kennedy impingement signs.\n* Positive Jobe (empty can) test or external rotation resistance test.\n\nVisual Analogue Scale (VAS) for shoulder pain ≥ 3\u002F10 in the previous week.\n\nAble to understand study procedures and sign informed consent.\n\nExclusion Criteria:\n\n* Bilateral shoulder pain.\n* History of fracture, dislocation, or surgical intervention on the affected shoulder.\n* Presence of other shoulder pathologies such as adhesive capsulitis (frozen shoulder), glenohumeral instability, or full-thickness rotator cuff tear.\n* Medical contraindications for PENS application (e.g., active anticoagulation, pregnancy, or decompensated psychiatric condition).\n* Diagnosed cervical radiculopathy or myelopathy.\n* Neurological or cognitive disorders interfering with study participation.\n* Presence of chronic widespread pain syndromes, such as fibromyalgia.\n* Belonephobia (severe needle phobia) that prevents intervention.",{"count":222,"type":20},269,[23],"Subacromial pain syndrome (SPS) is one of the most common causes of shoulder pain, leading to significant disability and socioeconomic burden. Although percutaneous electrical nerve stimulation (PENS) targeting the suprascapular nerve (SN) has shown positive therapeutic outcomes, individual response to the intervention varies considerably. This study aims to develop a multivariable predictive model to estimate clinical response to SN-targeted PENS in patients with SPS. The model will be built using clinical, psychological, and neural mechanosensitivity variables. The goal is to enhance patient selection and guide personalized treatment strategies.",[26,106],[227,228,229,230,231,232],"Percutaneous Electrical Nerve Stimulation","Suprascapular Nerve","Neural Mechanosensitivity","Musculoskeletal Pain","Ultrasound-Guided Interventions","Subacromial pain syndrome","2025-07-03",{"date":235,"type":36},"2025-07-14",{"date":237,"type":20},"2025-09-20",{"date":239,"type":20},"2026-11-10",{"name":241,"class":43},"Néstor Requejo Salinas",{"id":243,"slug":244,"hasResults":11,"nctId":245,"briefTitle":246,"officialTitle":247,"acronym":4,"eligibilityCriteria":248,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":249,"enrollmentInfo":250,"targetDuration":4,"studyType":21,"phases":252,"briefSummary":253,"conditions":254,"keywords":255,"overallStatus":84,"whyStopped":4,"lastUpdateSubmitDate":258,"lastUpdatePostDateStruct":259,"startDateStruct":261,"completionDateStruct":263,"leadSponsor":265,"locationsCount":44},"100596314","effect-of-thoracic-mobility-exercises-combined-with-scapular-stabilization-exercises-in-individuals-with-subacromial-pain-syndrome-100596314","NCT07043842","Effect of Thoracic Mobility Exercises Combined With Scapular Stabilization Exercises in Individuals With Subacromial Pain Syndrome","Effects of Thoracic Mobility Exercises Combined With Scapular Stabilization Exercises on Pain, Range of Motion, Scapular Alignment, Postural Alignment and Quality of Life in Individuals With Subacromial Pain Syndrome","Inclusion Criteria:\n\n* Volunteering to participate in the study\n* Being between the ages of 18-60\n* Being diagnosed with subacromial pain syndrome\n* Having Stage I or Stage II subacromial pain syndrome according to Neer\n* Having unilateral shoulder pain that limits activity for more than 6 weeks\n* Having pain intensity over 3 according to VAS\n\nExclusion Criteria:\n\n* Having cervical radiculopathy\n* Having spinal deformities\n* Having post-traumatic symptom onset\n* Having a history of shoulder dislocation or fracture\n* Having passive joint movement limitation (frozen shoulder)\n* Having received steroid injections within the last 6 weeks\n* Having degenerative joint disease of the shoulder joint complex, having a history of surgical intervention to the shoulder joint complex, having any diagnosed rheumatic, systemic or neurological disease\n* Having cardiovascular pathologies that limit rehabilitation","60 Years",{"count":251,"type":20},20,[23],"The subject of this study is to examine the effects of thoracic mobility exercises combined with scapular stabilization exercises on pain, range of motion, scapular alignment, postural alignment and quality of life in individuals with subacromial pain syndrome.\n\nThe scapula assumes a role that is attached to the axial skeleton by atmospheric pressure and axioscapular muscles, and prepares the ground for the formation of wide range of motion in the shoulder complex. The scapulothoracic movement formed by the movement of the scapula on the thorax is provided not only by the function of the scapular muscles but also by the optimization of the thoracic muscles and posture.