[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"shoulder-arthroplasty\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:shoulder-arthroplasty":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,44,73,96,117,141,170,190,216],{"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":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100582901","early-versus-delayed-rehabilitation-after-reverse-total-shoulder-arthroplasty-for-proximal-humerus-fracture-100582901",false,"NCT06869343","Early Versus Delayed Rehabilitation After Reverse Total Shoulder Arthroplasty for Proximal Humerus Fracture","A Randomized Controlled Trial of Early Versus Delayed Rehabilitation After Reverse Total Shoulder Arthroplasty for Proximal Humerus Fracture","Inclusion Criteria:\n\n* aged 50-85 undergo reverse Total Shoulder Arthroplasty by a single surgeon for proximal humerus fractures\n\nExclusion Criteria:\n\n* previous rTSA to ipsilateral shoulder\n* undergoing elective rTSA\n* Prisoners\n* unwilling to be randomized\n* unwilling or unable to attend follow up visits","ALL","50 Years","85 Years",{"count":20,"type":21},10,"ESTIMATED","INTERVENTIONAL",[24],"NA","Proximal humerus fractures can be a debilitating injury in the elderly, impacting the ability to function independently or complete activities of daily living due to pain and restricted shoulder motion. Evidence has shown that reverse total shoulder arthroplasty (rTSA) is an effective option to improve pain and function for patients with acute displaced proximal humerus fractures. Given that patients undergoing rTSA for proximal humerus fractures typically experience worse functional outcomes, worse patient-reported outcomes, and higher rates of complication compared to those with elective indications for surgical intervention, it is critical to determine a secure path to recovery for these patients after surgery. Early rehabilitation has been proposed to be safe and effective for patients who undergo rTSA for elective indications; however, there is a paucity of research evaluating safety and effectiveness of timing of rehabilitation for rTSA patients in the trauma setting. Currently, there exists a great variability in postoperative rehabilitation protocols across orthopaedic practices. This study's objective is to determine the safety and effectiveness of early postoperative rehabilitation on the outcomes and postoperative complications of patients undergoing rTSA for proximal humerus fractures in order to provide more specific recommendations for this patient population.",[27,28,29,30],"Orthopedic Disorder","Humerus Fracture","Shoulder Arthroplasty","Reverse Shoulder Replacement","RECRUITING","2026-06-05",{"date":34,"type":35},"2026-06-09","ACTUAL",{"date":37,"type":35},"2025-05-19",{"date":39,"type":21},"2026-12-31",{"name":41,"class":42},"University of Virginia","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":4,"enrollmentInfo":52,"targetDuration":54,"studyType":55,"phases":4,"briefSummary":56,"conditions":57,"keywords":58,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":72},"100574043","shoulder-innovations-clinical-data-registry-100574043","NCT06754150","Shoulder Innovations Clinical Data Registry","SICDR","Inclusion Criteria:\n\n1. At least 18 years of age.\n2. Plan to receive or has received a shoulder arthroplasty surgical procedure, with a minimum of one implanted Shoulder Innovations (SI) device component and be willing and able to complete post-operative visits as long as at least one SI device component remains implanted.\n3. Able to provide informed consent prior to enrollment in the study (unless a waiver has been obtained).\n4. Agree to and be able to consistently answer the specified Patient Reported Outcome Measures (PROM) pre-operatively and at each of the post-operative visits without the use of a translator.\n5. Willing and able to comply with the requirements of the study protocol\n\nExclusion Criteria:\n\n1. Participation in a clinical trial of an investigational drug or device that would confound the results of this trial. Participation in another observational registry is allowed provided there are no conflicting requirements to this trial.