[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"adhesive-capsulitis-of-the-shoulder\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:adhesive-capsulitis-of-the-shoulder":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,44,72,98,125,149,175,198,221],{"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":29,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100631212","phase-4-omt-for-adhesive-capsulitis-100631212",false,"NCT07497737","OMT for Adhesive Capsulitis","Osteopathic Manipulative Treatment as an Adjunct Therapy for Adhesive Capsulitis","Inclusion Criteria:\n\n* patients diagnosed with adhesive capsulitis who have not received prior treatment for it\n\nExclusion Criteria:\n\n* patients with contraindications to corticosteroid injections (uncontrolled diabetes, active infection, bleeding disorders, or corticosteroid hypersensitivity)\n* patients diagnosed with adhesive capsulitis who have received (or are currently receiving) treatment for it","ALL","18 Years","89 Years",{"count":20,"type":21},300,"ESTIMATED","INTERVENTIONAL",[24],"PHASE4","The goal of this clinical trial is to learn if Osteopathic Manipulative Treatment (OMT) is an effective addition to treatment of adhesive capsulitis. OMT is a non-invasive treatment in which a doctor gently moves and stretches muscles, joints, and tissues manually. Adhesive capsulitis is more commonly known as \"frozen shoulder\" and describes a shoulder that becomes stiff, painful, and limited in its motion due to some structural change in the joint. The main questions it aims to answer are:\n\nIs recovery faster when OMT is added to regular treatment? Are patients that underwent OMT more satisfied with their treatment?\n\nResearchers will compare patients who underwent OMT to patients who did not to see if OMT is an effective additional treatment for frozen shoulder.\n\nParticipants will:\n\n* Be assigned to one of the four experimental groups\n* Visit clinic and\u002For physical therapy to undergo the treatments associated with their group:\n\n  1. standard course of prescribed physical therapy\n  2. standard course of prescribed physical therapy and an injection of an anti-inflammatory and anesthetics in the shoulder\n  3. standard course of prescribed physical therapy and (up to) 4 OMT sessions\n  4. standard course of prescribed physical therapy, an injection of an anti-inflammatory and anesthetics in the shoulder, and (up to) 4 OMT sessions.\n* Visit clinic 1 month, 3 months, 6 months, and 1 year after treatment is complete\n* Complete a survey about how satisfied they are with their treatment 1 month, 3 months, 6 months, and 1 year after it is complete",[27,28],"Adhesive Capsulitis of the Shoulder","Frozen Shoulder",[30,27,28],"Osteopathic Manipulative Treatment (OMT)","NOT_YET_RECRUITING","2026-06-08",{"date":34,"type":35},"2026-06-09","ACTUAL",{"date":37,"type":21},"2026-08-01",{"date":39,"type":21},"2028-05-01",{"name":41,"class":42},"University Hospitals Cleveland Medical Center","OTHER",3,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":52,"minAge":53,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":59,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":71},"100614340","phase-4-frozen-shoulder-and-hormone-replacement-therapy-100614340","NCT07278323","Frozen Shoulder and Hormone Replacement Therapy","Hormone Replacement Therapy as an Adjunct Treatment for Adhesive Capsulitis of the Shoulder (Frozen Shoulder) in Peri- and Postmenopausal Women","FSHRT","Inclusion Criteria:\n\n* Diagnosis of adhesive capsulitis of the shoulder\n\nExclusion Criteria:\n\n* History of hormone sensitive cancer\n* Bilateral adhesive capsulitis of the shoulder\n* Currently using hormonal treatments including contraceptives","FEMALE","40 Years",{"count":55,"type":21},60,[24],"The purpose of this study is to determine the effects of hormone replacement therapy (HRT) in addition to standard treatment on frozen shoulder symptoms in women with age-related changes to their menstrual cycle. Frozen shoulder refers to the condition a doctor diagnosed the participant with regarding shoulder pain, stiffness, and