[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"shoulder-tendinopathy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:shoulder-tendinopathy":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,45,77,105,131],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100639307","immersive-virtual-reality-versus-conventional-physiotherapy-for-shoulder-tendinopathy-100639307",false,"NCT07592156","Immersive Virtual Reality Versus Conventional Physiotherapy for Shoulder Tendinopathy","Efficacy of Immersive Virtual Reality Compared With Conventional Physiotherapy in the Management of Shoulder Tendinopathy: A Randomized Controlled Pilot Study","HOMVR","Inclusion Criteria:\n\n* Confirmed diagnosis of shoulder tendinopathy.\n* Referral to the shoulder rehabilitation program.\n* Age between 18 and 80 years.\n* Willingness to use immersive virtual reality headsets.\n* Ability to understand the study procedures and provide written informed consent.\n\nExclusion Criteria:\n\n* Acute or exacerbated phase of shoulder tendinopathy, defined as resting pain greater than 7 points on a 0-to-10 Numeric Rating Scale.\n* Simultaneous participation in another clinical study.\n* Current physiotherapy treatment for the same shoulder condition.\n* Recent infiltrative treatment within the previous 3 months.\n* Any condition contraindicating the use of immersive virtual reality, including photosensitive epilepsy, severe vertigo, claustrophobia, or active ocular or facial infections.\n* Intolerance to the use of virtual reality headsets.","ALL","18 Years","80 Years",{"count":21,"type":22},20,"ESTIMATED","INTERVENTIONAL",[25],"NA","Immersive virtual reality (VR) has emerged as a promising tool to support therapeutic exercise by increasing patient motivation, promoting movement through gamification, and potentially reducing pain perception during movement. However, evidence regarding its use in shoulder tendinopathy remains limited.\n\nThis randomized controlled pilot study will evaluate the clinical efficacy and feasibility of an immersive VR-based exercise program compared with conventional physiotherapy in patients with shoulder tendinopathy. A total of 20 patients referred to the Rehabilitation Department of Hospital Universitario de La Línea de la Concepción will be randomly allocated to either a conventional therapeutic exercise group or an immersive VR-based exercise group. Both interventions will last 4 weeks, with 3 sessions per week, for a total of 12 sessions.\n\nThe primary outcome will be shoulder pain and disability measured with the Shoulder Pain and Disability Index (SPADI). Secondary outcomes will include pain intensity, upper limb function, shoulder range of motion, isometric strength, kinesiophobia, and patient satisfaction. Outcomes will be assessed at baseline and immediately after the 4-week intervention",[28],"Shoulder Tendinopathy",[30,31],"rotator cuff tendinopathy","shoulder pain","NOT_YET_RECRUITING","2026-05-11",{"date":35,"type":36},"2026-05-18","ACTUAL",{"date":38,"type":22},"2026-05-01",{"date":40,"type":22},"2026-12-01",{"name":42,"class":43},"Universidad de Burgos","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":23,"phases":55,"briefSummary":56,"conditions":57,"keywords":58,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":44},"100635273","pemf-therapy-in-shoulder-tendinopathy-100635273","NCT07550543","PEMF Therapy in Shoulder Tendinopathy","Effect of Pulsed Electromagnetic Field (PEMF) Therapy Delivered Via the Super Inductive System (SIS) Combined With Balneophysiotherapy in Patients With Shoulder Tendinopathies: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Adults aged between 18 and 70 years.\n* Patients with chronic shoulder pain lasting more than 3 months, of non-traumatic origin, persistent despite prior conservative treatment.\n* Clinical diagnosis of shoulder tendinopathy and\u002For subacromial pain syndrome based on medical history and physical examination.\n* Presence of shoulder pain and functional limitation confirmed by clinical assessment and baseline functional evaluation (SPADI).\n* Ability to comply with the treatment protocol and attend scheduled follow-up assessments.\n* Provision of written informed consent prior to participation.\n\nExclusion Criteria:\n\n* Full-thickness rotator cuff tears with surgical indication.\n* Recent major shoulder trauma (within the last 6 months).\n* Active systemic inflammatory or rheumatologic diseases.\n* Presence of metallic implants in the treatment area or implanted electronic devices (e.g., pacemaker).\n* Neurological disorders affecting the upper limb.\n* Contraindications to balneotherapy (e.g., severe cardiovascular disease, renal failure, severe dermatological conditions).\n* Decompensated chronic diseases at the time of enrollment (cardiovascular, hepatic, renal, respiratory, or neurological).\n* Skin lesions at the site of treatment application.\n* Pregnancy or breastfeeding.\n* Active neoplastic disease.\n* Decompensated psychiatric disorders.\n* History of hypersensitivity to natural therapeutic factors used in balneotherapy.\n* Refusal to participate or inability to provide informed consent.","70 Years",{"count":54,"type":22},60,[25],"The goal of this clinical trial is to evaluate whether pulsed electromagnetic field (PEMF) therapy delivered via the Super Inductive System (SIS), integrated into a multimodal rehabilitation program, improves pain, function, pressure pain threshold, muscle strength, psychological status, and quality of life in adults with shoulder tendinopathies.