[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Isabell Xiang Ge\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":45},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":5},"100603093","stress-reduction-through-acupuncture-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":20,"type":21},112,"ESTIMATED","INTERVENTIONAL",[24],"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.",[27,28,29],"Acupuncture","Breast Cancer","Survivorship",[31,27,28,29,32],"Integrative Oncology","Distress","NOT_YET_RECRUITING","2026-05-19",{"date":36,"type":37},"2026-05-22","ACTUAL",{"date":39,"type":21},"2026-06",{"date":41,"type":21},"2028-09",{"name":43,"class":44},"Isabell Xiang Ge","OTHER",""]