\n2. Incarceration.\n3. Any conditions, co-morbidities, restrictions, or obligations that would prohibit them from complying with the requirements of this study protocol.","18 Years",{"count":53,"type":21},2500,"10 Years","OBSERVATIONAL","The goal of this multi-center observational study is to collect long-term clinical outcome information for anatomic and reverse total shoulder arthroplasty (shoulder replacement).",[29],[29,59,60,61],"Shoulder Replacement","Anatomic Shoulder Arthroplasty","Reverse Shoulder Arthroplasty","2026-05-08",{"date":64,"type":35},"2026-05-11",{"date":66,"type":35},"2024-10-23",{"date":68,"type":21},"2039-12",{"name":70,"class":71},"Shoulder Innovations","INDUSTRY",8,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":80,"enrollmentInfo":81,"targetDuration":4,"studyType":22,"phases":83,"briefSummary":85,"conditions":86,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":43},"100585465","phase-3-effects-of-oral-tranexamic-acid-on-short-term-postoperative-outcomes-following-total-shoulder-arthroplasty-100585465","NCT06902714","Effects of Oral Tranexamic Acid on Short Term Postoperative Outcomes Following Total Shoulder Arthroplasty","Evaluating the Effects of Oral Tranexamic Acid on Short Term Postoperative Outcomes Following Total Shoulder Arthroplasty: A Randomized Control Trial","Inclusion Criteria:\n\n* Skeletally mature patients (ages 18-79) undergoing primary total shoulder arthroplasty\n\nExclusion Criteria:\n\n* Patients with Cancer, venous thromboembolism, stroke, heart disease, pregnant or nursing, allergic to TXA, current tobacco use, anticoagulants other than aspirin.","79 Years",{"count":82,"type":21},60,[84],"PHASE3","The purpose of this clinical trial is to evaluate the short-term clinical outcomes of patients undergoing total shoulder arthroplasty who receive an extended postoperative course of oral tranexamic acid",[29],"2026-04-22",{"date":89,"type":35},"2026-04-28",{"date":91,"type":35},"2026-04-20",{"date":93,"type":21},"2030-12",{"name":95,"class":42},"University of Alabama at Birmingham",{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":101,"acronym":4,"eligibilityCriteria":102,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":4,"enrollmentInfo":103,"targetDuration":4,"studyType":55,"phases":4,"briefSummary":105,"conditions":106,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":107,"lastUpdatePostDateStruct":108,"startDateStruct":110,"completionDateStruct":112,"leadSponsor":114,"locationsCount":116},"100097298","hospital-for-special-surgery-shoulder-arthroplasty-cohort-100097298","NCT00527839","Hospital for Special Surgery Shoulder Arthroplasty Cohort","Prospective Evaluation of the Clinical and Economic Outcomes of Total Joint Replacement: HSS Shoulder Arthroplasty Cohort","Inclusion Criteria:\n\n* 18 years or older and undergoing total shoulder arthroplasty at HSS\n\nExclusion Criteria:\n\n* No other exclusion criteria. Pregnant women are eligible for the registry as this is a non-interventional study which only involves filling out questionnaires.",{"count":104,"type":21},250,"Total joint replacements are some of the most successful medical devices developed over the last fifty years. They enable millions of people to remain ambulatory and pain free, with minimal risk. In 2002, over 200,000 total hip replacements, 350,000 total knee replacements, and 25,000 total or partial shoulder replacements were performed in the United States (HCUP data). Future use will likely be even higher: it is estimated that by the year 2020, the population 65 and over in developed countries will increase by 71%. Existing studies do not provide adequate prospective data to evaluate long-term outcomes.\n\nHSS is a world leader in total joint replacement including total shoulder arthroplasty. However, there is no systematic follow-up or evaluation of patients who have their shoulders replaced here.