[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100603093":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":36,"locations":46,"responsibleParty":61,"collaborators":65,"id":69,"slug":26,"hasResults":70,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":74,"eligibilityCriteria":75,"healthyVolunteers":70,"sex":76,"minAge":77,"maxAge":26,"enrollmentInfo":78,"targetDuration":26,"studyType":81,"phases":82,"briefSummary":84,"conditions":85,"keywords":88,"overallStatus":91,"whyStopped":26,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":101},{"fullName":5,"class":6},"University Hospital, Basel, Switzerland","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Acupuncture:","EXPERIMENTAL","8 sessions of acupuncture treatment, once a week",[13],"Procedure: Acupuncture",{"label":15,"type":16,"description":17,"interventionNames":18},"Wait-listed control group","PLACEBO_COMPARATOR","Supportive care according to local standards will be given which may also include face-to-face psychosocial support or the participation of support groups. 8 weeks after the assessment T1 and upon completion of assessment T2, participants will receive access to 8 sessions of weekly acupuncture treatment.",[19],"Other: Standard supportive care",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"PROCEDURE","Acupuncture","8 sessions of acupuncture treatment (body and auricular acupuncture) will be given once a week after randomization.",[9],null,{"type":6,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Standard supportive care","Supportive care according to local standards will be given which may also include face-to-face psychosocial support or the participation of support groups",[15],[32],{"name":33,"affiliation":34,"role":35},"Viola Heinzelmann-Schwarz, Prof.MD","University Hospital of Basel","STUDY_CHAIR",[37,42],{"name":38,"role":39,"phone":40,"phoneExt":26,"email":41},"Isabell Xiang Ge, MD","CONTACT","+41 61 265 85885","isabellxiang.ge@usb.ch",{"name":43,"role":39,"phone":44,"phoneExt":26,"email":45},"Christian Kurzeder, Prof.MD","+41 61 32 87990","christian.kurzeder@usb.ch",[47],{"facility":48,"status":26,"city":49,"state":26,"zip":50,"country":51,"countryCode":52,"cosmosGeoPoint":53,"geoPoint":58,"contacts":59},"University Hospital Basel","Basel","4031","Switzerland","CH",{"type":54,"coordinates":55},"Point",[56,57],7.57327,47.55839,{"lat":57,"lon":56},[60],{"name":38,"role":39,"phone":40,"phoneExt":26,"email":41},{"type":62,"investigatorFullName":63,"investigatorTitle":64,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"SPONSOR_INVESTIGATOR","Isabell Xiang Ge","Dr. med.",[66],{"name":67,"class":68},"Swiss GO Trial Group","NETWORK","100603093",false,"NCT07132034","Stress Reduction Through Acupuncture","Study Protocol: Stress Reduction in Breast Cancer Patients During Transition Into Survivorship Using Acupuncture - a Randomized Wait-list-controlled Intervention Study","STREAK","Inclusion criteria:\n\n* Patients with localized breast cancer having completed primary therapy (operation +\u002F- chemotherapy +\u002F- radiotherapy) in the last 6 months - Distress Thermometer ≥ 5 - Age ≥ 18 years - Signed informed consent for participation of the trial\n* Prior cancer is allowed\n* Prior treatment - including chemotherapy - for a prior malignant tumor (including breast cancer) is allowed\n* Concomitant participation in an experimental therapeutic drug trial is allowed\n* Ongoing or planned Anti-her2\u002Fneu, immune checkpoint inhibitor, antihormonal and CDK4\u002F6 inhibitor therapy or other adjuvant treatment scheduled for \\> 3 months during study period is allowed\n* Use of other complementary methods (including mistletoe) is allowed.\n\nExclusion criteria:\n\n* Patients with language or cognitive deficits (including impaired consciousness) that are incompatible with the participation in the study\n* Severe physical or psychiatric comorbidity that prevents a patient from participating in the study\n* Patients incapable of giving consent\n* Pregnancy","FEMALE","18 Years",{"count":79,"type":80},112,"ESTIMATED","INTERVENTIONAL",[83],"NA","This randomized controlled trial evaluates whether eight weeks of weekly acupuncture can reduce psychological distress in breast cancer patients who have recently completed primary therapy compared to standard-of-care wait-list control.",[23,86,87],"Breast Cancer","Survivorship",[89,23,86,87,90],"Integrative Oncology","Distress","NOT_YET_RECRUITING","2026-05-19",{"date":94,"type":95},"2026-05-22","ACTUAL",{"date":97,"type":80},"2026-06",{"date":99,"type":80},"2028-09",{"name":63,"class":6},1]