progressive loss of range of motion. Age-related menstrual cycle changes, known as perimenopause and\u002For menopause, refers to a change or stoppage of monthly menstrual cycles. Other symptoms participants may be experiencing include vaginal dryness, hot flashes, or night sweats. Hormone replacement therapy (HRT) refers to medicine with female hormones in it. For this study, HRT will be in the form of a patch that goes on the skin and a daily oral pill. Participants will be randomly assigned to receive either HRT plus standard care, or only standard care. Follow-up tests will be completed at 6 months of treatment to assess participant progress.",[27,28],[28,60,61],"Hormone Replacement Therapy","Perimenopause","RECRUITING","2026-06-04",{"date":32,"type":35},{"date":66,"type":35},"2026-01-15",{"date":68,"type":21},"2026-12",{"name":70,"class":42},"University of California, San Francisco",1,{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":16,"minAge":80,"maxAge":81,"enrollmentInfo":82,"targetDuration":4,"studyType":22,"phases":84,"briefSummary":86,"conditions":87,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":92,"completionDateStruct":94,"leadSponsor":96,"locationsCount":71},"100618840","transcatheter-arterial-embolization-using-nexsphere-f-for-chronic-shoulder-pain-refractory-to-conservative-treatment-100618840","NCT07336849","Transcatheter Arterial Embolization Using Nexsphere-F for Chronic Shoulder Pain Refractory to Conservative Treatment","A Single-center, Prospective, Open Label Randomized Clinical Trial to Evaluate the Efficacy and Safety of Transcatheter Arterial Embolization Using 'Nexsphere-F' in Patients With Adhesive Capsulitis of the Shoulder Joint Refractory to Conservative Treatment.","TAE-FROST","Inclusion Criteria:\n\n* Patients who have voluntarily signed a written informed consent form after receiving an explanation of the purpose, methods, and potential effects of the clinical trial\n\n  * Patients aged between 19 and 85 years\n\n    * Patients with pain persisting for more than 3 months in the affected area and with a history of receiving physical therapy, analgesics\u002Fanti-inflammatory medications, or local injection treatments\n\n      * Patients with a measured shoulder joint range of motion (ROM) of less than 90 degrees ⑤ Patients who agree not to receive any conservative treatment other than those permitted in this clinical trial (physical therapy, medication \\[NSAIDs, opioid analgesics, acetaminophen\\], intra-articular injections such as hyaluronic acid)\n\n        * Patients who are willing to comply with the treatment and procedures of the clinical trial and participate in all follow-up evaluations through hospital visits or telephone surveys\n\nExclusion Criteria:\n\n* Patients with a history of surgery on the shoulder joint targeted for the clinical trial prior to screening\n\n  * Patients suspected of having a full-thickness rotator cuff tear\n\n    * Patients with bleeding disorders or coagulopathies (e.g., idiopathic thrombocytopenic purpura, hemophilia, disseminated intravascular coagulation)\n\n      * Patients with advanced atherosclerosis or vasospasm in the arm vessels, or those expected to have such conditions\n\n        * Patients with a known hypersensitivity to gelatin\n\n          ⑥ Patients with a known hypersensitivity to contrast media\n\n          ⑦ Patients who are pregnant or breastfeeding\n\n          ⑧ Patients with a localized infection at the pain site\n\n          ⑨ Patients deemed inappropriate for participation by the investigator due to ethical concerns or potential impact on the clinical trial results","19 Years","85 Years",{"count":83,"type":21},44,[85],"NA","Evaluation of the efficacy and safety of transcatheter arterial embolization using 'Nexsphere-F' for pain relief in patients with adhesive capsulitis of the shoulder joint that does not respond to conservative treatment.