[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100366280":3},{"organization":4,"armGroups":7,"interventions":13,"overallOfficials":16,"centralContacts":17,"locations":23,"responsibleParty":39,"collaborators":16,"id":41,"slug":42,"hasResults":43,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":16,"eligibilityCriteria":47,"healthyVolunteers":43,"sex":48,"minAge":49,"maxAge":16,"enrollmentInfo":50,"targetDuration":16,"studyType":53,"phases":54,"briefSummary":56,"conditions":57,"keywords":16,"overallStatus":25,"whyStopped":16,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":69},{"fullName":5,"class":6},"Hoag Memorial Hospital Presbyterian","OTHER",[8],{"label":9,"type":6,"description":10,"interventionNames":11},"Meditation","Two guided meditations will be provided to participants. They will be asked to meditate twice daily, once in the morning once before bed, for a total time of 12 minutes per day. Surgical treatment and postoperative care will be provided by surgeon preference and usual practice, including post-operative pain medications. For 12 weeks patients will maintain a daily meditation log, medication log and complete daily pain assessment questionnaire.",[12],"Other: Meditation",[14],{"type":6,"name":9,"description":10,"armGroupLabels":15,"otherNames":16},[9],null,[18],{"name":19,"role":20,"phone":21,"phoneExt":16,"email":22},"Melinda Epstein, PhD","CONTACT","949-764-5543","clinicalresearch@hoag.org",[24],{"facility":5,"status":25,"city":26,"state":27,"zip":28,"country":29,"countryCode":30,"cosmosGeoPoint":31,"geoPoint":36,"contacts":37},"RECRUITING","Newport Beach","California","92663","United States","US",{"type":32,"coordinates":33},"Point",[34,35],-117.92895,33.61891,{"lat":35,"lon":34},[38],{"name":19,"role":20,"phone":21,"phoneExt":16,"email":22},{"type":40,"investigatorFullName":16,"investigatorTitle":16,"investigatorAffiliation":16,"oldNameTitle":16,"oldOrganization":16},"SPONSOR","100366280","perioperative-mindfulness-proposal-100366280",false,"NCT04049214","Perioperative Mindfulness Proposal","Feasibility Study to Determine the Effect of Meditation on Perioperative Pain and Distress in Newly Diagnosed Breast Cancer Patients","Inclusion Criteria:\n\n* Females 18 years of age or older\n* Subject must be able to speak and read English\n* Newly diagnosed with primary breast cancer\n* Will receive primary surgical treatment for their breast cancer diagnosis.\n* Undergoing lumpectomy with or without autologous reconstruction with or without contralateral surgery for symmetry with or without IORT or simple mastectomy without reconstruction\n* Breast cancer or DCIS\n\nExclusion Criteria:\n\n* Recurrent breast cancer\n* Current or history of major psychiatric diagnosis.\n* Subjects who are receiving neo-adjuvant chemotherapy\n* Subjects undergoing modified radical mastectomy or reconstruction\n* Subjects regular meditation practice within the past 12 months (defined as greater than twice weekly practice)\n* Subjects unwilling or unable to complete study materials or comply with study visits\n* Subjects with no access to email or a mobile phone (required to access meditations)\n* Subjects undergoing surgery outside Hoag\n* Subjects who have narcotic dependence as defined by regular weekly narcotic use before cancer diagnosis.\n* Re-excision after lumpectomy (subjects who require re-excision after initial enrollment will be excluded from final analysis and dropped from the study).","FEMALE","18 Years",{"count":51,"type":52},24,"ESTIMATED","INTERVENTIONAL",[55],"NA","The purpose of this study is to determine if a regular meditation and breath work practice started before surgery and continued through post-surgical recovery can improve anxiety and pain related to breast cancer and its treatment.",[58,59],"Breast Cancer","DCIS","2024-10-09",{"date":62,"type":63},"2024-10-15","ACTUAL",{"date":65,"type":63},"2019-07-31",{"date":67,"type":52},"2025-07-31",{"name":5,"class":6},1]