[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100574585":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":7,"centralContacts":12,"locations":22,"responsibleParty":46,"collaborators":7,"id":48,"slug":7,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":49,"sex":55,"minAge":56,"maxAge":7,"enrollmentInfo":57,"targetDuration":7,"studyType":60,"phases":7,"briefSummary":61,"conditions":62,"keywords":65,"overallStatus":25,"whyStopped":7,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":79},{"fullName":5,"class":6},"Centre Hospitalier de Colmar","OTHER",null,[9],{"type":6,"name":10,"description":11,"armGroupLabels":7,"otherNames":7},"Questionnaire","The quality of life measured with different scales (BREAST-Q, EORTC QLQ C30 and BR42)",[13,18],{"name":14,"role":15,"phone":16,"phoneExt":7,"email":17},"Massimo LODI, MD","CONTACT","0033389124171","massimo.lodi@ch-colmar.fr",{"name":19,"role":15,"phone":20,"phoneExt":7,"email":21},"Magali EYRIEY","0033389124810","magali.eyriey@ch-colmar.fr",[23],{"facility":24,"status":25,"city":26,"state":7,"zip":27,"country":28,"cosmosGeoPoint":29,"geoPoint":34,"contacts":35},"Hôpitaux Civils de Colmar","RECRUITING","Colmar","68024","France",{"type":30,"coordinates":31},"Point",[32,33],7.35584,48.08078,{"lat":33,"lon":32},[36,38,41,44],{"name":37,"role":15,"phone":16,"phoneExt":7,"email":17},"Massimo Lodi, MD",{"name":39,"role":40,"phone":7,"phoneExt":7,"email":7},"Massimo Lodi","PRINCIPAL_INVESTIGATOR",{"name":42,"role":43,"phone":7,"phoneExt":7,"email":7},"Delphine Weitbruch","SUB_INVESTIGATOR",{"name":45,"role":43,"phone":7,"phoneExt":7,"email":7},"Sylvia Mazellier",{"type":47,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100574585",false,"NCT06761196","Quality of Life After Breast Cancer Surgery","Assessing Quality of Life After Breast Cancer Surgery: a Prospective Cohort Study","SOCOM-QoL","Inclusion Criteria:\n\n* Patient aged 18 or over\n* Patient with breast cancer of any stage (including in situ) or healthy individual at high personal risk.\n* Patient requiring breast surgery under general anesthesia, whether for therapeutic or prophylactic purposes.\n* Patient capable, in the opinion of the investigator, of complying with the requirements and restrictions of the study.\n* Patient with a computer, tablet or smartphone connected to the Internet.\n* Patient followed in the center on a regular basis according to standard recommendations.\n\nExclusion Criteria:\n\n* Patient requiring surgical intervention under local anesthesia only.\n* Patient requiring surgery for the installation or removal of an chemotherapy implantable port only.\n* Patients with a history of cancer other than breast cancer. Patients with a history of cancer more than three years old are eligible if they are treated and considered cured. Patients with a history of cervical carcinoma in situ or non-melanoma skin carcinoma are eligible.\n* Impossibility of being subject to regular monitoring for geographical, social or psychological reasons.\n* Patient under protective measure","ALL","18 Years",{"count":58,"type":59},1500,"ESTIMATED","OBSERVATIONAL","The goal of this observational study is to prospectively collect data on quality of life after oncoplastic breast surgery.\n\nParticipants will be followed-up and answer quality of life questionnaire for a duration of 5 years after surgery.",[63,64],"Breast Cancer Surgery","Quality of Life",[66,67,68,69],"breast cancer","oncoplastic surgery","quality of life","quality of recovery","2025-09-05",{"date":72,"type":73},"2025-09-08","ACTUAL",{"date":75,"type":73},"2025-09-02",{"date":77,"type":59},"2035-09-01",{"name":5,"class":6},1]