\n\nThis study aims to investigate the efficacy and safety of transcatheter arterial embolization using embolic agents in patients with adhesive capsulitis of the shoulder joint. This is a single-center, prospective, open-label, randomized clinical trial.",[27,28,88],"Shoulder Adhesive Capsulitis","2026-05-18",{"date":91,"type":35},"2026-05-19",{"date":93,"type":35},"2025-09-18",{"date":95,"type":21},"2027-08-31",{"name":97,"class":42},"Chung-Ang University Hosptial, Chung-Ang University College of Medicine",{"id":99,"slug":100,"hasResults":11,"nctId":101,"briefTitle":102,"officialTitle":102,"acronym":4,"eligibilityCriteria":103,"healthyVolunteers":11,"sex":16,"minAge":104,"maxAge":4,"enrollmentInfo":105,"targetDuration":4,"studyType":22,"phases":107,"briefSummary":108,"conditions":109,"keywords":110,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":71},"100630016","effectiveness-and-efficiency-of-an-upper-limb-active-passive-exoskeleton-robot-in-patients-with-frozen-shoulder-100630016","NCT07482189","Effectiveness and Efficiency of an Upper Limb Active-Passive Exoskeleton Robot in Patients With Frozen Shoulder","Inclusion Criteria:\n\n\\-\n\n1\\. Patients aged 20 years or older diagnosed by a clinician with primary or secondary frozen shoulder or adhesive capsulitis:\n\n1. Patients diagnosed by a clinician with frozen shoulder or adhesive capsulitis in the stiff phase.\n2. The patient has a loss of at least 50% of passive joint range of motion (including of shoulder flexion, abduction, internal rotation, and external rotation) on the affected shoulder compared to the relatively healthy shoulder.\n\nExclusion Criteria:\n\n1. Individuals with osteoarthritis or other skeletal conditions of the shoulder joint.\n2. Individuals with any contraindications to treatment, such as joint fusion, severe osteoporosis, or symptoms of any peripheral nerve compression.\n3. Individuals with untreated joint dislocations, fractures, or tendon ruptures.\n4. Individuals who have received steroid injections within the month prior to the study.\n5. Individuals who are uncommunicated or cognitively impaired.\n6. Pregnant women.\n7. Patients who refuse recruitment will also be excluded.","20 Years",{"count":106,"type":21},40,[85],"Frozen shoulder, also known as adhesive capsulitis, is a common chronic shoulder disorder with symptoms including shoulder pain, limitations in both active and passive range of motion, and muscle weakness, which significantly affects daily functional abilities. The investigator applied upper limb exoskeleton-assisted therapy. This experiment used a randomized controlled trial to assess the clinical rehabilitation effects of exoskeleton-assisted range of motion and resistance training on patients with frozen shoulder.",[27,28],[111,112,113,114,115],"Frozen shoulder","Adhesive capsulitis","Exoskeleton robots","Robot-assisted rehabilitation","Rehabilitation","2026-03-21",{"date":118,"type":35},"2026-03-25",{"date":120,"type":21},"2026-03-16",{"date":122,"type":21},"2027-03-15",{"name":124,"class":42},"China Medical University Hospital",{"id":126,"slug":127,"hasResults":11,"nctId":128,"briefTitle":129,"officialTitle":130,"acronym":4,"eligibilityCriteria":131,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":132,"enrollmentInfo":133,"targetDuration":4,"studyType":22,"phases":135,"briefSummary":136,"conditions":137,"keywords":138,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":143,"startDateStruct":144,"completionDateStruct":146,"leadSponsor":147,"locationsCount":71},"100624449","capsular-distension-versus-corticosteroid-injection-in-adhesive-capsulitis-100624449","NCT07409779","Capsular Distension Versus Corticosteroid Injection in Adhesive Capsulitis","Capsular Distension Versus Corticosteroid Injection in Patients With Adhesive Capsulitis: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Age between 18 and 80 years\n* Ability to provide informed consent\n* Shoulder pain with Visual Analog Scale (VAS) ≥ 40\u002F100\n* Limitation of external rotation \\\u003C 45° or \\\u003C 50% compared to the contralateral side\n* Clinically diagnosed adhesive capsulitis with normal shoulder radiography\n\nExclusion Criteria:\n\n* Rotator cuff tear\n* Previous shoulder surgery\n* Cervico-brachial neuralgia\n* Pregnancy or breastfeeding\n* Poorly controlled