\n\nThe main questions it aims to answer are:\n\n* Does the addition of PEMF (SIS) therapy reduce pain intensity and improve pressure pain threshold compared to standard balneophysiotherapy?\n* Does PEMF (SIS) therapy improve shoulder function, muscle strength, psychological status, and quality of life? The study will compare a multimodal rehabilitation program supplemented with PEMF (SIS) therapy to standard balneophysiotherapy to determine whether the addition of PEMF (SIS) provides superior clinical outcomes.\n\nParticipants will:\n\n* Undergo a multimodal rehabilitation program including balneophysiotherapy\n* Be assigned to receive either standard treatment or treatment supplemented with PEMF (SIS) therapy\n* Be evaluated at baseline (admission), immediately after treatment completion (discharge), and at 4 weeks after treatment using validated clinical instruments assessing pain, function, pressure pain threshold, muscle strength, psychological status, depressive symptoms, and quality of life.",[28],[59,60,61,62,63,64,65,66],"Nanopulsed Electromagnetic Field","Pulsed Electromagnetic Field","PEMF","Super Inductive System","Balneotherapy","Physiotherapy","Shoulder Pain","Tendinopathy","RECRUITING","2026-04-20",{"date":70,"type":36},"2026-04-24",{"date":72,"type":36},"2026-04-01",{"date":74,"type":22},"2026-08",{"name":76,"class":43},"Balnear and Rehabilitation Sanatorium Techirghiol",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":83,"enrollmentInfo":84,"targetDuration":4,"studyType":23,"phases":86,"briefSummary":87,"conditions":88,"keywords":93,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"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":85,"type":22},46,[25],"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",[89,90,91,28,92],"Rotator Cuff Related Shoulder Pain","Subacromial Pain Syndrome","Shoulder Bursitis","Rotator Cuff Tears of the Shoulder",[94,95,96],"Rotator cuff","Shoulder pain","attention shift",{"date":98,"type":36},"2026-04-22",{"date":100,"type":22},"2026-05-15",{"date":102,"type":22},"2027-06-15",{"name":104,"class":43},"Istanbul University",{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":110,"acronym":4,"eligibilityCriteria":111,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":52,"enrollmentInfo":112,"targetDuration":4,"studyType":23,"phases":114,"briefSummary":115,"conditions":116,"keywords":118,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":130},"100634907","electroacupuncture-and-cupping-for-shoulder-tendinitis-100634907","NCT07545785","Electroacupuncture and Cupping for Shoulder Tendinitis","Effectiveness of Electroacupuncture Combined With Cupping Therapy in Patients With Shoulder Tendinitis and qi Stagnation and Blood Stasis Syndrome","Inclusion Criteria:\n\n* Patients between 18 and 70 years old.\n* Pain intensity score on the Visual Analogue Scale (VAS) between 4 and 7.\n* Diagnosis of rotator cuff and\u002For long head of the biceps tendonitis according to the guidelines issued by the Ministry of Health of Vietnam.\n* Mechanical pain that increases during movements such as abduction or raising the arm.\n* Presence of tender points at the long head of the biceps tendon or supraspinatus tendon .\n* Pain that increases during resisted contraction tests, such as the Jobe test or Palm-up test.\n* Absence of limitation in the passive range of motion of the shoulder.\n* Ultrasound findings showing a hypoechoic tendon or evidence of calcification.\n* Absence of motor weakness or paralysis.\n* Diagnosis of the TCM syndrome \"Qi Stagnation and Blood Stasis\"\n\nExclusion Criteria:\n\n* Patients who do not agree to participate in the study.\n* Diagnosis of pseudo-paralysis, acute calcific periarthritis, or frozen shoulder.\n* Shoulder pain caused by cervical nerve root lesions.\n* Shoulder pain originating from apical lung tumors, coronary artery disease, or myocardial infarction.\n* Specific joint lesions caused by infection, tuberculosis, or rheumatoid arthritis.\n* Bone pathologies including fractures, dislocations, or osteonecrosis of the humeral head.\n* Shoulder dysfunction resulting from stroke or hemiplegia.\n* Women who are pregnant.\n* Patients with mental illness.\n* Contraindications for vacuum cupping, such as acute skin inflammation, open wounds, or alcohol consumption.\n* Contraindications for electroacupuncture, including cardiac pacemakers, heart failure, or local skin ulcers.\n* Current participation in another intervention study.\n* Use of painkillers, muscle relaxants, or within the last week.\n* Use of anticoagulants or a history of hemophilia.",{"count":113,"type":22},54,[25],"This study aims to evaluate the effectiveness of electroacupuncture combined with vacuum cupping therapy in treating simple periarthritis of the shoulder associated with the traditional medicine syndrome of Qi stagnation and blood stasis. Shoulder periarthritis is a common condition that causes pain, stiffness, and limited movement of the shoulder due to injury or inflammation of the muscles, tendons, ligaments, and surrounding soft tissues. It can interfere with daily activities such as dressing, lifting objects, sleeping, and working.