[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100632409":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":29,"centralContacts":33,"locations":38,"responsibleParty":54,"collaborators":57,"id":61,"slug":25,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":9,"eligibilityCriteria":66,"healthyVolunteers":62,"sex":67,"minAge":68,"maxAge":25,"enrollmentInfo":69,"targetDuration":25,"studyType":72,"phases":73,"briefSummary":75,"conditions":76,"keywords":78,"overallStatus":40,"whyStopped":25,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":92},{"fullName":5,"class":6},"Massachusetts General Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"RESTORE","EXPERIMENTAL","RESTORE is delivered as five weekly one-hour virtual (teleconference) sessions in small groups with a trained nurse and two 15-minute check-in phone calls later in the study. Participants will complete questionnaires at enrollment, 12-weeks, and 24-weeks post-enrollment.",[13],"Behavioral: RESTORE",{"label":15,"type":16,"description":17,"interventionNames":18},"Enhanced Usual Care","ACTIVE_COMPARATOR","Participants will receive educational information on breast cancer survivorship care in addition to usual care. Participants will complete questionnaires at enrollment, 12-weeks and 24-weeks post-enrollment. Participants will be offered one optional RESTORE intervention session after completing the 24-week questionnaire.",[19],"Behavioral: Enhanced Usual Care",[21,26],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"BEHAVIORAL","RESTORE is a nurse-led, small group-based, virtual (teleconference) cognitive-behavioral therapy-based intervention. The intervention incorporates psychoeducation, problem-solving, cognitive restructuring, relaxation training, symptom management skills training, coping effectiveness training, and mindfulness techniques.",[9],null,{"type":22,"name":15,"description":27,"armGroupLabels":28,"otherNames":25},"Participants will receive educational information on breast cancer survivorship care in addition to usual care.",[15],[30],{"name":31,"affiliation":5,"role":32},"Kathryn E Post, PhD, RN, ANP-BC","PRINCIPAL_INVESTIGATOR",[34],{"name":31,"role":35,"phone":36,"phoneExt":25,"email":37},"CONTACT","617-726-6500","kepost@mgh.harvard.edu",[39],{"facility":5,"status":40,"city":41,"state":42,"zip":43,"country":44,"cosmosGeoPoint":45,"geoPoint":50,"contacts":51},"RECRUITING","Boston","Massachusetts","02144","United States",{"type":46,"coordinates":47},"Point",[48,49],-71.05977,42.35843,{"lat":49,"lon":48},[52,53],{"name":31,"role":35,"phone":36,"phoneExt":25,"email":37},{"name":31,"role":32,"phone":25,"phoneExt":25,"email":25},{"type":32,"investigatorFullName":55,"investigatorTitle":56,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"Kathryn E. Post, PhD, RN, ANP-BC","Principal Investigator",[58],{"name":59,"class":60},"National Cancer Institute (NCI)","NIH","100632409",false,"NCT07513311","A Nurse-Led, Coping and Supportive Intervention for Patients With Triple-Negative Breast Cancer","Pilot Feasibility Trial of a Nurse-Led, Coping and Supportive Intervention (RESTORE) for Patients With Triple-Negative Breast Cancer","Inclusion Criteria:\n\n* Diagnosis of stage 1-3 triple-negative breast cancer\n* Age ≥ to 18 years\n* Between one and 12 months post curative therapy\n* Reporting distress at least 4\u002F10 on a one-item screener\n* Ability to read and respond in English or Spanish\n\nExclusion Criteria:\n\n* Patients with stage 4 cancer\n* Patients with impaired cognition or serious mental illness that would preclude participation in study procedures","ALL","18 Years",{"count":70,"type":71},75,"ESTIMATED","INTERVENTIONAL",[74],"NA","The purpose of this study is to explore the feasibility and acceptability of a nurse-led, coping, and supportive care intervention for patients with triple-negative breast cancer. The intervention aims to improve psychosocial outcomes in patients with triple-negative breast cancer (e.g., quality of life (QOL), anxiety, fear of cancer recurrence (FCR)).",[77],"Triple Negative Breast Cancer (TNBC)",[79,80,81,82],"triple negative breast cancer","coping","supportive care","nurse-led intervention","2026-06-11",{"date":85,"type":86},"2026-06-15","ACTUAL",{"date":88,"type":71},"2026-06",{"date":90,"type":71},"2028-07-31",{"name":5,"class":6},1]