diabetes\n* Coagulation disorders or anticoagulant therapy with INR \\> 3\n* Allergy to lidocaine\n* Inflammatory rheumatic diseases\n* Severe cardiovascular or hematological diseases\n* Active infection or immunodeficiency\n* Severe psychiatric disorders\n* Recent shoulder rehabilitation (within 1 week)\n* Intra-articular corticosteroid injection or hyaluronic acid injection within the last 6 months\n* Refusal to sign informed consent","80 Years",{"count":134,"type":21},50,[85],"Adhesive capsulitis is a common and disabling shoulder condition characterized by pain and progressive limitation of range of motion. Capsular distension and intra-articular corticosteroid injection are commonly used therapeutic options, often combined with rehabilitation, but their comparative effectiveness remains debated.\n\nThe objective of this randomized controlled trial is to compare the efficacy and tolerance of ultrasound-guided capsular distension combined with rehabilitation versus intra-articular corticosteroid injection combined with rehabilitation in patients with adhesive capsulitis.\n\nOutcomes will include shoulder pain, range of motion, functional disability, patient satisfaction, and procedure-related complications, assessed at short, mid, and long-term follow-up.",[27],[139,140,141,142],"adhesive capsulitis","capsular distension","rehabilitation","corticosteroid",{"date":118,"type":35},{"date":145,"type":21},"2026-04-01",{"date":68,"type":21},{"name":148,"class":42},"Faculty of Medicine of Tunis",{"id":150,"slug":151,"hasResults":11,"nctId":152,"briefTitle":153,"officialTitle":154,"acronym":4,"eligibilityCriteria":155,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":156,"enrollmentInfo":157,"targetDuration":4,"studyType":22,"phases":159,"briefSummary":160,"conditions":161,"keywords":163,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":167,"startDateStruct":169,"completionDateStruct":171,"leadSponsor":173,"locationsCount":4},"100620946","anterior-vs-posterior-vs-combined-intra-articular-injections-for-adhesive-capsulitis-100620946","NCT07364227","Anterior vs Posterior vs Combined Intra-Articular Injections for Adhesive Capsulitis","Comparison of Anterior, Posterior, and Combined Intra-Articular Injection Techniques in Patients With Adhesive Capsulitis","Inclusion Criteria Age 18-70 years Unilateral shoulder pain and stiffness (symptom duration 1-9 months) NRS pain score ≥ 7\u002F10 Passive range of motion limitation \\>50% in at least two planes, or \\>30° restriction in ≥2 planes \"Freezing stage\" (stage 2 adhesive capsulitis) No analgesic use (NSAIDs, opioids, acetaminophen) within 12 hours before intervention Radiography and\u002For MRI excluding other pathologies (rotator cuff tear, labral lesion, osteoarthritis, etc.) Exclusion Criteria Secondary adhesive capsulitis (trauma, surgery, systemic disease) Prior shoulder surgery or intra-articular steroid injection within 3 months Bilateral frozen shoulder Neurological disorders (Parkinson's disease, ALS, neuropathies) Malignancy, infection, cellulitis, septic arthritis, acute fracture Cognitive impairment, psychiatric disorders, pregnancy Steroid or local anesthetic allergy Poor glycemic control or other contraindications to steroid injections","70 Years",{"count":158,"type":21},30,[85],"This randomized controlled clinical trial aims to compare the efficacy of three different intra-articular injection approaches (anterior, posterior, and combined anterior-posterior) in patients with adhesive capsulitis of the shoulder. Thirty participants will be randomly assigned to one of three groups and treated with a standardized injection solution consisting of corticosteroid, lidocaine, and saline. Clinical outcomes will be evaluated using pain scores, functional scales, and imaging parameters.",[27,162],"Intra Articular Injection",[27,164,28,165,166],"Intra-articular Injection","Ultrasound","Shoulder Pain",{"date":168,"type":35},"2026-01-23",{"date":170,"type":21},"2026-01",{"date":172,"type":21},"2026-07",{"name":174,"class":42},"Aslinur Keles