\n\nElectroacupuncture is commonly used to relieve shoulder pain and improve shoulder function. Vacuum cupping therapy is another non-drug treatment that may help improve blood circulation, reduce muscle tightness, decrease pain, and improve mobility. However, there is currently limited evidence about whether combining electroacupuncture with vacuum cupping provides better results than electroacupuncture alone in patients with shoulder periarthritis and Qi stagnation-blood stasis syndrome. This study is being conducted to determine whether the combined treatment is more effective and safe.\n\nA total of 54 participants with simple shoulder periarthritis and Qi stagnation-blood stasis syndrome will be enrolled in the study. Participants will be randomly assigned to one of two groups:\n\nGroup 1: treatment with electroacupuncture alone. Group 2: treatment with electroacupuncture combined with vacuum cupping therapy.\n\nAll participants will also receive advice on shoulder exercises, posture, and daily activities to support recovery. Treatments will be performed by licensed traditional medicine practitioners.\n\nEach participant will take part in the study for two weeks. Assessments will be performed before treatment, after one week, and after two weeks. The study will evaluate:\n\nPain intensity using the Visual Analogue Scale (VAS). Shoulder pain and disability using the Shoulder Pain and Disability Index (SPADI).\n\nShoulder range of motion using the McGill-McRomi Range of Motion Index. Any side effects or unwanted events related to treatment. Possible benefits of participating in this study include reduced shoulder pain, improved movement and daily function, and close monitoring by health care professionals. Participants may also benefit from receiving non-drug therapies at no cost during the study period. The findings of this research may help improve future treatment options for patients with shoulder pain.\n\nPossible risks of electroacupuncture include mild pain at the needle site, minor bleeding, bruising, dizziness, or fainting. Possible risks of vacuum cupping include temporary discomfort, skin redness, bruising, or mild pain in the treated area. These side effects are usually mild and temporary. If any unexpected problem occurs, participants will receive prompt medical attention.\n\nParticipation in this study is completely voluntary. Participants may refuse to join or may withdraw from the study at any time without affecting their usual medical care. All personal information collected during the study will remain confidential and will only be used for research purposes.",[28,117],"Shoulder Tendinitis",[119,120,121,117],"shoulder tendinopathy","Rotator cuff tendinitis","Long head of the biceps tendonitis","2026-04-16",{"date":98,"type":36},{"date":125,"type":36},"2026-03-01",{"date":127,"type":22},"2026-11-15",{"name":129,"class":43},"University of Medicine and Pharmacy at Ho Chi Minh City",2,{"id":132,"slug":133,"hasResults":11,"nctId":134,"briefTitle":135,"officialTitle":136,"acronym":137,"eligibilityCriteria":138,"healthyVolunteers":139,"sex":17,"minAge":18,"maxAge":52,"enrollmentInfo":140,"targetDuration":4,"studyType":142,"phases":4,"briefSummary":143,"conditions":144,"keywords":146,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":151,"lastUpdatePostDateStruct":152,"startDateStruct":154,"completionDateStruct":156,"leadSponsor":158,"locationsCount":44},"100557320","nutrition-impact-on-prgf-treatment-for-tendinopathy-100557320","NCT06536582","Nutrition Impact on PRGF Treatment for Tendinopathy","Nutrition as a Risk Factor and Predictor of Treatment Outcome With Plasma Rich Growth Factors for Shoulder Tendinopathy","NUTRITENDON","Inclusion Criteria:\n\n* Male and female\n* Age ≥18 years and ≤ 70 years\n* Patients presenting shoulder tendinopathy\n* Signing of the Informed Consent of the Regain observational study\n* Signature of informed consent of the present study.\n\nExclusion Criteria:\n\n* Pregnancy (ascertained by self-declaration), breastfeeding\n* Inability to follow the study protocol\n* Heart, kidney, oncological disease\n* Neuropsychiatric disease\n* Other conditions that, at the discretion of the investigator or physician, exclude enrollement",true,{"count":141,"type":22},52,"OBSERVATIONAL","Given the close correlation reported in the literature between onset and progression of tendon pathology in subjects affected by the alteration of metabolic disorders such as obesity, diabetes mellitus and lipidic metabolic alterations, with the present study the association between the nutritional state, metabolic profile and clinical outcome of patients following treatment with blood-derived orthobiological for shoulder tendinopathies will be evaluated.\n\nThe primary aim of this study is to identify the proportion of tendinopatic patients responsive and non-responsive to treatment with \"Platelet rich growth factors\" PRGF at six months follow up and the correlation with their nutritional status.",[28,145],"Metabolic Alterations",[147,148,149,150],"nutritional status","responder and non-responder patients","orthobiologics","Platelet rich growth factors","2024-07-30",{"date":153,"type":36},"2024-08-05",{"date":155,"type":36},"2024-02-15",{"date":157,"type":22},"2027-02-15",{"name":159,"class":43},"I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio"]