[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100641275":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":29,"centralContacts":33,"locations":38,"responsibleParty":55,"collaborators":24,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":61,"acronym":24,"eligibilityCriteria":62,"healthyVolunteers":59,"sex":63,"minAge":64,"maxAge":24,"enrollmentInfo":65,"targetDuration":24,"studyType":68,"phases":69,"briefSummary":71,"conditions":72,"keywords":24,"overallStatus":77,"whyStopped":24,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":87},{"fullName":5,"class":6},"M.D. Anderson Cancer Center","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"COPE Intervention","EXPERIMENTAL","There are seven sessions within the COPE intervention. Sessions will be facilitated by a research team member weekly over the course of seven weeks and each session will take approximately 45 minutes.",[13],"Other: Intervention sessions",{"label":15,"type":6,"description":16,"interventionNames":17},"Control Group","Usual care will consist of standard care provided by the participant's healthcare team, including any recommendations regarding coping with stress, anxiety, depressive symptoms, resilience, and quality of life related to their breast cancer diagnosis and treatment.",[18],"Other: Standard of Care (SOC)",[20,25],{"type":6,"name":21,"description":22,"armGroupLabels":23,"otherNames":24},"Standard of Care (SOC)","Given by Questionnaires",[15],null,{"type":6,"name":26,"description":27,"armGroupLabels":28,"otherNames":24},"Intervention sessions","7 week sessions",[9],[30],{"name":31,"affiliation":5,"role":32},"Eileen D Hacker, MD","PRINCIPAL_INVESTIGATOR",[34],{"name":31,"role":35,"phone":36,"phoneExt":24,"email":37},"CONTACT","713-563-4004","ehacker@mdanderson.org",[39],{"facility":40,"status":24,"city":41,"state":42,"zip":43,"country":44,"countryCode":45,"cosmosGeoPoint":46,"geoPoint":51,"contacts":52},"MD Anderson Cancer Center","Houston","Texas","77030","United States","US",{"type":47,"coordinates":48},"Point",[49,50],-95.36327,29.76328,{"lat":50,"lon":49},[53,54],{"name":31,"role":35,"phone":36,"phoneExt":24,"email":37},{"name":31,"role":32,"phone":24,"phoneExt":24,"email":24},{"type":56,"investigatorFullName":24,"investigatorTitle":24,"investigatorAffiliation":24,"oldNameTitle":24,"oldOrganization":24},"SPONSOR","100641275","creating-opportunities-for-personal-empowerment-cope-in-women-with-breast-cancer-during-first-line-therapy-a-pilot-randomized-controlled-trial-100641275",false,"NCT07610499","Creating Opportunities For Personal Empowerment (COPE) In Women With Breast Cancer During First-Line Therapy: A Pilot Randomized Controlled Trial","Eligibility Criteria\n\n* Female\n* Age 18 years and older\n* Diagnosed with stage I-III breast cancer\n* Receiving first line treatment for breast cancer\n* Receiving treatment at MD Anderson\n* Able to read, speak, and consent in English\n* Able to understand and be willing to sign a written informed consent document\n* Able to complete the study questionnaires and intervention sessions\n\nExclusion Criteria\n\n* Diagnosed with multiple tumor types\n* Diagnosed with stage IV breast cancer\n* Unable to provide consent, such as cognitively impaired individuals\n* Has a preexisting psychiatric diagnosis (e.g., bipolar depression)","FEMALE","18 Years",{"count":66,"type":67},40,"ESTIMATED","INTERVENTIONAL",[70],"NA","To learn if the Creating Opportunities for Personal Empowerment (COPE) intervention is feasible, acceptable, and helpful (compared to usual care) in women with breast cancer who are receiving first line treatment.",[73,74,75,76],"COPE","Breast Cancer","First Line Therapy","Randomized Controlled Trial (RCT)","NOT_YET_RECRUITING","2026-05-20",{"date":80,"type":81},"2026-05-28","ACTUAL",{"date":83,"type":67},"2026-10-30",{"date":85,"type":67},"2029-05-01",{"name":5,"class":6},1]