Ercisli, MD, PhD",{"id":176,"slug":177,"hasResults":11,"nctId":178,"briefTitle":179,"officialTitle":180,"acronym":4,"eligibilityCriteria":181,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":182,"targetDuration":4,"studyType":22,"phases":183,"briefSummary":185,"conditions":186,"keywords":187,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":189,"lastUpdatePostDateStruct":190,"startDateStruct":192,"completionDateStruct":194,"leadSponsor":196,"locationsCount":71},"100581289","phase-3-dose-efficacy-in-adhesive-capsulitis-100581289","NCT06848374","Dose Efficacy in Adhesive Capsulitis","Dose Comparison for the Treatment of Adhesive Capsulitis with Hydrodilatation and Corticosteroid Using an Anterior Approach Under Ultrasound-Guidance","Inclusion Criteria:\n\n* \\>18 years of age\n* Diagnostic of adhesive capsulitis of the shoulder\n\nExclusion Criteria:\n\n* Injection received in the affected shoulder \\\u003C 3 months ago (any kind)\n* History of previous surgery in the affected shoulder\n* Glenohumeral osteoarthritis more than mild on the xray\n* Pregnancy\n* Blood thinner (other than Aspirin 80 mg) or bleeding disorder\n* Active infection (requiring antibiotic)\n* Allergy to steroid or lidocaine\n* Cognitive impairment\n* Active litigation\n* Inflammatory connective tissue disorder",{"count":106,"type":21},[184],"PHASE3","The purpose of this study is to find out if the treatment of adhesive capsulitis with 40 mg of methylprednisolone in combination with a hydrodilatation is comparable to 80 mg of methylprednisolone for pain reduction, improving shoulder mobility, and reducing side effects.\n\nResearchers will enroll 40 people in this study which is taking place solely at the Toronto Rehabilitation Institute, University Avenue. This study should take approximately 12 months to complete and the results should be known in about 15 to 18 months. During this study, patients will receive an ultrasound guided shoulder hydrodilatation combined with corticosteroid after \"randomized\" into one of the groups (40 mg vs 80 mg). This is a double blind study as both patients and physicians would not know the group patient was randomized to.\n\nPain scores, Range of Motion and few other questionnaires wold be completed to track the response to the interventions at baseline prior to injection, four weeks after the procedure and 3 months after the procedure.",[27],[111,188],"hydrodilatation","2025-02-23",{"date":191,"type":35},"2025-02-27",{"date":193,"type":35},"2024-12-20",{"date":195,"type":21},"2026-12-31",{"name":197,"class":42},"University Health Network, Toronto",{"id":199,"slug":200,"hasResults":11,"nctId":201,"briefTitle":202,"officialTitle":203,"acronym":4,"eligibilityCriteria":204,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":205,"targetDuration":4,"studyType":22,"phases":207,"briefSummary":208,"conditions":209,"keywords":210,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":212,"lastUpdatePostDateStruct":213,"startDateStruct":215,"completionDateStruct":217,"leadSponsor":219,"locationsCount":71},"100574989","effectiveness-of-instrumental-rehabilitation-in-patients-with-adhesive-capsulitis-100574989","NCT06766448","Effectiveness of Instrumental Rehabilitation in Patients With Adhesive Capsulitis","Robotic Training in the Management of Adhesive Capsulitis: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients \\>18 years of age\n* Shoulder pain and\u002For movement limitation\n* Idiopathic AC or associated with confirmed systemic disease (e.g., diabetes or dyslipidemia)\n\nExclusion Criteria:\n\n* Cognitive impairment\n* History of surgery\n* Fracture or dislocation of the shoulder\n* History of shoulder tendinopathy\n* History of inflammatory or degenerative disease\n* Infection\n* Neurological disease (Parkinson's disease, stroke, multiple sclerosis, neurological\n* Manipulation under anesthesia, hydro dilation, platelet rich plasma or hyaluronic acid infiltration within the last 6 months",{"count":206,"type":21},70,[85],"The aim of this study is to evaluate the effectiveness of robotic training compared to conventional rehabilitation in patients with AC.",[27],[139,141,211],"robotic