[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100637127":3},{"organization":4,"outcomesModule":7,"designInfo":14,"detailedDescription":20,"studyPopulation":13,"armGroups":21,"interventions":32,"overallOfficials":37,"centralContacts":41,"locations":46,"responsibleParty":65,"collaborators":13,"id":67,"slug":13,"hasResults":68,"nctId":69,"briefTitle":70,"officialTitle":70,"acronym":13,"eligibilityCriteria":71,"healthyVolunteers":68,"sex":72,"minAge":73,"maxAge":13,"enrollmentInfo":74,"targetDuration":13,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":13,"overallStatus":49,"whyStopped":13,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":92},{"fullName":5,"class":6},"M.D. Anderson Cancer Center","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":13},[9],{"measure":10,"description":11,"timeFrame":12},"Safety and Adverse Events (AEs)","Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0","Through study completion; an average of 1 year",null,{"allocation":15,"interventionModel":16,"interventionModelDescription":13,"primaryPurpose":17,"observationalModel":13,"timePerspective":13,"maskingInfo":18},"NON_RANDOMIZED","PARALLEL","HEALTH_SERVICES_RESEARCH",{"masking":19,"maskingDescription":13,"whoMasked":13},"NONE","Primary Objectives:\n\nThe study objective is to increase the number of participants on prostate cancer clinical trials at LBJ. Investigators will complete several objectives:\n\n* To design a culturally tailored video highlighting participant narratives and determine its impact on participants' decision-making pertaining to joining a clinical trial\n* To conduct educational sessions with frontline oncology providers\n* To coordinate participant care through utilization of a nurse navigator\n* To evaluate the effectiveness of this multi-pronged intervention to increase enrollment onto two prostate cancer clinical trials and compare enrollment and one-year retention rates before and after the intervention",[22,28],{"label":23,"type":24,"description":25,"interventionNames":26},"Video Intervention to Prostate Cancer Patient","EXPERIMENTAL","The interventions will be conducted at Lyndon B. Johnson (LBJ) Hospital, a safety net facility that cares for a majority Latino and\u002For Black patient population.",[27],"Other: Video",{"label":29,"type":24,"description":30,"interventionNames":31},"To Conduct Educational Sessions with Frontline Oncology Providers","The investigator will conduct multiple one-hour educational sessions focused on participant-centered communication and cultural competency with the 42 oncology fellows during their academic half-days. Fellows attending the educational sessions will be invited to complete a Likert-style course evaluation form and provide open-ended feedback.\"",[27],[33],{"type":6,"name":34,"description":35,"armGroupLabels":36,"otherNames":13},"Video","Participants will watch a short video in clinic. Participants will complete the two validated scales before and after viewing the video.",[29,23],[38],{"name":39,"affiliation":5,"role":40},"Debanjan Pain, MD","PRINCIPAL_INVESTIGATOR",[42],{"name":39,"role":43,"phone":44,"phoneExt":13,"email":45},"CONTACT","(713) 745-0075","dpain@mdanderson.org",[47],{"facility":48,"status":49,"city":50,"state":51,"zip":52,"country":53,"countryCode":54,"cosmosGeoPoint":55,"geoPoint":60,"contacts":61},"The University of Texas M. D. Anderson Cancer Center","RECRUITING","Houston","Texas","77090","United States","US",{"type":56,"coordinates":57},"Point",[58,59],-95.36327,29.76328,{"lat":59,"lon":58},[62,64],{"name":39,"role":43,"phone":63,"phoneExt":13,"email":45},"713-745-0075",{"name":39,"role":40,"phone":13,"phoneExt":13,"email":13},{"type":66,"investigatorFullName":13,"investigatorTitle":13,"investigatorAffiliation":13,"oldNameTitle":13,"oldOrganization":13},"SPONSOR","100637127",false,"NCT07591701","Efforts to Increase Representation in Prostate Cancer Clinical Trials at Lyndon B. Johnson Hospital","Inclusion Criteria:\n\nThese criteria include diagnosed prostate cancer patients receiving care at LBJ Hospital who\n\nAre eligible for an open prostate cancer clinical trial at LBJ Hospital during the study period\n\nCan provide informed consent.\n\nExclusion Criteria:\n\nThese criteria include prostate cancer patients receiving care at LBJ who are unable to participate due to a serious psychological or cognitive condition or have a medical condition that prevents participation in the trial.","MALE","18 Years",{"count":75,"type":76},60,"ESTIMATED","INTERVENTIONAL",[79],"NA","The main rationale underlying this study is that prostate cancer clinical trials are lacking representation from racial and ethnic minority groups. Study proposal aims to target barriers at the participant, investigator, and health system level through specific interventions to increase the percentage of participants from these backgrounds on cancer clinical trials.",[82],"Prostate Cancer","2026-06-23",{"date":85,"type":86},"2026-06-26","ACTUAL",{"date":88,"type":86},"2026-05-26",{"date":90,"type":76},"2030-01-31",{"name":5,"class":6},1]