[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100625649":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":30,"locations":36,"responsibleParty":52,"collaborators":26,"id":55,"slug":26,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":26,"eligibilityCriteria":60,"healthyVolunteers":56,"sex":61,"minAge":62,"maxAge":63,"enrollmentInfo":64,"targetDuration":26,"studyType":67,"phases":68,"briefSummary":70,"conditions":71,"keywords":76,"overallStatus":82,"whyStopped":26,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":92},{"fullName":5,"class":6},"Bakirkoy Dr. Sadi Konuk Research and Training Hospital","OTHER_GOV",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Prehabilitation Group","EXPERIMENTAL","Participants will receive a structured home-based prehabilitation program delivered through written materials and instructional exercise videos (QR code access). The program includes:\n\nAerobic training (3\u002Fweek, 30-40 minutes, RPE 4-6) Upper extremity resistance exercises (3 days\u002Fweek, 3 sets of 10 repetitions) Mobility and stretching exercises\n\nAdherence will be monitored through weekly remote follow-up (telephone)",[13],"Other: Home-Based Prehabilitation Exercise Program",{"label":15,"type":16,"description":17,"interventionNames":18},"Usual Care","ACTIVE_COMPARATOR","Standard preoperative counseling without structured exercise prescription.",[19],"Other: Usual Care",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"OTHER","Home-Based Prehabilitation Exercise Program","Participants assigned to this arm will receive a structured, home-based prehabilitation program initiated at least three weeks prior to surgery. The intervention includes: (1) moderate-intensity aerobic exercise (3 sessions per week, 30 minutes per session, target intensity RPE 4-6\u002F10), (2) upper extremity resistance exercises using elastic bands (3 sessions per week, 3 sets of 10 repetitions per exercise), and (3) mobility and stretching exercises focused on shoulder function.\n\nThe program will be delivered through written materials and instructional exercise videos accessible via QR code. Participants will receive elastic resistance bands for training. Adherence and progression will be monitored weekly via remote follow-up (telephone or email contact). The intervention is non-pharmacological and designed to optimize upper extremity function prior to breast cancer surgery.",[9],null,{"type":22,"name":15,"description":28,"armGroupLabels":29,"otherNames":26},"Usual Preoperative Care",[15],[31],{"name":32,"role":33,"phone":34,"phoneExt":26,"email":35},"Demet Ferahman, MD","CONTACT","+905364702930","demetferahman@gmail.com",[37],{"facility":38,"status":26,"city":39,"state":39,"zip":40,"country":41,"cosmosGeoPoint":42,"geoPoint":47,"contacts":48},"Dr. Sadi Konuk Bakirkoy Training and Health Hospital","Istanbul","34140","Turkey (Türkiye)",{"type":43,"coordinates":44},"Point",[45,46],28.94966,41.01384,{"lat":46,"lon":45},[49],{"name":50,"role":33,"phone":51,"phoneExt":26,"email":35},"Demet Ferahman","05364702930",{"type":53,"investigatorFullName":50,"investigatorTitle":54,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","M.D.","100625649",false,"NCT07425379","Prehabilitation in Breast Cancer Surgery","Prehabilitation in Breast Cancer Surgery: A Prospective Randomized Controlled Trial Evaluating Shoulder Function, Pain, Quality of Life and Lymphedema Development","Inclusion Criteria:\n\nWomen aged 18-80\n\nStage I-III invasive breast cancer\n\nScheduled for surgery\n\n≥3 weeks before surgery\n\nNo neoadjuvant therapy\n\nExclusion Criteria:\n\nExercise contraindication\n\nActive shoulder pathology\n\nSevere cardiopulmonary disease\n\nPlanned neoadjuvant therapy","FEMALE","18 Years","80 Years",{"count":65,"type":66},54,"ESTIMATED","INTERVENTIONAL",[69],"NA","This prospective, randomized, assessor-blinded, parallel-group clinical trial evaluates the effectiveness of a home-based upper extremity-focused prehabilitation program in women undergoing breast cancer surgery. Participants will be randomized 1:1 to either prehabilitation or usual care. Primary outcomes include shoulder range of motion and upper extremity function (DASH score). Secondary outcomes include grip strength, pain, fatigue, disability, anxiety\u002Fdepression, and lymphedema incidence up to 2 years postoperatively.",[72,73,74,75],"Breast Cancer (Early Breast Cancer)","Postoperative Shoulder Dysfunction","Lymphedema Arm","Cancer Rehabilitation",[77,78,79,80,75,81],"Prehabilitation","Breast Cancer Surgery","Shoulder Range of Motion","Upper Extremity Function","Exercise Therapy","NOT_YET_RECRUITING","2026-02-23",{"date":85,"type":86},"2026-02-24","ACTUAL",{"date":88,"type":66},"2026-03-01",{"date":90,"type":66},"2028-12-01",{"name":5,"class":6},1]