\n\nThe purpose of this study is to establish a prospective cohort of HSS total shoulder arthroplasty to evaluate predictors of outcome, causes of failure and to allow ongoing evaluation of the results of our patients over time.",[29],"2026-02-11",{"date":109,"type":35},"2026-02-12",{"date":111,"type":4},"2007-04",{"date":113,"type":21},"2027-04",{"name":115,"class":42},"Hospital for Special Surgery, New York",2,{"id":118,"slug":119,"hasResults":11,"nctId":120,"briefTitle":121,"officialTitle":121,"acronym":122,"eligibilityCriteria":123,"healthyVolunteers":11,"sex":16,"minAge":124,"maxAge":4,"enrollmentInfo":125,"targetDuration":4,"studyType":22,"phases":126,"briefSummary":127,"conditions":128,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":132,"lastUpdatePostDateStruct":133,"startDateStruct":135,"completionDateStruct":137,"leadSponsor":139,"locationsCount":43},"100614666","role-of-nutritional-status-in-functional-recovery-of-older-adults-undergoing-virtual-reality-augmented-shoulder-rehabilitation-vir-100614666","NCT07282561","Role of Nutritional Status in Functional Recovery of Older Adults Undergoing Virtual Reality-augmented Shoulder Rehabilitation (VIR)","VIR","Inclusion Criteria:\n\n* Individuals aged 60 years old or older;\n* Frailty defined according to the Clinical Frailty Scale (Cesari et al., 2018);\n* Diagnosis of shoulder diseases with indication to elective surgery;\n\nExclusion Criteria:\n\n* Diagnosis of rheumatic diseases;\n* Shoulder fracture;\n* Actual SARS-CoV-2 infection;\n* Diagnosis of active cancer;\n* Any contraindication to oral feeding;\n* Malabsorptive diseases;\n* Cognitive impairment (MMSE\\\u003C18);\n* Severe chronic diseases (heart failure NYHA III-IV, lung failure, renal failure);\n* Any contraindication to rehabilitation;\n* Rehabilitation duration ≤ 14 days;\n* Inability to provide an informed consent;","60 Years",{"count":82,"type":21},[24],"Malnutrition is a clinical syndrome defined by involuntary weight loss and\u002For a persistent imbalance between nutritional needs and intake, leading to functional decline. Its prevalence is particularly high among older adults-affecting about 17% of community-dwelling elders, 30% of those in rehabilitation settings, and between 20% and 60% of individuals in acute care environments. Malnutrition is therefore a common yet often underrecognized factor influencing health outcomes in geriatric populations.\n\nOsteoarthritis (OA), a degenerative joint disease marked by the deterioration of articular cartilage, results in pain and reduced mobility. It affects approximately 9.6% of men and 18% of women over the age of 60. With global life expectancy rising and populations aging, OA is projected to become the fourth leading cause of disability by 2025. Joint replacement surgery provides significant relief for severe cases, and consequently, an increasing number of adults-averaging around 70 years of age-undergo elective joint replacement surgeries followed by rehabilitation for degenerative OA.\n\nIn this context, Virtual Reality (VR) technology is emerging as an innovative tool in rehabilitation. VR can create engaging, interactive environments that promote motor relearning by allowing clinicians to adjust practice intensity and provide real-time feedback. This adaptability enables personalized rehabilitation programs designed to enhance patient motivation and adherence. Preliminary studies have shown encouraging results, suggesting that VR-assisted therapy may improve motor recovery and functional outcomes, and its use in rehabilitation settings is rapidly expanding.\n\nPrevious research has identified a strong link between malnutrition and sarcopenia (loss of muscle mass) and reduced physical performance. However, findings remain inconsistent regarding how nutritional status influences functional recovery in elderly individuals undergoing rehabilitation. While some studies indicate a positive relationship between good nutrition and improved recovery, others suggest that nutritional status affects baseline functional capacity more than the rate or degree of functional improvement during rehabilitation.