[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100582835":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":11,"centralContacts":29,"locations":39,"responsibleParty":57,"collaborators":11,"id":61,"slug":62,"hasResults":63,"nctId":64,"briefTitle":65,"officialTitle":65,"acronym":66,"eligibilityCriteria":67,"healthyVolunteers":63,"sex":68,"minAge":69,"maxAge":11,"enrollmentInfo":70,"targetDuration":11,"studyType":73,"phases":74,"briefSummary":76,"conditions":77,"keywords":79,"overallStatus":82,"whyStopped":11,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":92},{"fullName":5,"class":6},"University of Witten\u002FHerdecke","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Prehabilitation-Group","ACTIVE_COMPARATOR",null,[13],"Procedure: Prehabilitation",{"label":15,"type":16,"description":11,"interventionNames":17},"Control-Group","PLACEBO_COMPARATOR",[18],"Procedure: Control",[20,25],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":11},"PROCEDURE","Prehabilitation","The waiting time until the operation is about 6 weeks. The intervention is carried out during this time:\n\nThe intervention group receives a brochure with an evidence-based exercise program for the shoulder and shoulder girdle. The brochure contains pages in which the patient documents how the exercises are carried out. The exercise program is supplemented by information in the form of a video\u002FPower Point presentation on: Anatomy\u002Ffunction, pain management, hospitalization and subsequent rehabilitation.\n\nAfter 2 and after 4 weeks, the physiotherapist who has explained the exercise program will contact you by telephone\u002Fzoom.",[9],{"type":21,"name":26,"description":27,"armGroupLabels":28,"otherNames":11},"Control","The control group receives a leaflet with general information for the period up to the operation (e.g. buy water-resistant plasters, arrange post-op physiotherapy appointments).",[15],[30,35],{"name":31,"role":32,"phone":33,"phoneExt":11,"email":34},"Arasch Wafaisade, Prof. Dr. med.","CONTACT","+49-221-8907-18600","WafaisadeA@kliniken-koeln.de",{"name":36,"role":32,"phone":37,"phoneExt":11,"email":38},"Ute Westphal","+49-221-8907-2421","Westphalu@kliniken-koeln.de",[40],{"facility":41,"status":11,"city":42,"state":11,"zip":43,"country":44,"countryCode":45,"cosmosGeoPoint":46,"geoPoint":51,"contacts":52},"Kliniken der Stadt Köln gGmbH","Cologne","51067","Germany","DE",{"type":47,"coordinates":48},"Point",[49,50],6.95,50.93333,{"lat":50,"lon":49},[53,55],{"name":31,"role":32,"phone":54,"phoneExt":11,"email":34},"+49221 890718600",{"name":36,"role":32,"phone":56,"phoneExt":11,"email":38},"+49221 89072429",{"type":58,"investigatorFullName":59,"investigatorTitle":60,"investigatorAffiliation":5,"oldNameTitle":11,"oldOrganization":11},"SPONSOR_INVESTIGATOR","Prof. Arasch Wafaisade","Prof. Dr. med.","100582835","early-recovery-after-surgery-erasprehabilitation---randomized-controlled-trial-on-the-implementation-of-erasprehabilitation-in-elective-reconstructive-shoulder-surgery-100582835",false,"NCT06868472","Early Recovery After Surgery (ERAS)\u002FPrehabilitation - Randomized Controlled Trial on the Implementation of ERAS\u002Fprehabilitation in Elective Reconstructive Shoulder Surgery","Prehab","Inclusion Criteria:\n\n* Patients with a traumatic or degenerative rupture of the rotator cuff with whom surgical treatment has been discussed in the shoulder clinic.\n\nExclusion Criteria:\n\n* Pre-existing fracture of the upper arm or shoulder girdle, rheumatic arthritis\u002Ffibromyalgia, additional findings in the shoulder joint (instability, frozen shoulder), neurological disease, cognitive or speech impairment","ALL","18 Years",{"count":71,"type":72},84,"ESTIMATED","INTERVENTIONAL",[75],"NA","The aim of this randomized controlled trial is to investigate whether the intervention can improve the clinical outcome and patient satisfaction in elective reconstructive shoulder surgeries. The study participants are adults with a diagnosed rotator cuff tear for which surgical treatment is planned. This main question is to be answered by the study:\n\n• Does prehabilitation before elective shoulder surgeries lead to an improvement in postoperative outcomes and patient satisfaction compared to the control group?\n\nThe control group receives standard information about the hospital stay, while the intervention group undergoes the prehabilitation program in the approximately 6 weeks prior to surgery. This program includes:\n\n* Information on the condition and pain management\n* Recommendations for behavior modification\n* A home exercise program Primary endpoint is the Western Ontario Rotator Cuff Index (WORC). The assessments are conducted at four time points: at study enrollment, immediately before surgery, and at 6, 12, and 24 months after surgery.",[78],"Rotator Cuff",[80,81],"Preoperative Exercise","Enhanced Recovery After Surgery","NOT_YET_RECRUITING","2025-03-06",{"date":85,"type":86},"2025-03-11","ACTUAL",{"date":88,"type":72},"2025-03-18",{"date":90,"type":72},"2029-02",{"name":59,"class":6},1]