[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cancer-prevention\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cancer-prevention":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,48,75,104,127,149,177,208],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100605582","empowering-vietnamese-americans-100605582",false,"NCT07164391","Empowering Vietnamese Americans","Empowering Vietnamese Americans: A Culture-Centric Digital Storytelling Intervention to Boost HPV Vaccination","Inclusion Criteria: An individual is eligible if they:\n\n* Self-identify as a Vietnamese American or immigrant woman aged 18 years or older\n* Are the primary caregiver of at least one unvaccinated child aged 11-14 years\n* Can speak and read English or Vietnamese\n* Agree to receive text messages and\u002For emails related to project activities during the study period\n\nExclusion Criteria:\n\n* inability\u002Funwillingness to provide consent.",true,"ALL","18 Years",{"count":20,"type":21},60,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to learn whether short videos can help Vietnamese American mothers decide to vaccinate their children against HPV (human papillomavirus). The study will explore: (1) whether different interventions influence mothers' intentions and decisions regarding HPV vaccination for their children; (2) how mothers perceive and engage with the videos; and (3) how many children receive the HPV vaccine after their mothers watch the videos.\n\nParticipants will be randomly assigned to one of two groups: (a) watch four short digital stories about the HPV vaccine created by Vietnamese mothers; or (b) watch four short videos on general teen health topics such as mental health and social media use. Participants will complete brief surveys and their child's HPV vaccination status will be checked two months after the intervention.",[27,28],"HPV Vaccination","Cancer Prevention",[30,31,32,33,34],"HPV","cancer prevention","Vietnamese American","youth","digital storytelling","RECRUITING","2026-05-18",{"date":38,"type":39},"2026-05-20","ACTUAL",{"date":41,"type":39},"2025-10-01",{"date":43,"type":21},"2027-11-30",{"name":45,"class":46},"Michigan State University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":62,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":74},"100630667","nuestro-valor-increasing-healthier-food-access-for-rural-latino-communities-through-a-food-retail-intervention-100630667","NCT07490652","Nuestro Valor: Increasing Healthier Food Access for Rural Latino Communities Through a Food Retail Intervention","Inclusion criteria:\n\nIn order for an individual to participate in this study, the individual must meet all of the following criteria:\n\n* Identify as Latino or Hispanic\n* Be at least 18 years or older\n* Live in Benton, Franklin, or Yakima county for at least 6 months and plan to remain there for the next 12 months\n* Visit this store at least once per week\n* Be primary household shopper (conducting 50% of shopping duties)\n* Eat 4 or less servings of fruits and vegetables per week Only one participant per household will be recruited to ensure the independence of observations.\n\nExclusion criteria:\n\nSubjects who do not meet the inclusion criteria above will be excluded from the study. If any subject shows 3 or more visual signs of intoxication or impairment, they will be excluded from the study. The study team member will assess visual signs of intoxication during recruitment using the Oregon Liquor \\& Cannabis Commission 50 Signs of Visual Intoxication assessment. A link to these signs can be found here: https:\u002F\u002Fwww.oregon.gov\u002Folcc\u002Fdocs\u002Fpublications\u002F50\\_signs\\_visible\\_intoxication.pdf",{"count":55,"type":21},400,[24],"The goal of this clinical trial is to adapt and implement The Value of Our Health (Our Value), a program to promote eating fruit and vegetables, for people living in rural areas. The program will be offered in small, independent grocery stores and delivered by community health workers. The main question this study will answer is: Do customers who shop at stores receiving Our Value eat more fruits and vegetables than customers of other stores?",[59,60,28,61],"Hispanic Americans","Chronic Disease Prevention","Fruit and Vegetable Consumption",[59,63,61,28,60,64],"Rural Population","Latino Health","2026-04-15",{"date":67,"type":39},"2026-04-20",{"date":69,"type":21},"2026-04-16",{"date":71,"type":21},"2029-05",{"name":73,"class":46},"University of Washington",2,{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":81,"eligibilityCriteria":82,"healthyVolunteers":16,"sex":17,"minAge":83,"maxAge":4,"enrollmentInfo":84,"targetDuration":4,"studyType":22,"phases":86,"briefSummary":87,"conditions":88,"keywords":90,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":103},"100631515","using-middle-school-science-teachers-to-address-cancer-health-disparities-100631515","NCT07501689","Using Middle School Science Teachers to Address Cancer Health Disparities","Using Middle School Science Teachers to Address Health Disparities","CARES4You","Inclusion Criteria:\n\n* Adolescents:\n* Age 10-13\n* Attends a NYC Public Middle School\n* Resides