\n\nTherefore, changes in the biomechanics of the thoracic spine and scapula affect the function of the shoulder. Therefore, we predict that the possible contributions of scapular stabilization and thoracic mobility exercises to scapular alignment and alignment in thoracic posture will further improve shoulder-related complaints.",[26],[80,256,257],"scapular stabilization exercises","thoracic mobility exercises","2025-06-21",{"date":260,"type":36},"2025-06-29",{"date":262,"type":20},"2025-07-28",{"date":264,"type":20},"2026-09-28",{"name":266,"class":43},"Ankara Yildirim Beyazıt University",{"id":268,"slug":269,"hasResults":11,"nctId":270,"briefTitle":271,"officialTitle":272,"acronym":4,"eligibilityCriteria":273,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":274,"enrollmentInfo":275,"targetDuration":4,"studyType":21,"phases":277,"briefSummary":278,"conditions":279,"keywords":282,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":286,"lastUpdatePostDateStruct":287,"startDateStruct":289,"completionDateStruct":291,"leadSponsor":293,"locationsCount":44},"100550627","the-effect-of-the-treatment-environment-on-pain-function-self-efficacy-and-satisfaction-in-rcrsp-100550627","NCT06449534","The Effect of the Treatment Environment on Pain, Function, Self Efficacy and Satisfaction in RCRSP","The Effect of the Treatment Environment on Pain, Function, Self Efficacy and Satisfaction in Rotator Cuff Related Shoulder Pain","Inclusion Criteria:\n\n* 18-75 years old\n* diagnosed with impingement syndrome, subacromial bursitis, rotator cuff tendinopathy or partial rotator cuff tear\n* pain level between 3-7 according to visual analog scale\n* pain persisted for at least 3 months\n\nExclusion Criteria:\n\n* having a full-thickness or massive rotator cuff tear\n* history of shoulder surgery\n* having a musculoskeletal disease that prevents exercise\n* having a neurological disease or psychological disorder","75 Years",{"count":276,"type":20},34,[23],"Brief Summary\n\nThe aim of this randomized controlled study is to reveal the short-term effects of physical and social factors in different therapeutic environments on patients with rotator cuff related shoulder pain following the same exercise program. The main questions it aims answer are:\n\n* Is there any difference in terms of pain levels among groups with rotator cuff related shoulder pain who treated in different therapeutic settings.\n* Is there any difference in terms of functionality and self-efficacy among groups with rotator cuff related shoulder pain who treated in different therapeutic settings.",[280,26,281],"Shoulder Pain","Rotator Cuff Syndrome of Shoulder and Allied Disorders",[283,284,285],"Therapeutic Environment","Contextual Factors","Exercise Therapy","2024-10-01",{"date":288,"type":36},"2024-10-03",{"date":290,"type":36},"2024-05-06",{"date":292,"type":20},"2025-05-15",{"name":213,"class":43},{"id":295,"slug":296,"hasResults":11,"nctId":297,"briefTitle":298,"officialTitle":299,"acronym":300,"eligibilityCriteria":301,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":302,"targetDuration":4,"studyType":21,"phases":304,"briefSummary":305,"conditions":306,"keywords":308,"overallStatus":84,"whyStopped":4,"lastUpdateSubmitDate":314,"lastUpdatePostDateStruct":315,"startDateStruct":317,"completionDateStruct":319,"leadSponsor":321,"locationsCount":44},"100537312","digital-physiotherapy-treatment-for-patients-with-subacromial-pain-compared-to-usual-physiotherapy-in-primary-care-100537312","NCT06276192","Digital Physiotherapy Treatment for Patients With Subacromial Pain Compared to Usual Physiotherapy in Primary Care","Digital Physiotherapy Treatment for Patients With Subacromial Pain Compared to Traditional Physiotherapy Treatment in Primary Care - a Non-Inferiority Randomised Controlled Trial","diSAID","Inclusion Criteria:\n\n* \\>18 years old\n* Pain duration \\>2 weeks\n* Lateral shoulder pain (C5 dermatome)\n\nAt least three positive tests as follows:\n\n* Painful arc\n* External rotation resistance test\n* Jobe's test\n* Neer's impingement sign\n* Hawkin's-Kennedy's impingement test\n\nExclusion Criteria:\n\n* Symptoms are related to a traumatic event in the last 6 months with suspected rotator cuff tear, dislocation or fracture.\n* Clinical features of cervical radiculopathy\n* Clinical features of Adhesive capsulitis\n* The patient does not understand or can not read Swedish\n* The patient has no access to BankID",{"count":303,"type":20},120,[23],"The goal of this clinical trial is to test a digital treatment for patients with subacromial pain using the digital Shoulder Aid (diSAID) strategy. The participants in this study will be randomly assigned to digital treatment (diSAID) or to receive the treatment that is currently available in primary care, i.e. continue according to usual practice.\n\nThe main question this clinical trial aims to answer are:\n\n\\- Can the diSAID improve shoulder function and reduce pain for patients with subacromial pain in primary care?",[26,280,307],"Rotator Cuff Syndrome",[112,309,310,311,312,313],"Subacromial pain","Digital care","Digital health intervention","Physiotherapy","Primary care","2024-02-18",{"date":316,"type":36},"2024-02-23",{"date":318,"type":20},"2024-02-26",{"date":320,"type":20},"2028-03-26",{"name":322,"class":43},"Region Östergötland"]