[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"polygenic-risk-score\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:polygenic-risk-score":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":29,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100620504","delphi-procedure-for-developing-recommendations-for-the-implementation-of-wearable-devices-and-polygenic-risk-scores-100620504",false,"NCT07358481","DELphi Procedure for Developing Recommendations for the Implementation of Wearable Devices and Polygenic Risk Scores","DEL-DIP: DELphi Procedure for Developing Recommendations for the Implementation of Wearable Devices and Polygenic Risk Scores","DEL-DIP","Inclusion criteria\n\n* Experts in cardiology\n* Experts in personalized medicine\n* Experts in digital health.\n\nExclusion criteria\n\n\\- Failure to provide informed consent (i.e., non-acceptance of the informed consent form)",true,"ALL",{"count":20,"type":21},10,"ESTIMATED","OBSERVATIONAL","DEL-DIP is a prospective observational study employing a Delphi methodology (at least two online rounds) to elicit and consolidate the views of an expert panel within the INNOPREV project. The study aims to develop operational recommendations to support the coordinated implementation of Polygenic Risk Scores (PRS) and wearable devices in cardiovascular prevention. Specifically, it addresses the following research question: which recommendations and requirements-genomic, digital, and clinical\u002Forganizational-are necessary to integrate PRS and wearable technologies into routine practice and healthcare services, and for which of these elements do experts achieve consensus (defined as a Content Validity Index, CVI, \\> 79%)",[25,26,27,28],"Wearable Electronic Devices","Polygenic Risk Score","CVD - Cardiovascular Disease","Primary Prevention",[30],"cardiovascular prevention","NOT_YET_RECRUITING","2026-01-22",{"date":34,"type":35},"2026-01-23","ACTUAL",{"date":37,"type":21},"2026-02",{"date":39,"type":21},"2026-04",{"name":41,"class":42},"Fondazione Policlinico Universitario Agostino Gemelli IRCCS","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":17,"sex":51,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":56,"phases":57,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":75},"100546722","polygenic-risk-stratification-combined-with-mpmri-to-identify-clinically-relevant-prostate-cancer-100546722","NCT06398639","Polygenic Risk Stratification Combined With mpMRI to Identify Clinically Relevant Prostate Cancer","PRS","Inclusion Criteria:\n\n* They must have the ability to understand and the willingness to sign a written information consent document.\n* Estimated life expectancy of greater than 10 years.\n* No history of prostate cancer.\n* Participants must be between 40-69 years of age. This is the age at which screening for prostate cancer is recommended. This is due to younger patients not being at risk for the disease and older patients not benefiting from diagnosis.\n* No biopsy for prostate cancer within the past 5 years.\n* No prostate MRI within the past 5 years.\n\nExclusion Criteria:\n\n* Unwillingness to sign the informed consent form.\n* Contraindication to biopsy such as uncorrectable bleeding or coagulation disorder.\n* Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness\u002Fsocial situations that would limit the safety of a biopsy and\u002For surgery.\n* Unable to undergo an MRI.","MALE","40 Years","69 Years",{"count":55,"type":21},1500,"INTERVENTIONAL",[58],"NA","The goal of this clinical trial is to evaluate a screening method to detect clinically relevant prostate cancer. This clinical trial is using genetic data to determine a man's risk of cancer, together with multiparametric magnetic resonance imaging (mpMRI) to identify men with higher grade cancer.\n\nThe main questions it aims to answer are:\n\n* If genetic data related to prostate cancer used with MRI can identify higher-grade, potentially fatal prostate cancer\n* What age a MRI is useful clinically for prostate cancer screening\n* If deep learning methods used with MRI when the genetic risk of the man is known can more accurately predict significant cancers\n\nParticipants will:\n\n* Get a prostate specific antigen (PSA) blood test\n* Get an mpMRI\n* Get the results of their genetic data to determine if they are considered high-, intermediate-, or low-risk for prostate cancer based on the trials genetic testing\n* Follow-up for this trial based on the participants risk and findings from the PSA test and mpMRI",[61,26],"Prostate Cancer",[26,61,63,64],"Prostate Cancer Screening","Multiparametric MRI","RECRUITING","2025-11-06",{"date":68,"type":35},"2025-11-10",{"date":70,"type":35},"2024-05-07",{"date":72,"type":21},"2030-04-30",{"name":74,"class":42},"Adam S. Kibel, MD",5]