in one of the study's four target PPA's\n* Parents\u002FCaregivers:\n* 18 years of age or older\n* Has at least one child registered for middle school in NYC that resides with them\n* Resides in one of the study's four target PPA's\n* Able to provide informed consent\n\nExclusion Criteria:\n\n* Adolescents: Students who do not attend one of the participating NYC Public Middle Schools\n* Parents\u002FCaregivers: Caregivers who do not have a child that attends one of the participating NYC Public Middle Schools","10 Years",{"count":85,"type":21},1812,[24],"The CARES4You study is testing a middle school science curriculum designed to teach students about cancer risk and prevention. The lessons are taught by regular science teachers during class time and are aligned with national science education standards. The curriculum includes six units (14 lessons) that help students learn about cancer, understand how lifestyle and environmental factors influence risk, and think about ways to make healthy choices.\n\nThe study will take place in 10 public middle schools in New York City. Some schools will begin using the CARES4You curriculum right away, while others will continue with their usual science lessons and receive the program later. Researchers will compare the two groups of schools.\n\nThe main goal of the study is to see whether the curriculum increases students' intentions to engage in healthy behaviors that may reduce cancer risk. The study will also examine whether students talk more with their caregivers about cancer risk and prevention after participating in the program. Caregivers may also report on some health behaviors in the household.\n\nIf the program is effective, CARES4You could provide schools with a practical and sustainable way to teach cancer prevention and promote healthy behaviors among adolescents and their families.",[89,28],"Cancer Risk Factors",[31,91,92,93],"cluster trial","adolescent health","school-based intervention","2026-03-24",{"date":96,"type":39},"2026-03-30",{"date":98,"type":39},"2026-01-29",{"date":100,"type":21},"2028-06-30",{"name":102,"class":46},"Weill Medical College of Cornell University",5,{"id":105,"slug":106,"hasResults":11,"nctId":107,"briefTitle":108,"officialTitle":109,"acronym":110,"eligibilityCriteria":111,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":112,"targetDuration":4,"studyType":22,"phases":114,"briefSummary":115,"conditions":116,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":118,"lastUpdatePostDateStruct":119,"startDateStruct":121,"completionDateStruct":123,"leadSponsor":125,"locationsCount":47},"100630972","behavior-and-risk-awareness-through-video-education-for-firefighters-100630972","NCT07494617","Behavior and Risk Awareness Through Video Education for Firefighters","BRAVE: Behavior and Risk Awareness Through Video Education for Firefighters","BRAVE","Inclusion Criteria:\n\n* Current active career California firefighter\n\nExclusion Criteria:\n\n* None",{"count":113,"type":21},1000,[24],"The goal of this clinical trial is to evaluate the impact of short documentary-style videos to educate and inspire firefighters to take safety measures to prevent cancer incidence and mortality.\n\nThe main question it aims to answer is:\n\nWill firefighters will have a higher perceived susceptibility to cancer, lower perceived barriers to cancer risk reduction practices, and higher perceived self-efficacy and benefit to risk reduction practices after watching the videos?\n\nParticipants will:\n\n* Take a Pre-Intervention survey\n* Watch one of five randomly assigned 5 minute video interventions\n* Take a Post-Intervention survey",[28,117],"Firefighters","2026-03-20",{"date":120,"type":39},"2026-03-27",{"date":122,"type":39},"2025-07-14",{"date":124,"type":21},"2026-07",{"name":126,"class":46},"University of California, Davis",{"id":128,"slug":129,"hasResults":11,"nctId":130,"briefTitle":131,"officialTitle":132,"acronym":4,"eligibilityCriteria":133,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":134,"targetDuration":4,"studyType":22,"phases":136,"briefSummary":137,"conditions":138,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":140,"lastUpdatePostDateStruct":141,"startDateStruct":143,"completionDateStruct":145,"leadSponsor":147,"locationsCount":47},"100610307","eatwell-clinical-trial-r01-100610307","NCT07225881","Eatwell Clinical Trial (R01)","Efficacy of a Multi-level Intervention Designed to Promote Adherence to WCRF\u002FAICR Dietary Guidelines for Cancer Prevention","Inclusion Criteria:\n\n* Age 18 or older\n* Access to technology necessary to receive emails and join videoconferencing meetings\n* Ability to read and speak English\n* Willingness to be randomized to either study condition, including ability and willingness to attend intervention sessions\n* Ability and willingness to attend intervention sessions, receive monthly email messages, and serve in support role if index participant in household is assigned to Eatwell condition\n* Able and willing to visit a commercial laboratory partnered with this project (e.g., Labcorp) in order to have their blood drawn at the time of study visits\n* Low adherence to WCRF\u002FAICR's four dietary