[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT07461493":3,"trial-entities:NCT07461493":100,"trial-summary:NCT07461493":104},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":6,"overall_status":7,"completion_date":8,"status_verified_date":9,"last_update_date":10,"start_date":11,"sponsor_name":12,"lead_sponsor_class":13,"has_dmc":14,"brief_summary":15,"detailed_description":16,"conditions":17,"keywords":20,"study_type":35,"primary_purpose":16,"phases":36,"enrollment_info":37,"interventions":40,"primary_outcomes":41,"secondary_outcomes":46,"sex":50,"minimum_age":51,"maximum_age":16,"healthy_volunteers":14,"eligibility_criteria":52,"std_ages":56,"locations":59,"central_contacts":96,"overall_officials":97,"references":98,"see_also_links":99},"NCT07461493","CSSI-ED-25","The Cancer Stage Shifting Initiative: Registry and Biorepository to Research and Address Health Disparities in Cancer Care","RECRUITING","2039-03","2026-04","2026-04-08","2025-03-11","National Minority Quality Forum","OTHER",true,"The goal of this observational study is to establish a patient registry and a biorepository (sample collection and storage) to investigate health disparities, access, and barriers to cancer screening and early detection technologies. The registry and biorepository will serve as a resource to support Cancer Early Detection (CED) screenings and future research focused on communities at increased risk for cancer.\n\nThe study seeks to address:\n\n•Barriers and disparities in cancer prevention, screening, and treatment, particularly in historically underrepresented populations.\n\nParticipants will:\n\n* Attend a minimum of five clinic visits over a five-year period for scheduled annual assessments while actively enrolled in the study.\n* Complete questionnaires at each visit that collect information on their medical history, cancer history, and family cancer history.\n* Allow relevant health information from their electronic health records (EHR) to be collected and reviewed.\n* Provide blood, saliva, and stool samples for research purposes.\n* Enter a long-term follow-up period for an additional five years.",null,[18,19],"Cancer","Cancer Comorbidities",[21,18,22,23,24,25,26,27,12,28,29,30,31,32,33,34],"Early Detection","Registry","Biorepository","Cancer cluster","CSSI","Cancer Stage Shifting Initiative","NMQF","Health Disparities","Oncology","Cancer Screening","Tumor","superfund","environmental risks","SDOH","OBSERVATIONAL",[],{"count":38,"type":39},100000,"ESTIMATED",[],[42],{"measure":43,"description":44,"timeFrame":45},"Establish a patient registry","The primary objective of this study is to establish a patient registry that collects and characterizes health data from marginalized and underserved communities.","From enrollment to the end of follow up at 10 years.",[47],{"measure":48,"description":49,"timeFrame":45},"Establish a biorepository","The secondary objective of this study is to establish a unique biorepository that collects and characterizes biological samples from marginalized and underserved communities. This biorepository will focus on cancer incidence, stage, type, and geography and enable exploratory research towards the development of novel early detection technologies.","ALL","35 Years",{"inclusion":53,"exclusion":54,"raw_text":55},[],[],"Registry\n\nInclusion Criteria:\n\n1. Adults 35 years and older.\n2. Participant provides written informed consent prior to initiation of any study procedures.\n3. Participant understands the purpose and procedures of the study.\n4. Participant agrees that demographic data, medical history, and social determinants of health on the enrollment questionnaires can be used for research purposes.\n5. Participant agrees to the release and review of their electronic medical record.\n6. Participant agrees to be followed for the duration outlined in this protocol.\n\nBiorepository\n\n1. Participant is able, in the investigator's professional opinion, to provide up to 100 mLs of whole blood at the Screening Visit and at the Interim Visits.\n2. Participant is a healthy, nonpregnant adult.\n3. Participant weighs at least 110 pounds.\n4. Participant has negative viral test results.\n\nExclusion Criteria:\n\nRegistry\n\n1. Any medical or mental condition that would interfere with the subjects' ability to willingly give written informed consent.\n2. Participants who are unable to understand the study protocol or unable to give informed consent.\n3. Participants under the age of 35 at the time of enrollment.\n\nBiorepository\n\n1. Women of childbearing age that think they may be pregnant or are planning to get pregnant within the study timeframe.\n2. Participants who weigh under 110 pounds.\n3. Participants who, in the opinion of the investigator, are unable to provide biospecimen samples.",[57,58],"ADULT","OLDER_ADULT",[60,80],{"facility":61,"status":7,"city":62,"state":63,"zip":64,"country":65,"contacts":66,"geoPoint":77},"Life in 3D Health Services","Flint","Michigan","48507","United States",[67,72,75],{"name":68,"role":69,"phone":70,"email":71},"Denika Dalton, DNP-C","CONTACT","810-780-4189","Denika@lifeinddd.com",{"name":73,"role":74},"Rockefeller Oteng, MD","PRINCIPAL_INVESTIGATOR",{"name":68,"role":76},"SUB_INVESTIGATOR",{"lat":78,"lon":79},43.01253,-83.68746,{"facility":81,"status":7,"city":82,"state":83,"zip":84,"country":65,"contacts":85,"geoPoint":93},"Grace Clinic","Houston","Texas","77026",[86,90,92],{"name":87,"role":69,"phone":88,"email":89},"Sheila Young, FNP-BC","713-993-6000","appt@graceclinichouston.com",{"name":91,"role":74},"Chi Si Choi, MD",{"name":87,"role":76},{"lat":94,"lon":95},29.76328,-95.36327,[],[],[],[],{"nct_id":4,"conditions":101,"biomarkers":103},[102],"Malignant Neoplasm",[],{"nct_id":4,"found":14,"summary":105,"prompt_version":115},{"design":106,"status":107,"heading":108,"summary":109,"follow_up":110,"word_count":111,"commitments":112,"compensation":113,"drugs_mentioned":114},"This is an observational study that aims to enroll 100,000 participants. It is not testing any specific intervention.","completed","The Cancer Stage Shifting Initiative: Registry and Biorepository","This is an observational study, meaning it doesn't test a specific treatment but rather collects information. Its main goal is to create a large registry (a collection of health information) and a biorepository (a collection of biological samples) to better understand cancer. Researchers want to investigate why some groups of people face more challenges in getting cancer screenings and early detection. This study is open to adults aged 35 and older who are willing to share their health information and demographic data. The study aims to establish this registry and biorepository over 10 years to support future research, especially for communities at higher risk for cancer.","Participants will be followed from enrollment to the end of follow-up at 10 years.",106,"You would attend a minimum of five clinic visits over a five-year period for annual assessments.","Not stated in the trial record.",[],"v2"]