\n\nIt is also important to recognize that most available studies have focused on patients admitted for rehabilitation after hip fractures or stroke, conditions often associated with sudden functional decline. To date, only one known study has investigated elderly patients undergoing rehabilitation following hip or knee replacement surgery due to degenerative osteoarthritis. Interestingly, that study found a statistically significant positive association between nutritional status and functional recovery specifically in this subgroup-an association not observed among patients recovering from hip fractures or stroke.\n\nNonetheless, the study had limitations: nutritional status was measured using only the Mini Nutritional Assessment-Short Form (MNA-SF), and evaluation occurred post-surgery, without preoperative or long-term follow-up data. Moreover, there are no available data on rehabilitation outcomes for shoulder osteoarthritis, an increasingly common condition among older adults that significantly impacts autonomy in daily living.\n\nGiven these gaps, the current research aims to determine whether malnutrition modifies the effects of VR-enhanced shoulder rehabilitation after elective surgery on functional recovery-that is, the ability to perform activities of daily living (ADLs)-in frail elderly patients. The hypothesis is that poor nutritional status could reduce the benefits of intensive, technology-based rehabilitation, while adequate nutrition may enhance neuroplasticity, muscle strength, and overall recovery potential.\n\nThis investigation seeks to clarify three main aspects:\n\n1. The prevalence and severity of malnutrition among elderly individuals undergoing elective surgery and subsequent VR-based rehabilitation.\n2. The interaction between nutritional status and functional outcomes, examining whether malnutrition acts as an effect modifier or mediator in recovery trajectories.\n3. The specific contribution of VR technology in improving rehabilitation adherence, motivation, and overall functional independence compared to conventional therapy.\n\nBy exploring the intersection between nutrition, aging, and digital rehabilitation, this research could help tailor multidisciplinary interventions that integrate nutritional management and advanced rehabilitation technologies. Such an approach may optimize recovery outcomes, reduce disability, and improve quality of life in frail older adults undergoing joint replacement or shoulder surgery due to osteoarthritis.",[29,129,130,131],"Rehabilitation","Virtual Reality","Malnutrition Elderly","2025-12-01",{"date":134,"type":35},"2025-12-15",{"date":136,"type":35},"2025-11-01",{"date":138,"type":21},"2026-06-30",{"name":140,"class":42},"Claudio Pedone",{"id":142,"slug":143,"hasResults":11,"nctId":144,"briefTitle":145,"officialTitle":145,"acronym":146,"eligibilityCriteria":147,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":4,"enrollmentInfo":148,"targetDuration":4,"studyType":22,"phases":150,"briefSummary":152,"conditions":153,"keywords":156,"overallStatus":161,"whyStopped":4,"lastUpdateSubmitDate":162,"lastUpdatePostDateStruct":163,"startDateStruct":165,"completionDateStruct":167,"leadSponsor":169,"locationsCount":43},"100604220","phase-4-effect-of-local-anesthetic-concentration-on-rebound-pain-a-randomized-control-study-100604220","NCT07146685","Effect of Local Anesthetic Concentration on Rebound Pain: A Randomized Control Study","RPRCT","Inclusion Criteria:\n\n* Total shoulder replacement patients (anatomic and reverse)\n* Adult patients (greater than or equal to 18 years)\n* Any gender\n* Any race\n\nExclusion Criteria:\n\n* \\- Chronic Pain diagnoses including:\n* substance\u002Fopioid use disorder\n* complex regional pain syndromes\n* fibromyalgia\n* Daily persistent opioid use spanning 3 months prior to surgery date\n* Allergy to local anesthetics or NSAIDS\n* Respiratory pathologies including:\n* CPAP- non-compliant \u002F untreated obstructive sleep apnea\n* COPD\n* Restrictive lung disease (pulmonary fibrosis, interstitial pneumonia, etc)\n* Contralateral diaphragm dysfunction\n* BMI \\> 40\n* Ipsilateral extremity pre-existing nerve injury\n* GFR \\\u003C 60\n* NSAID contraindications\n* Inability to follow up\n* Revision surgery\n* Patients requesting block as primary (avoidance of general anesthesia)\n* Need or request for brachial plexus catheter or liposomal bupivacaine\n* Vulnerable populations (pregnancy, incarceration, etc)\n* non-English speaking",{"count":149,"type":21},168,[151],"PHASE4","Randomized control study that compares different concentrations of local anesthetic to investigate whether a lower concentration of local anesthetic would contribute to lower rebound pain scores at 24 hours post op in patients undergoing anatomic or reverse total shoulder arthroplasty.",[154,29,155],"Rebound Pain","Interscalene Block",[157,158,159,160],"local anesthetics","rebound pain","brachial plexus","shoulder arthroscopy","NOT_YET_RECRUITING","2025-08-20",{"date":164,"type":35},"2025-08-28",{"date":166,"type":21},"2026-01-01",{"date":168,"type":21},"2029-01-01",{"name":41,"class":42},{"id":171,"slug":172,"hasResults":11,"nctId":173,"briefTitle":174,"officialTitle":174,"acronym":4,"eligibilityCriteria":175,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":176,"enrollmentInfo":177,"targetDuration":54,"studyType":55,"phases":4,"briefSummary":178,"conditions":179,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":180,"lastUpdatePostDateStruct":181,"startDateStruct":183,"completionDateStruct":185,"leadSponsor":187,"locationsCount":189},"100325021","total-shoulder-arthroplasty-multi-center-registry-100325021","NCT03511586","Total Shoulder Arthroplasty Multi-Center Registry","Inclusion Criteria:\n\n1. Patient voluntarily consents to participate in the study and has the mental and physical ability to participate in the study, fill out subjective questionnaires, return for follow-up visits, and comply with prescribed post-operative physical therapy.\n2. Patient is between the ages of 18 and 100 years.\n3. The patient has a planned primary or revision implantation of an anatomic (hemi-arthroplasty or total arthroplasty) or a reverse shoulder prosthesis system manufactured by Arthrex.\n4. Patient has a standard of care preoperative CT taken within 6 months that has been submitted for Arthrex VIP (Virtual Implant Positioning) planning.\n\nExclusion Criteria\n\n1\\. Patient has known intentions, obligations, or co-morbidity that would inhibit them from participating in the study.","100 Years",{"count":53,"type":21},"The objective of the study is a multi-center prospective registry to collect clinical outcomes of anatomic and reverse total shoulder arthroplasty.",[29],"2025-08-06",{"date":182,"type":35},"2025-08-11",{"date":184,"type":35},"2015-07-28",{"date":186,"type":21},"2035-11",{"name":188,"class":71},"Arthrex, Inc.",24,{"id":191,"slug":192,"hasResults":11,"nctId":193,"briefTitle":194,"officialTitle":195,"acronym":4,"eligibilityCriteria":196,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":4,"enrollmentInfo":197,"targetDuration":4,"studyType":22,"phases":199,"briefSummary":200,"conditions":201,"keywords":203,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":207,"lastUpdatePostDateStruct":208,"startDateStruct":210,"completionDateStruct":212,"leadSponsor":214,"locationsCount":43},"100579986","post-incision-antimicrobial-wash-vs-c-acnes-in-shoulder-arthroplasty-100579986","NCT06831422","Post-incision Antimicrobial Wash vs C. Acnes in Shoulder Arthroplasty","Application of a Novel Antimicrobial Wash Versus Hydrogen Peroxide Versus Povidone-iodine to the Dermis and Incidence of Cutibacterium Acnes During Shoulder Arthroplasty: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Indicated and scheduled for primary shoulder arthroplasty.