[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT05654246":3,"trial-entities:NCT05654246":81,"trial-summary:NCT05654246":85},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":7,"overall_status":8,"completion_date":9,"status_verified_date":10,"last_update_date":11,"start_date":12,"sponsor_name":13,"lead_sponsor_class":14,"has_dmc":15,"brief_summary":16,"detailed_description":17,"conditions":18,"keywords":20,"study_type":21,"primary_purpose":22,"phases":23,"enrollment_info":24,"interventions":27,"primary_outcomes":28,"secondary_outcomes":39,"sex":40,"minimum_age":41,"maximum_age":22,"healthy_volunteers":42,"eligibility_criteria":43,"std_ages":55,"locations":58,"central_contacts":74,"overall_officials":76,"references":79,"see_also_links":80},"NCT05654246","SGK-SFC-001","Susan G. Komen's ShareForCures","ShareForCures: Susan G. Komen's People-powered, Data-driven Breast Cancer Research Registry","RECRUITING","2032-11","2026-03","2026-03-06","2022-11-17","Susan G. Komen Breast Cancer Foundation","OTHER",true,"ShareForCures (SFC) is a community-based participatory research registry, and its prime objective is to engage participants representative of the United States breast cancer patient population -including minoritized and historically marginalized people, persons, or communities-to ensure the data researchers use to study breast cancer is as diverse as the people touched by this disease. In doing so, researchers will have a better understanding of breast cancer, and everyone can potentially benefit from scientific advances and improvements in care.","ShareForCures (SFC) will be a people-powered, data-driven breast cancer registry that will provide a way for individuals from diverse backgrounds to participate in research and enable participants' data to be used for breast cancer research. The overarching goal of SFC is to create a robust research resource comprised of clinical, biological, socio-behavioral, and other data from up to 200,000 people with breast cancer-including minoritized and historically marginalized people, persons, or communities-to ensure the data, researchers use to study breast cancer, is as diverse as the people touched by this disease. In doing so, researchers will have a better understanding of breast cancer and everyone can potentially benefit from scientific advances and improvements in care.",[19],"Breast Cancer",[],"OBSERVATIONAL",null,[],{"count":25,"type":26},200000,"ESTIMATED",[],[29,33,36],{"measure":30,"description":31,"timeFrame":32},"Engage participants representative of the United States breast cancer patient population in ShareForCures.","Enroll and engage up to 200,000 people, who have been diagnosed with breast cancer, reflecting the diversity of breast cancer survivors within the United States, to participate in the registry as our partners in research.","10 years",{"measure":34,"description":35,"timeFrame":32},"Integrate participant data into ShareForCures.","Collect and curate a rich scope of participant data from a variety of sources (including participant-provided information, clinical records, and linkage to other existing datasets) and biospecimens to create a comprehensive, longitudinal database.",{"measure":37,"description":38,"timeFrame":32},"Facilitate scientific research using ShareForCures data.","Make deidentified data available to researchers for scientific discoveries, including research that may lead to new knowledge about breast cancer and advances in patient care and outcomes.",[],"ALL","18 Years",false,{"inclusion":44,"exclusion":49,"raw_text":54},[45,46,47,48],"Individuals must be at least 18 years old. (Individuals in Alabama and Nebraska must be over 19 and individuals in Mississippi and Pennsylvania must be over 21 to participate).","Individuals must have been diagnosed with cancer originating (or is suspected to originate) from the breast.","Individuals must be currently residing in the United States or a territory of the United States.","Individuals must be able to read and understand English.",[50,51,52,53],"Individuals under the age of 18 years. (Individuals in Alabama and Nebraska under 19 and individuals in Mississippi and Pennsylvania under 21 are not eligible to participate).","Individuals without a diagnosis of breast cancer.","Individuals who are not residing in the United States or a territory of the United States.","Individuals unable to read and understand English.","Inclusion Criteria:\n\n* Individuals must be at least 18 years old. (Individuals in Alabama and Nebraska must be over 19 and individuals in Mississippi and Pennsylvania must be over 21 to participate).\n* Individuals must have been diagnosed with cancer originating (or is suspected to originate) from the breast.\n* Individuals must be currently residing in the United States or a territory of the United States.\n* Individuals must be able to read and understand English.\n\nExclusion Criteria:\n\n* Individuals under the age of 18 years. (Individuals in Alabama and Nebraska under 19 and individuals in Mississippi and Pennsylvania under 21 are not eligible to participate).\n* Individuals without a diagnosis of breast cancer.\n* Individuals who are not residing in the United States or a territory of the United States.\n* Individuals unable to read and understand English.",[56,57],"ADULT","OLDER_ADULT",[59],{"facility":60,"status":8,"city":61,"state":62,"zip":63,"country":64,"contacts":65,"geoPoint":71},"Susan G. Komen","Dallas","Texas","75380","United States",[66],{"name":67,"role":68,"phone":69,"email":70},"Jerome Jourquin, Ph.D., M.S.","CONTACT","1-877-465-6636","JJourquin@komen.org",{"lat":72,"lon":73},32.78306,-96.80667,[75],{"name":67,"role":68,"phone":69,"email":70},[77],{"name":67,"affiliation":60,"role":78},"PRINCIPAL_INVESTIGATOR",[],[],{"nct_id":4,"conditions":82,"biomarkers":84},[83],"Breast Carcinoma",[],{"nct_id":4,"found":15,"summary":86,"prompt_version":96},{"design":87,"status":88,"heading":89,"summary":90,"follow_up":91,"word_count":92,"commitments":93,"compensation":94,"drugs_mentioned":95},"This is an observational study aiming to enroll up to 200,000 participants. It is a community-based participatory research registry.","completed","Susan G. Komen's ShareForCures for Breast Cancer Research","This study, called ShareForCures, is creating a large collection of health information from people with breast cancer across the United States. The goal is to gather diverse data, including from groups often underrepresented in research, to help scientists better understand breast cancer. By making this information available, researchers hope to improve breast cancer care for everyone. You can join if you are at least 18 years old (or 19 in Alabama and Nebraska, 21 in Mississippi and Pennsylvania) and have been diagnosed with breast cancer. The study aims to engage participants, integrate their data, and facilitate scientific research over 10 years.","Participant data will be integrated and used for scientific research for up to 10 years.",101,"Not specified in the trial record.","Not stated in the trial record.",[],"v2"]