guidelines (operationalized as a level of intake, based on brief self-report questions administered during phone screening, that corresponds to a score of 2 or less in the Shams-White method of dietary adherence scoring)\n* Share a household (i.e., a private residence with a shared living space, including kitchen) with an adult who provides informed consent, meets eligibility criteria, and anticipates remaining in this household for the majority of the next 18 months\n* Agree that they will not join another intervention study run by this study team in the next 18 months\n* Successful completion by self and household member of all enrollment and baseline data collection tasks\n* Have an email that they regularly check and willingness to use that for corresponding to study staff\n* Weight at baseline of 396 lbs or less, as the digital scales used for measurement are not able to obtain measurements for weights higher than this\n\nExclusion Criteria:\n\n* A medical or psychiatric condition, including self-reported history of anorexia nervosa or bulimia nervosa, that may limit appropriateness of or ability to comply with dietary recommendations\n* A psychiatric condition, including self-reported history of anorexia nervosa or bulimia nervosa, that may make it difficult or inappropriate for household member to serve in support role\n* Currently taking medication that can substantively change appetite or eating behavior, including using of a GLP-1 medication\n* Planning to enroll in another lifestyle modification program in the next 18 months\n* History of bariatric surgery\n* Currently pregnant or planning to become pregnant in the next 18 months\n* Type 1 Diabetes",{"count":135,"type":21},472,[24],"Cancer is a leading cause of death and will affect many people in their lifetimes. Organizations such as the American Cancer Society and the World Cancer Research Fund\u002FAmerican Institute for Cancer Research (WCRF\u002FAICR) have noted that dietary quality is a key factor influencing cancer risk, but most Americans do not meet these dietary guidelines for cancer prevention. The proposed study will enroll adults from the community (n=236 index participants, 236 household members; N = 472) who have low adherence to WCRF\u002FAICR's four dietary guidelines. Participants will be randomized to either nutrition education or the Eatwell intervention. The Eatwell intervention content is focused on helping participants make healthier grocery shopping decisions, eat at home more often to take advantage of the optimal defaults present there, and learn how to navigate temptation when eating away from home. The findings will be relevant not only to the field of cancer prevention, but to the prevention of other diseases for which dietary quality is important.",[28,139],"Dietary Guidelines","2026-03-13",{"date":142,"type":39},"2026-03-16",{"date":144,"type":39},"2026-02-10",{"date":146,"type":21},"2030-04-30",{"name":148,"class":46},"Drexel University",{"id":150,"slug":151,"hasResults":11,"nctId":152,"briefTitle":153,"officialTitle":154,"acronym":155,"eligibilityCriteria":156,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":157,"targetDuration":4,"studyType":22,"phases":159,"briefSummary":160,"conditions":161,"keywords":163,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":169,"lastUpdatePostDateStruct":170,"startDateStruct":171,"completionDateStruct":173,"leadSponsor":175,"locationsCount":47},"100609832","dietary-fiber-and-time-restricted-eating-100609832","NCT07219706","Dietary Fiber and Time Restricted Eating","Examining the Independent and Combined Effects of Dietary Fiber and Time Restricted Eating on Indicators of Cancer Risk: the Fiber and Time Restricted Eating (F.I.T.) Study","FIBER+TRE","Inclusion Criteria:\n\n* ≥18 age\n* Body mass index ≥30 kg\u002Fm2\n* Dietary fiber intake ≤15 g\u002Fday\n* Compatible cell phone for use of ecological momentary assessment app\n\nExclusion Criteria:\n\n* Self-reported diagnosis that precludes fiber intake (e.g., inflammatory bowel disease)\n* Food allergies or intolerances that limit ability to engage with the intervention\n* Positive screen on the SCOFF eating disorder screener39\n* Current self-reported use of GLP-1 receptor agonists\n* Currently pregnant or breastfeeding, or planning to become pregnant",{"count":158,"type":21},90,[24],"This study is seeking to examine combinations of two different dietary interventions on cancer risk.",[162,28],"Diet Habits",[164,165,166,167,168],"Diet","Weight loss","Fasting","Time restricted eating","Time restricted feeding","2026-03-11",{"date":140,"type":39},{"date":172,"type":21},"2026-12-10",{"date":174,"type":21},"2027-06-30",{"name":176,"class":46},"University of Oklahoma",{"id":178,"slug":179,"hasResults":11,"nctId":180,"briefTitle":181,"officialTitle":182,"acronym":183,"eligibilityCriteria":184,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":185,"targetDuration":4,"studyType":22,"phases":187,"briefSummary":188,"conditions":189,"keywords":196,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":199,"lastUpdatePostDateStruct":200,"startDateStruct":202,"completionDateStruct":204,"leadSponsor":206,"locationsCount":47},"100583958","quitting-matters-human-immunodeficiency-virus-hybrid-trial-100583958","NCT06883097","Quitting