[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100574585":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":7,"centralContacts":12,"locations":22,"responsibleParty":47,"collaborators":7,"id":49,"slug":50,"hasResults":51,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":51,"sex":57,"minAge":58,"maxAge":7,"enrollmentInfo":59,"targetDuration":7,"studyType":62,"phases":7,"briefSummary":63,"conditions":64,"keywords":67,"overallStatus":25,"whyStopped":7,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":81},{"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,"countryCode":29,"cosmosGeoPoint":30,"geoPoint":35,"contacts":36},"Hôpitaux Civils de Colmar","RECRUITING","Colmar","68024","France","FR",{"type":31,"coordinates":32},"Point",[33,34],7.35584,48.08078,{"lat":34,"lon":33},[37,39,42,45],{"name":38,"role":15,"phone":16,"phoneExt":7,"email":17},"Massimo Lodi, MD",{"name":40,"role":41,"phone":7,"phoneExt":7,"email":7},"Massimo Lodi","PRINCIPAL_INVESTIGATOR",{"name":43,"role":44,"phone":7,"phoneExt":7,"email":7},"Delphine Weitbruch","SUB_INVESTIGATOR",{"name":46,"role":44,"phone":7,"phoneExt":7,"email":7},"Sylvia Mazellier",{"type":48,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100574585","quality-of-life-after-breast-cancer-surgery-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":60,"type":61},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.",[65,66],"Breast Cancer Surgery","Quality of Life",[68,69,70,71],"breast cancer","oncoplastic surgery","quality of life","quality of recovery","2025-09-05",{"date":74,"type":75},"2025-09-08","ACTUAL",{"date":77,"type":75},"2025-09-02",{"date":79,"type":61},"2035-09-01",{"name":5,"class":6},1]