training","2025-01-30",{"date":214,"type":35},"2025-02-03",{"date":216,"type":35},"2021-03-23",{"date":218,"type":21},"2025-04",{"name":220,"class":42},"Mohammed V Souissi University",{"id":222,"slug":223,"hasResults":11,"nctId":224,"briefTitle":225,"officialTitle":226,"acronym":4,"eligibilityCriteria":227,"healthyVolunteers":228,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":229,"targetDuration":4,"studyType":22,"phases":230,"briefSummary":231,"conditions":232,"keywords":233,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":239,"lastUpdatePostDateStruct":240,"startDateStruct":242,"completionDateStruct":244,"leadSponsor":246,"locationsCount":71},"100577256","evaluation-and-treatment-of-adhesive-capsulitis-using-non-invasive-neurostimulation-devices-100577256","NCT06795932","Evaluation and Treatment of Adhesive Capsulitis Using Non-invasive Neurostimulation Devices","Prise En Charge Des Atteintes Proprioceptives Chez Une Population Avec Capsulite Rétractile","Inclusion Criteria:\n\n* 18 years old and over\n* Good general health\n* Adhesive capsulitis (experimental group) or\n* No shoulder pain (placebo group)\n\nExclusion Criteria:\n\n* Cognitive disorders;\n* Any neurological disease\u002Finjury affecting the upper limbs;\n* History or diagnosis of muscle, tendon, or capsular tear;\n* Shoulder surgery\u002Fprosthesis;\n* Pregnant woman;\n* Presence of metal in the skull or jaw;\n* History of epilepsy.",true,{"count":158,"type":21},[85],"The goal of this randomized controlled trial is to compare the integrity of somatosensory processing with transcranial magnetique stimulation (TMS) and corticospinal excitability of the affected shoulder in individuals with adhesive capsulitis versus healthy controls.\n\nThe secondary objective is to compare the clinical and neurophysiological effects of an intervention using tendon vibration (VIB) to induced kinesthetic illusions. This will involve comparing two groups: one receiving a real intervention versus a placebo intervention protocol, both coupled with standardized exercises in individuals with capsulitis. The hypotheses are that the proprioceptive processing and corticospinal excitability are impaired in the presence of capsulitis, and that the VIB + exercises intervention will result in greater improvements than the placebo VIB + exercises.\n\nTo goal is to establish the first empirical foundations for understanding adhesive capsulitis, using cutting-edge neurophysiological investigation technologies.\n\nTMS will be used to explore the presence of maladaptive plasticity in motor networks by assessing the excitability and integrity of the primary motor cortex (M1) and the corticospinal tract.\n\nRecruitement:\n\n30 healthy participants and 30 participants with a diagnosis of adhesive capsulitis will undergo 2 baselines assesments, 6 interventions with tendon vibration and 2 follow-up evaluation. Participants will be age- and sex-matched.\n\nBaseline and follw-up include:\n\n* Questionnaires : SPADI, QuickDASH, French version of the Mcgill Pain Questionnaire;\n* Active and passive range of motion;\n* Ultrasound for diagnosing capsulitis.\n\nComparison parameters:\n\n* active motor threshold (aMT)\n* Motor evoked potential (MEP) latency and amplitude\n* Standardized kinesthetic illusion procedure (SKIP) : direction of illusion, clearness, amplitude\u002Fspeed.\n\nInterventions :\n\n* 2 baselines including all questionnaires, ultrasound, active and passive range of motion, TMS procedure and SKIP;\n* 2 VIB interventions per week, for 3 weeks\n\n  * Real VIB : 80Hz of vibration to induce kinesthetic illusions,\n  * Placebo VIB : 40Hz of vibration that does not induce kinesthetic illusions\n* 2 follow-up including all questionnaires, ultrasound, active and passive range of motion, TMS procedure and SKIP.",[27,28],[234,111,235,236,237,238],"Adhesive Capsulitis","Tendon Vibration","Transcranial Magnetique Stimulation","Proprioception","Kinesthetic illusions","2025-01-27",{"date":241,"type":35},"2025-01-28",{"date":243,"type":35},"2024-10-17",{"date":245,"type":21},"2027-04",{"name":247,"class":42},"Université du Québec à Chicoutimi"]