Matters Human Immunodeficiency Virus Hybrid Trial","Hybrid Trial of a Digital Therapeutic for Smoking Cessation Among Persons Living With HIV","QMH","Inclusion Criteria:\n\n1. Self-reported daily cigarette smoking over the past 30 days\n2. Self-reported HIV status\n3. Age 18 or older\n4. Desire to quit smoking\n5. Willing and medically eligible to use NRT\n6. Currently receiving HIV care\n7. Currently owning an Android or iOS smartphone\n\nExclusion Criteria:\n\n1. Current acute psychotic episode or unsafe to participate in the study\n2. Pregnant or intending to become pregnant in the next 6 months\n3. Currently receiving any pharmacological and\u002For behavioral intervention or counseling for smoking cessation\n4. Any medical condition or medication that could compromise subject safety, as determined by the PIs and\u002For study physician\n5. Not able to fluently speak and write in English\n6. Hearing, comprehension, visual, speech, or motor limitations that preclude study participation",{"count":186,"type":21},314,[24],"The purpose of this study is to compare the advantages and disadvantages of two approaches for quitting smoking among people living with HIV (PWH). Participants will complete a 24- week (\\~6-month) study where the Participants will be assigned to one of two smartphone apps to help with quitting smoking. Regardless of the group participants are assigned to, they will also receive a combination of nicotine replacement therapy (patches and gums) that have been shown to help people quit smoking. The main questions this study aims to answer are:\n\nParticipants will complete 5 video call visits over about 6 months. Participants will install their assigned smoking cessation app onto their phone and will be asked to use the app for the duration of the study along with their provided Nicotine Replacement Therapy (NRT) products. During the study visits, participants will meet with study staff to complete questionnaires and interviews. Participants may be asked to provide breath and saliva samples to measure the level of carbon monoxide and nicotine.",[190,191,192,193,194,195,28],"Tobacco","Tobacco Abstinence","Smoking Cessation","Smoking Cessation; Tobacco Dependence","Human Immunodeficiency Virus (HIV)","Tobacco Dependence Caused by Cigarettes",[190,192,197,191,198],"Human immunodeficiency virus (HIV)","Quit Smoking","2025-12-15",{"date":201,"type":39},"2025-12-17",{"date":203,"type":39},"2025-08-18",{"date":205,"type":21},"2028-12",{"name":207,"class":46},"Wake Forest University Health Sciences",{"id":209,"slug":210,"hasResults":11,"nctId":211,"briefTitle":212,"officialTitle":213,"acronym":214,"eligibilityCriteria":215,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":216,"targetDuration":4,"studyType":22,"phases":218,"briefSummary":219,"conditions":220,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":224,"lastUpdatePostDateStruct":225,"startDateStruct":227,"completionDateStruct":229,"leadSponsor":231,"locationsCount":47},"100548463","personalised-health-recommendations-to-the-general-population-through-an-integrated-ai-guided-100548463","NCT06421324","Personalised Health Recommendations to the General Population Through an Integrated AI Guided","Interventional Study Focused on Providing Personalised Health Recommendations to the General Population Through an Integrated AI Guided App as a Strategy for Gastric Cancer Prevention (AIDA)","AIDA","Inclusion Criteria:\n\n* Subjects ≥ 18 years old with a diagnosis of GIM or previous or current H. pylori infection, to whom a gastroscopy is indicated within clinical care\n* Availability of a signed informed consent form to participate in the study\n\nExclusion Criteria:\n\n* Patients to whom an endoscopy is performed for the follow-up of another illness such as oesophageal varices and\u002For for therapy such as endoscopic dilation, feeding tube placement or endoscopic resection\n* Subjects with a clinical diagnosis of gastric diseases other than GIM or GC\n* Patients who have received antimicrobials during the four weeks prior to the endoscopy\n* Patients who have received proton pump inhibitors and\u002For bismuth-based treatments at least two weeks prior to the endoscopy\n* Subjects for whom clinical data are not available: H. pylori status, eradication treatment, sex, age, tobacco smoking, and first-degree family history of gastric cancer\n* Subjects who lack the mental capacity to understand the nature and requirements of the study and who lack the ability to give informed consent",{"count":217,"type":21},450,[24],"This clinical study aims to be used to implement and validate the AIDA tool in two phases:\n\n* Phase 1: Risk stratification and personalised recommendations \\& Model development\n* Phase 2: Mechanistic Model (Bioresource) development \\& testing",[221,28,222,223],"Gastric Cancer","Helicobacter Pylori Infection","Artificial Intelligence","2025-02-25",{"date":226,"type":39},"2025-02-27",{"date":228,"type":39},"2024-06-01",{"date":230,"type":21},"2026-12-31",{"name":232,"class":46},"Fundación para la Investigación del Hospital Clínico de Valencia"]