[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100556053":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":24,"centralContacts":24,"locations":25,"responsibleParty":47,"collaborators":49,"id":53,"slug":54,"hasResults":55,"nctId":56,"briefTitle":57,"officialTitle":57,"acronym":58,"eligibilityCriteria":59,"healthyVolunteers":55,"sex":60,"minAge":61,"maxAge":24,"enrollmentInfo":62,"targetDuration":24,"studyType":65,"phases":66,"briefSummary":68,"conditions":69,"keywords":71,"overallStatus":76,"whyStopped":24,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},{"fullName":5,"class":6},"VieCuri Medical Centre","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Personalized rehabilitation program","EXPERIMENTAL","The intervention group receives an interactive app that is different from the control is different from the control group in that it provides interactive and personalized information and a personalized rehabilitation program. Both the timing and the amount and nature of the exercises are personalized.",[13],"Other: interactive mHealth application for patients undergoing RSA",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard care","ACTIVE_COMPARATOR","The control group will receive postoperative information and a rehabilitation program via the non-interactive application, which is current standard care",[13],[20],{"type":6,"name":21,"description":22,"armGroupLabels":23,"otherNames":24},"interactive mHealth application for patients undergoing RSA","Patients will receive interactive information via an mHealth application tailored to their needs and progress during the rehabilitation period after RSA.",[9,15],null,[26],{"facility":27,"status":24,"city":28,"state":29,"zip":30,"country":31,"countryCode":32,"cosmosGeoPoint":33,"geoPoint":38,"contacts":39},"VieCuri Medisch Centrum","Venlo","Limburg","5912BL","Netherlands","NL",{"type":34,"coordinates":35},"Point",[36,37],6.16806,51.37,{"lat":37,"lon":36},[40,44],{"name":41,"role":42,"phone":24,"phoneExt":24,"email":43},"Esther Janssen, PhD","CONTACT","estherjanssen@viecuri.nl",{"name":45,"role":42,"phone":24,"phoneExt":24,"email":46},"Janneke Crutsen, MSc","jcrutsen@viecuri.nl",{"type":48,"investigatorFullName":24,"investigatorTitle":24,"investigatorAffiliation":24,"oldNameTitle":24,"oldOrganization":24},"SPONSOR",[50],{"name":51,"class":52},"Anna ziekenhuis","UNKNOWN","100556053","optimizing-recovery-after-reverse-shoulder-arthroplasty-with-a-personalized-mobile-health-application-100556053",false,"NCT06520085","Optimizing Recovery After Reverse Shoulder Arthroplasty With a Personalized Mobile Health Application","TRAPP","Inclusion Criteria:\n\n* adults undergoing elective reverse shoulder arthroplasty\n\nExclusion Criteria:\n\n1\\) do not own or are not able to operate a smart device; 2) are scheduled for revision surgery; 3) have a fracture as primary diagnosis; 4) an additional muscle transfer needs to be performed; or 5) are unable to read and understand the Dutch language.","ALL","18 Years",{"count":63,"type":64},170,"ESTIMATED","INTERVENTIONAL",[67],"NA","Background: Mobile health (mHealth) - the use of medical applications in healthcare settings - include tools that can support self-management after surgery and thereby contribute to early postoperative recovery. Providing patients with timely and interactive information through mHealth is hypothesized to positively influence recovery after reverse shoulder arthroplasty (RSA).\n\nAim: The aim of this study is to determine the effectiveness of interactive and personalized information and rehabilitation protocol with a mobile application compared to generic information and generic rehabilitation protocol (standard care) on postoperative recovery in patients undergoing primary RSA.\n\nMethods and analysis: A multicentre randomised controlled trial will be conducted in two Dutch hospitals. In total 170 patients undergoing elective, primary RSA will be included. Participants will be randomly allocated to one of the two groups on a 1:1 ratio. The intervention group will receive interactive postoperative information on a daily basis. The control group will receive standard care. The primary outcome is defined as functional recovery measured using the Oxford Shoulder Score (OSS) at 6 weeks. Secondary outcomes are: pain, physical functioning, quality of life, length of stay, complications, treatment satisfaction and app use. The between group difference will be analysed using linear mixed-effects regression.",[70],"Shoulder Osteoarthritis",[72,73,74,75],"Reverse Shoulder Arthroplasty","mHealth","Perioperative Care","Rehabilitation","NOT_YET_RECRUITING","2024-07-22",{"date":79,"type":80},"2024-07-25","ACTUAL",{"date":82,"type":64},"2024-08-01",{"date":84,"type":64},"2026-12-31",{"name":5,"class":6},1]