\n* Chronic severe glenohumeral osteoarthritis, avascular necrosis, post traumatic osteoarthritis, rotator cuff arthropathy,\n* Ability to read and understand English\n* Age ≥18 years\n* Patient failed ≥6 weeks of conservative treatment, which included non-steroidal anti-inflammatory drugs (NSAIDS)\n\nExclusion Criteria:\n\n* Patient with history of prior native shoulder septic arthritis or infection\n* Prior surgery of affected shoulder\n* Proximal Humerus Fracture\n* Active infection\n* Cancer\n* Autoimmune and rheumatologic disorders, including rheumatoid arthritis, psoriatic arthritis, systemic lupus erythematosus\n* History of allergic reaction to citric acid-derived products",{"count":198,"type":21},150,[24],"The purpose of this randomized controlled trial is to determine the effect of post-incision wash using various novel antimicrobial solutions on the rate of positive C. Acnes cultures collected from adults undergoing primary shoulder replacement surgery. Subjects will be randomly assigned in a 1:1:1:1 fashion to groups that will receive one of the following treatments:\n\n* Post-incision application of Xperience Antimicrobial wash (NextScience, Jacksonville, FL)\n* Post-incision application of 3% hydrogen peroxide\n* Post-incision application of 10% povidone-iodine (betadine)\n* No post-incision treatment (control)\n\nThe investigators hypothesize that the subjects treated with the antimicrobial solutions after initial incision will have lower rates of positive C. Acnes cultures. The investigators also hypothesize that post-incision application of Xperience Antimicrobial wash and Betadine will have an equal reduction in the incidence of C. acnes as Hydrogen Peroxide.",[29,202],"Positive C. Acnes Culture",[29,204,205,206],"Antimicrobial","Post-incision wash","C. Acnes","2025-05-30",{"date":209,"type":35},"2025-06-04",{"date":211,"type":35},"2025-05-05",{"date":213,"type":21},"2027-09",{"name":215,"class":42},"Henry Ford Health System",{"id":217,"slug":218,"hasResults":11,"nctId":219,"briefTitle":220,"officialTitle":221,"acronym":222,"eligibilityCriteria":223,"healthyVolunteers":11,"sex":16,"minAge":124,"maxAge":4,"enrollmentInfo":224,"targetDuration":4,"studyType":22,"phases":226,"briefSummary":227,"conditions":228,"keywords":232,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":233,"lastUpdatePostDateStruct":234,"startDateStruct":236,"completionDateStruct":238,"leadSponsor":240,"locationsCount":43},"100492967","shoulder-prosthesis-telerehab-care-trial-100492967","NCT05699031","Shoulder Prosthesis Telerehab Care Trial","The PROTECT-study: Home-based Telerehabilitation in the Post-operative Care After Shoulder Arthroplasty Compared to Usual Care: a Randomized Control Trial","PROTECT","Inclusion Criteria:\n\n* 60 years and older\n* primary total shoulder arthroplasty (anatomical and reverse)\n* osteoarthritis, cuff tear arthropathy, pseudoparalysis\n* return home after discharge from hospital\n* no brace after surgery\n* sufficient verbal and written comprehension\n* hospitalization insurance\n\nExclusion Criteria:\n\n* revision arthroplasty\n* arthroplasty for fracture or tumor\n* neurological disease (parkinson, stroke, ...)\n* no access to smartphone, tablet or internet connectivity",{"count":225,"type":21},120,[24],"The goal of this clinical trial is to compare the rehabilitation by use of a smartphone-app with the usual care of physical therapy in patients, 60 years and older, who underwent a primary shoulder arthroplasty.\n\nThe main questions it aims to answer are:\n\n* is the outcome of rehabilitation with the app as good as the usual care?\n* is the outcome for both types of shoulder arthroplasty similar?\n* what is the usability of the app?.\n\nParticipants will\n\n* have treatment according to the group they are allocated to\n* fill in questionnaires at specific moments during the rehabilitation stage (0 - 3 months ) and at 1 year post-surgery",[229,230,231],"SHOULDER ARTHROPLASTY","REHABILITATION","TELEREHABILITATION",[229,230,231],"2024-04-11",{"date":235,"type":35},"2024-04-12",{"date":237,"type":35},"2023-03-01",{"date":239,"type":21},"2026-09-30",{"name":241,"class":42},"University Hospital, Ghent"]